{"title":"Oncology Signaling — ELISA Kits","description":null,"products":[{"product_id":"human-p53-elisa-kit-picokine-bhe21000679","title":"Human P53 ELISA Kit PicoKine®","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eAlso known as:\u003c\/strong\u003e Cellular tumor antigen p53, TP53.\u003c\/p\u003e\u003cp\u003eHuman \u003cstrong\u003eP53\u003c\/strong\u003e (\u003cstrong\u003eTP53\u003c\/strong\u003e) is a commonly measured biological analyte that can provide insight into cellular state and tissue physiology. This target is frequently investigated in \u003cstrong\u003eMolecular \u0026amp; Cellular Biology\u003c\/strong\u003e research contexts. As with many protein targets, abundance can be influenced by transcriptional regulation, secretion or shedding, proteolytic processing, and clearance. Quantitative measurement is often used to connect molecular changes with phenotypes such as stress responses, immune activation, differentiation, or tissue remodeling.\u003c\/p\u003e\u003ch2\u003eBiological context and interpretation\u003c\/h2\u003e\u003cp\u003eProtein-level readouts complement nucleic-acid measurements by reflecting post-transcriptional control and protein stability. Depending on the model system, changes may be transient or sustained, and may represent direct pathway engagement or secondary effects. When interpreting results, consider sample matrix effects, timing relative to stimulation or treatment, and whether complexes or modified forms of the analyte may be present.\u003c\/p\u003e\u003ch2\u003eWhy it matters in research\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eComparative quantification:\u003c\/strong\u003e Supports analysis across experimental groups, time points, or dose ranges.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePathway context:\u003c\/strong\u003e Useful as part of a broader marker panel to triangulate biological mechanisms.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eModel characterization:\u003c\/strong\u003e Helps profile baseline vs perturbed states in cells, tissues, or biofluids.\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eRelated pathways and interacting partners\u003c\/h2\u003e\u003cp\u003eFor many targets, interpretability improves when measured alongside biologically connected markers (e.g., upstream regulators, downstream effectors, and cell-type indicators). Designing panels around a pathway hypothesis can help distinguish primary pathway activation from general stress or inflammation.\u003c\/p\u003e","brand":"Boster Bio","offers":[{"title":"96 wells\/kit, with removable strips.","offer_id":52920824562029,"sku":"EK0895","price":499.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/ek0895.png?v=1769077800"},{"product_id":"human-cyclin-dependent-kinase-1-cdk-1-elisa-kit-bhe12102444","title":"Human Cyclin-dependent Kinase 1, CDK-1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase 1 (CDK1)\u003c\/strong\u003e is a molecular target commonly studied in life science research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P06493\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Cyclin-dependent Kinase 1 (CDK1) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Cyclin-dependent Kinase 1 (CDK1) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eCyclin-dependent Kinase 1 (CDK1) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Cyclin-dependent Kinase 1 (CDK1) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase 1 (CDK1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCDK 1\u003c\/strong\u003e, \u003cstrong\u003eCDK1\u003c\/strong\u003e, and \u003cstrong\u003eCell division control protein 2 homolog\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952462066029,"sku":"E0765Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0765Hu.jpg?v=1769146078"},{"product_id":"human-cyclin-dependent-like-kinase-5-cdk-5-elisa-kit-bhe12102460","title":"Human Cyclin-dependent-like Kinase 5, CDK-5 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent-like Kinase 5 (CDK5)\u003c\/strong\u003e is a molecular target commonly studied in cell biology, neuroscience, and cancer research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q00535\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Cyclin-dependent-like Kinase 5 (CDK5) is frequently examined in relation to signal transduction pathways, cell cycle and stress-response programs, and organelle and membrane dynamics. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Cyclin-dependent-like Kinase 5 (CDK5) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eCyclin-dependent-like Kinase 5 (CDK5) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Cyclin-dependent-like Kinase 5 (CDK5) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent-like Kinase 5 (CDK5)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCDK 5\u003c\/strong\u003e, \u003cstrong\u003eCDK5\u003c\/strong\u003e, and \u003cstrong\u003eCell division protein kinase 5\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952462328173,"sku":"E0781Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0781Hu.jpg?v=1769146081"},{"product_id":"human-cyclin-dependent-kinase-4-cdk-4-elisa-kit-bhe12102545","title":"Human Cyclin-dependent Kinase 4, CDK-4 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase 4 (CDK4)\u003c\/strong\u003e is a molecular target commonly studied in cell biology research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P11802\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Cyclin-dependent Kinase 4 (CDK4) is frequently examined in relation to signal transduction pathways, cell cycle and stress-response programs, and organelle and membrane dynamics. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Cyclin-dependent Kinase 4 (CDK4) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eCyclin-dependent Kinase 4 (CDK4) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Cyclin-dependent Kinase 4 (CDK4) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase 4 (CDK4)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCDK 4\u003c\/strong\u003e, \u003cstrong\u003eCDK4\u003c\/strong\u003e, and \u003cstrong\u003eCell division protein kinase 4\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952462917997,"sku":"E0870Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0870Hu.jpg?v=1769146090"},{"product_id":"human-mitogen-activited-protein-kinase1-mapk1-elisa-kit-bhe12102548","title":"Human Mitogen Activited Protein Kinase1, MAPK1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eMitogen Activited Protein Kinase1 (MAPK1)\u003c\/strong\u003e is a molecular target commonly studied in life science research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P28482\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Mitogen Activited Protein Kinase1 (MAPK1) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Mitogen Activited Protein Kinase1 (MAPK1) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eMitogen Activited Protein Kinase1 (MAPK1) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Mitogen Activited Protein Kinase1 (MAPK1) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eMitogen Activited Protein Kinase1 (MAPK1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eERK-2\u003c\/strong\u003e, \u003cstrong\u003eERT1\u003c\/strong\u003e, and \u003cstrong\u003eExtracellular signal-regulated kinase 2\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952462950765,"sku":"E0873Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0873Hu.jpg?v=1769146091"},{"product_id":"human-cyclin-dependent-kinase-2-cdk-2-elisa-kit-bhe12102626","title":"Human Cyclin-dependent Kinase 2, CDK-2 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase 2 (CDK2)\u003c\/strong\u003e is a molecular target commonly studied in cancer research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P24941\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Cyclin-dependent Kinase 2 (CDK2) is frequently examined in relation to tumor microenvironment biology, cell proliferation and apoptosis, and angiogenesis and immune-oncology mechanisms. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Cyclin-dependent Kinase 2 (CDK2) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eCyclin-dependent Kinase 2 (CDK2) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Cyclin-dependent Kinase 2 (CDK2) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase 2 (CDK2)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCDK 2\u003c\/strong\u003e, \u003cstrong\u003eCDK2\u003c\/strong\u003e, and \u003cstrong\u003eCell division protein kinase 2\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952463769965,"sku":"E0952Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0952Hu.jpg?v=1769146101"},{"product_id":"human-g1-s-specific-cyclin-d1-cyclin-d1-elisa-kit-bhe12103221","title":"Human G1\/S-specific Cyclin-D1, CYCLIN-D1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eG1\/S-specific Cyclin-D1 (CCND1)\u003c\/strong\u003e is a molecular target commonly studied in life science research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P24385\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, G1\/S-specific Cyclin-D1 (CCND1) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of G1\/S-specific Cyclin-D1 (CCND1) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eG1\/S-specific Cyclin-D1 (CCND1) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of G1\/S-specific Cyclin-D1 (CCND1) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eG1\/S-specific Cyclin-D1 (CCND1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eB-cell lymphoma 1 protein\u003c\/strong\u003e, \u003cstrong\u003eBCL-1\u003c\/strong\u003e, and \u003cstrong\u003eBCL-1 oncogene\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952471306605,"sku":"E1636Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E1636Hu.jpg?v=1769146146"},{"product_id":"human-adenomatosis-polyposis-coli-protein-apc-elisa-kit-bhe12103824","title":"Human Adenomatosis Polyposis Coli Protein, APC ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eAdenomatosis Polyposis Coli Protein (APC)\u003c\/strong\u003e is a molecular target commonly studied in life science research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P25054\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Adenomatosis Polyposis Coli Protein (APC) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Adenomatosis Polyposis Coli Protein (APC) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eAdenomatosis Polyposis Coli Protein (APC) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Adenomatosis Polyposis Coli Protein (APC) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eAdenomatosis Polyposis Coli Protein (APC)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eAdenomatous polyposis coli protein\u003c\/strong\u003e, \u003cstrong\u003eAPC\u003c\/strong\u003e, and \u003cstrong\u003eDeleted in polyposis 2.5\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952478286189,"sku":"E2284Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2284Hu.jpg?v=1769146204"},{"product_id":"human-protein-wnt-4-wnt4-elisa-kit-bhe12103889","title":"Human Protein Wnt-4, WNT4 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProtein Wnt-4 (WNT4)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction, stem cells, and cancer research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P56705\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Protein Wnt-4 (WNT4) is frequently examined in relation to tumor microenvironment biology, cell proliferation and apoptosis, and angiogenesis and immune-oncology mechanisms. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Protein Wnt-4 (WNT4) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eProtein Wnt-4 (WNT4) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Protein Wnt-4 (WNT4) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProtein Wnt-4 (WNT4)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eProtein Wnt-4\u003c\/strong\u003e, \u003cstrong\u003eSERKAL\u003c\/strong\u003e, and \u003cstrong\u003eWNT4\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952480186733,"sku":"E2351Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2351Hu.jpg?v=1769146219"},{"product_id":"human-protein-wnt-2-wnt2-elisa-kit-bhe12103894","title":"Human Protein Wnt-2, WNT2 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProtein Wnt-2 (WNT2)\u003c\/strong\u003e is a molecular target commonly studied in stem cells research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P09544\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Protein Wnt-2 (WNT2) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Protein Wnt-2 (WNT2) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eProtein Wnt-2 (WNT2) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Protein Wnt-2 (WNT2) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProtein Wnt-2 (WNT2)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eInt-1-like protein 1\u003c\/strong\u003e, \u003cstrong\u003eInt-1-related protein\u003c\/strong\u003e, and \u003cstrong\u003eIRP\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952480317805,"sku":"E2356Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2356Hu.jpg?v=1769146220"},{"product_id":"human-frizzled-5-fzd5-elisa-kit-bhe12103900","title":"Human Frizzled-5, FZD5 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-5 (FZD5)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q13467\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Frizzled-5 (FZD5) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Frizzled-5 (FZD5) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eFrizzled-5 (FZD5) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Frizzled-5 (FZD5) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-5 (FZD5)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eC2orf31\u003c\/strong\u003e, \u003cstrong\u003eFrizzled-5\u003c\/strong\u003e, and \u003cstrong\u003eFz-5\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952480383341,"sku":"E2362Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2362Hu.jpg?v=1769146220"},{"product_id":"human-frizzled-7-fzd7-elisa-kit-bhe12103901","title":"Human Frizzled-7, FZD7 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-7 (FZD7)\u003c\/strong\u003e is a molecular target commonly studied in life science research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: O75084\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Frizzled-7 (FZD7) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Frizzled-7 (FZD7) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eFrizzled-7 (FZD7) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Frizzled-7 (FZD7) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-7 (FZD7)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eFrizzled-7\u003c\/strong\u003e, \u003cstrong\u003eFz-7\u003c\/strong\u003e, and \u003cstrong\u003eFZD7\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952480416109,"sku":"E2363Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2363Hu.jpg?v=1769146221"},{"product_id":"human-frizzled-4-fzd4-elisa-kit-bhe12103902","title":"Human Frizzled-4, FZD4 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-4 (FZD4)\u003c\/strong\u003e is a molecular target commonly studied in life science research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q9ULV1\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Frizzled-4 (FZD4) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Frizzled-4 (FZD4) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eFrizzled-4 (FZD4) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Frizzled-4 (FZD4) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-4 (FZD4)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCD antigen CD344\u003c\/strong\u003e, \u003cstrong\u003eCD344\u003c\/strong\u003e, and \u003cstrong\u003eEVR1\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952480448877,"sku":"E2364Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2364Hu.jpg?v=1769146221"},{"product_id":"human-frizzled-10-fzd10-elisa-kit-bhe12103903","title":"Human Frizzled-10, FZD10 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-10 (FZD10)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q9ULW2\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Frizzled-10 (FZD10) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Frizzled-10 (FZD10) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eFrizzled-10 (FZD10) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Frizzled-10 (FZD10) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-10 (FZD10)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCD antigen CD350\u003c\/strong\u003e, \u003cstrong\u003eCD350\u003c\/strong\u003e, and \u003cstrong\u003eFrizzled-10\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952480481645,"sku":"E2365Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2365Hu.jpg?v=1769146221"},{"product_id":"human-frizzled-9-fzd9-elisa-kit-bhe12103904","title":"Human Frizzled-9, FZD9 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-9 (FZD9)\u003c\/strong\u003e is a molecular target commonly studied in life science research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: O00144\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Frizzled-9 (FZD9) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Frizzled-9 (FZD9) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eFrizzled-9 (FZD9) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Frizzled-9 (FZD9) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-9 (FZD9)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCD antigen CD349\u003c\/strong\u003e, \u003cstrong\u003eCD349\u003c\/strong\u003e, and \u003cstrong\u003eFrizzled-9\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952480514413,"sku":"E2366Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2366Hu.jpg?v=1769146222"},{"product_id":"human-frizzled-6-fzd6-elisa-kit-bhe12103905","title":"Human Frizzled-6, FZD6 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-6 (FZD6)\u003c\/strong\u003e is a molecular target commonly studied in life science research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: O60353\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Frizzled-6 (FZD6) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Frizzled-6 (FZD6) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eFrizzled-6 (FZD6) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Frizzled-6 (FZD6) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-6 (FZD6)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eFrizzled-6\u003c\/strong\u003e, \u003cstrong\u003eFZ6\u003c\/strong\u003e, and \u003cstrong\u003eFZ-6\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952480547181,"sku":"E2367Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2367Hu.jpg?v=1769146222"},{"product_id":"human-frizzled-1-fzd1-elisa-kit-bhe12103906","title":"Human Frizzled-1, FZD1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-1 (FZD1)\u003c\/strong\u003e is a molecular target commonly studied in life science research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q9UP38\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Frizzled-1 (FZD1) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Frizzled-1 (FZD1) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eFrizzled-1 (FZD1) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Frizzled-1 (FZD1) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-1 (FZD1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eFrizzled-1\u003c\/strong\u003e, \u003cstrong\u003eFz-1\u003c\/strong\u003e, and \u003cstrong\u003eFZD 1\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952480579949,"sku":"E2368Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2368Hu.jpg?v=1769146222"},{"product_id":"human-frizzled-2-fzd2-elisa-kit-bhe12103907","title":"Human Frizzled-2, FZD2 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-2 (FZD2)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q14332\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Frizzled-2 (FZD2) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Frizzled-2 (FZD2) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eFrizzled-2 (FZD2) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Frizzled-2 (FZD2) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-2 (FZD2)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eFrizzled-2\u003c\/strong\u003e, \u003cstrong\u003eFz-2\u003c\/strong\u003e, and \u003cstrong\u003eFZD 2\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952480612717,"sku":"E2369Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2369Hu.jpg?v=1769146223"},{"product_id":"human-frizzled-3-fzd3-elisa-kit-bhe12103908","title":"Human Frizzled-3, FZD3 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-3 (FZD3)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q9NPG1\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Frizzled-3 (FZD3) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Frizzled-3 (FZD3) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eFrizzled-3 (FZD3) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Frizzled-3 (FZD3) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eFrizzled-3 (FZD3)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eFrizzled-3\u003c\/strong\u003e, \u003cstrong\u003eFz-3\u003c\/strong\u003e, and \u003cstrong\u003eFZD3\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952480645485,"sku":"E2370Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2370Hu.jpg?v=1769146223"},{"product_id":"human-catenin-beta-1-ctnnb1-elisa-kit-bhe12103934","title":"Human Catenin Beta 1, CTNNB1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCatenin Beta 1 (CTNNB1)\u003c\/strong\u003e is a molecular target commonly studied in cardiovascular research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P35222\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Catenin Beta 1 (CTNNB1) is frequently examined in relation to vascular biology and endothelial function, cardiac remodeling and injury responses, and hemostasis and thrombosis. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Catenin Beta 1 (CTNNB1) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eCatenin Beta 1 (CTNNB1) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Catenin Beta 1 (CTNNB1) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCatenin Beta 1 (CTNNB1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eBeta-catenin\u003c\/strong\u003e, \u003cstrong\u003eCatenin beta-1\u003c\/strong\u003e, and \u003cstrong\u003eCTNNB 1\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952481431917,"sku":"E2396Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2396Hu.jpg?v=1769146229"},{"product_id":"human-dual-specificity-mitogen-activated-protein-kinase-1-map2k1-elisa-kit-bhe12104026","title":"Human Dual Specificity Mitogen-activated Protein Kinase 1, MAP2K1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eDual Specificity Mitogen-activated Protein Kinase 1 (MAP2K1)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q02750\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Dual Specificity Mitogen-activated Protein Kinase 1 (MAP2K1) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Dual Specificity Mitogen-activated Protein Kinase 1 (MAP2K1) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eDual Specificity Mitogen-activated Protein Kinase 1 (MAP2K1) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Dual Specificity Mitogen-activated Protein Kinase 1 (MAP2K1) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eDual Specificity Mitogen-activated Protein Kinase 1 (MAP2K1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCFC3\u003c\/strong\u003e, \u003cstrong\u003eDual specificity mitogen-activated protein kinase 1\u003c\/strong\u003e, and \u003cstrong\u003eERK activator kinase 1\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952483365229,"sku":"E2488Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2488Hu.jpg?v=1769146244"},{"product_id":"human-glycogen-synthase-kinase-3-alpha-gsk3a-elisa-kit-bhe12104724","title":"Human Glycogen Synthase Kinase-3 Alpha, GSK3A ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eGlycogen Synthase Kinase-3 Alpha (GSK3A)\u003c\/strong\u003e is a molecular target commonly studied in cell biology research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P49840\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Glycogen Synthase Kinase-3 Alpha (GSK3A) is frequently examined in relation to signal transduction pathways, cell cycle and stress-response programs, and organelle and membrane dynamics. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Glycogen Synthase Kinase-3 Alpha (GSK3A) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eGlycogen Synthase Kinase-3 Alpha (GSK3A) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Glycogen Synthase Kinase-3 Alpha (GSK3A) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eGlycogen Synthase Kinase-3 Alpha (GSK3A)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eGlycogen Synthase kinase-3 alpha\u003c\/strong\u003e, \u003cstrong\u003eGSK 3A\u003c\/strong\u003e, and \u003cstrong\u003eGSK-3 alpha\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952498602349,"sku":"E3195Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E3195Hu.jpg?v=1769146383"},{"product_id":"human-glycogen-synthase-kinase-3-beta-gsk3b-elisa-kit-bhe12104725","title":"Human Glycogen Synthase Kinase-3 Beta, GSK3B ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eGlycogen Synthase Kinase-3 Beta (GSK3B)\u003c\/strong\u003e is a molecular target commonly studied in life science research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P49841\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Glycogen Synthase Kinase-3 Beta (GSK3B) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Glycogen Synthase Kinase-3 Beta (GSK3B) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eGlycogen Synthase Kinase-3 Beta (GSK3B) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Glycogen Synthase Kinase-3 Beta (GSK3B) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eGlycogen Synthase Kinase-3 Beta (GSK3B)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eGlycogen Synthase kinase-3 beta\u003c\/strong\u003e, \u003cstrong\u003eGSK 3B\u003c\/strong\u003e, and \u003cstrong\u003eGSK-3 beta\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952498667885,"sku":"E3196Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E3196Hu.jpg?v=1769146384"},{"product_id":"human-phosphatidylinositol-3-4-5-trisphosphate-3-phosphatase-and-dual-specificity-protein-phosphatase-pten-pten-elisa-kit-bhe12104771","title":"Human Phosphatidylinositol-3,4, 5-Trisphosphate 3-phosphatase and Dual-specificity Protein Phosphatase Pten, PTEN ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ePhosphatidylinositol-3, 4, 5-Trisphosphate 3-phosphatase and Dual-specificity Protein Phosphatase Pten (PTEN)\u003c\/strong\u003e is a molecular target commonly studied in cell biology, signal transduction, and epigenetics and nuclear signaling research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P60484\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Phosphatidylinositol-3, 4, 5-Trisphosphate 3-phosphatase and Dual-specificity Protein Phosphatase Pten (PTEN) is frequently examined in relation to signal transduction pathways, cell cycle and stress-response programs, and organelle and membrane dynamics. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Phosphatidylinositol-3, 4, 5-Trisphosphate 3-phosphatase and Dual-specificity Protein Phosphatase Pten (PTEN) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003ePhosphatidylinositol-3, 4, 5-Trisphosphate 3-phosphatase and Dual-specificity Protein Phosphatase Pten (PTEN) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Phosphatidylinositol-3, 4, 5-Trisphosphate 3-phosphatase and Dual-specificity Protein Phosphatase Pten (PTEN) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ePhosphatidylinositol-3, 4, 5-Trisphosphate 3-phosphatase and Dual-specificity Protein Phosphatase Pten (PTEN)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003e10q23del\u003c\/strong\u003e, \u003cstrong\u003eBZS\u003c\/strong\u003e, and \u003cstrong\u003eCWS1\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952499716461,"sku":"E3242Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E3242Hu.jpg?v=1769146394"},{"product_id":"human-cyclin-dependent-kinase-inhibitor-1-cdkn1a-elisa-kit-bhe12104772","title":"Human Cyclin-dependent Kinase Inhibitor 1, CDKN1A ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase Inhibitor 1 (CDKN1A)\u003c\/strong\u003e is a molecular target commonly studied in life science research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P38936\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Cyclin-dependent Kinase Inhibitor 1 (CDKN1A) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Cyclin-dependent Kinase Inhibitor 1 (CDKN1A) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eCyclin-dependent Kinase Inhibitor 1 (CDKN1A) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Cyclin-dependent Kinase Inhibitor 1 (CDKN1A) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase Inhibitor 1 (CDKN1A)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCDK-interacting protein 1\u003c\/strong\u003e, \u003cstrong\u003eCDKN1A\u003c\/strong\u003e, and \u003cstrong\u003eCyclin-dependent kinase inhibitor 1\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952499749229,"sku":"E3243Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E3243Hu.jpg?v=1769146394"},{"product_id":"human-mitogen-activited-protein-kinase-3-mapk3-elisa-kit-bhe12104780","title":"Human Mitogen Activited Protein Kinase 3, MAPK3 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eMitogen Activited Protein Kinase 3 (MAPK3)\u003c\/strong\u003e is a molecular target commonly studied in life science research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P27361\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Mitogen Activited Protein Kinase 3 (MAPK3) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Mitogen Activited Protein Kinase 3 (MAPK3) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eMitogen Activited Protein Kinase 3 (MAPK3) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Mitogen Activited Protein Kinase 3 (MAPK3) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eMitogen Activited Protein Kinase 3 (MAPK3)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eERK-1\u003c\/strong\u003e, \u003cstrong\u003eERT2\u003c\/strong\u003e, and \u003cstrong\u003eExtracellular signal-regulated kinase 1\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952499945837,"sku":"E3251Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E3251Hu.jpg?v=1769146397"},{"product_id":"human-rapamycin-insensitive-companion-of-mtor-rictor-elisa-kit-bhe12105070","title":"Human Rapamycin Insensitive Companion of Mtor, RICTOR ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eRapamycin Insensitive Companion of Mtor (RICTOR)\u003c\/strong\u003e is a molecular target commonly studied in cell biology research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q6R327\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Rapamycin Insensitive Companion of Mtor (RICTOR) is frequently examined in relation to signal transduction pathways, cell cycle and stress-response programs, and organelle and membrane dynamics. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Rapamycin Insensitive Companion of Mtor (RICTOR) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eRapamycin Insensitive Companion of Mtor (RICTOR) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Rapamycin Insensitive Companion of Mtor (RICTOR) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eRapamycin Insensitive Companion of Mtor (RICTOR)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eAVO3\u003c\/strong\u003e, \u003cstrong\u003eAVO3 homolog\u003c\/strong\u003e, and \u003cstrong\u003ehAVO3\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952506335597,"sku":"E3592Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E3592Hu.jpg?v=1769146452"},{"product_id":"human-ribosomal-protein-s6-kinase-beta-1-rps6kb1-elisa-kit-bhe12105178","title":"Human Ribosomal Protein S6 Kinase Beta-1, RPS6KB1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eRibosomal Protein S6 Kinase Beta-1 (RPS6KB1)\u003c\/strong\u003e is a molecular target commonly studied in life science research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P23443\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Ribosomal Protein S6 Kinase Beta-1 (RPS6KB1) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Ribosomal Protein S6 Kinase Beta-1 (RPS6KB1) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eRibosomal Protein S6 Kinase Beta-1 (RPS6KB1) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Ribosomal Protein S6 Kinase Beta-1 (RPS6KB1) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eRibosomal Protein S6 Kinase Beta-1 (RPS6KB1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003e70 kDa ribosomal protein S6 kinase 1\u003c\/strong\u003e, \u003cstrong\u003ep70 ribosomal S6 kinase alpha\u003c\/strong\u003e, and \u003cstrong\u003ep70 S6 kinase alpha\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952507810157,"sku":"E3712Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E3712Hu.jpg?v=1769146466"},{"product_id":"human-rac-alpha-serine-threonine-protein-kinase-akt1-elisa-kit-bhe12105286","title":"Human Rac-alpha Serine, Threonine-protein Kinase, AKT1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eRac-alpha Serine, Threonine-protein Kinase (AKT1)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P31749\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Rac-alpha Serine, Threonine-protein Kinase (AKT1) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Rac-alpha Serine, Threonine-protein Kinase (AKT1) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eRac-alpha Serine, Threonine-protein Kinase (AKT1) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Rac-alpha Serine, Threonine-protein Kinase (AKT1) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eRac-alpha Serine, Threonine-protein Kinase (AKT1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eAKT 1\u003c\/strong\u003e, \u003cstrong\u003eAKT1\u003c\/strong\u003e, and \u003cstrong\u003ePKB\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952509645165,"sku":"E3841Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E3841Hu.jpg?v=1769146482"},{"product_id":"human-rac-beta-serine-threonine-protein-kinase-akt2-elisa-kit-bhe12105304","title":"Human Rac-beta Serine, Threonine-protein Kinase, AKT2 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eRac-beta Serine, Threonine-protein Kinase (AKT2)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P31751\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Rac-beta Serine, Threonine-protein Kinase (AKT2) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Rac-beta Serine, Threonine-protein Kinase (AKT2) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eRac-beta Serine, Threonine-protein Kinase (AKT2) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Rac-beta Serine, Threonine-protein Kinase (AKT2) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eRac-beta Serine, Threonine-protein Kinase (AKT2)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eAKT 2\u003c\/strong\u003e, \u003cstrong\u003eAKT2\u003c\/strong\u003e, and \u003cstrong\u003ePKB beta\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952510038381,"sku":"E3864Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E3864Hu.jpg?v=1769146485"},{"product_id":"human-cyclin-dependent-kinase-20-ccrk-elisa-kit-bhe12105332","title":"Human Cyclin-dependent Kinase 20, CCRK ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase 20 (CDK20)\u003c\/strong\u003e is a molecular target commonly studied in life science research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q8IZL9\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Cyclin-dependent Kinase 20 (CDK20) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Cyclin-dependent Kinase 20 (CDK20) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eCyclin-dependent Kinase 20 (CDK20) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Cyclin-dependent Kinase 20 (CDK20) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase 20 (CDK20)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCAK-kinase p42\u003c\/strong\u003e, \u003cstrong\u003eCDK 20\u003c\/strong\u003e, and \u003cstrong\u003eCDK20\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952511807853,"sku":"E3894Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E3894Hu.jpg?v=1769146488"},{"product_id":"human-serine-threonine-protein-kinase-b-raf-braf-elisa-kit-bhe12105344","title":"Human Serine Threonine-protein Kinase B-raf, BRAF ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eSerine Threonine-protein Kinase B-raf (BRAF)\u003c\/strong\u003e is a molecular target commonly studied in cell biology research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P15056\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Serine Threonine-protein Kinase B-raf (BRAF) is frequently examined in relation to signal transduction pathways, cell cycle and stress-response programs, and organelle and membrane dynamics. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Serine Threonine-protein Kinase B-raf (BRAF) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eSerine Threonine-protein Kinase B-raf (BRAF) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Serine Threonine-protein Kinase B-raf (BRAF) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eSerine Threonine-protein Kinase B-raf (BRAF)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eBRAF\u003c\/strong\u003e, \u003cstrong\u003eB-raf\u003c\/strong\u003e, and \u003cstrong\u003eBRAF1\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952512692589,"sku":"E3906Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E3906Hu.jpg?v=1769146490"},{"product_id":"human-cyclin-dependent-kinase-9-cdk9-elisa-kit-bhe12105739","title":"Human Cyclin Dependent Kinase 9, CDK9 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin Dependent Kinase 9 (CDK9)\u003c\/strong\u003e is a molecular target commonly studied in cell biology, microbiology, and epigenetics and nuclear signaling research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P50750\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Cyclin Dependent Kinase 9 (CDK9) is frequently examined in relation to signal transduction pathways, cell cycle and stress-response programs, and organelle and membrane dynamics. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Cyclin Dependent Kinase 9 (CDK9) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eCyclin Dependent Kinase 9 (CDK9) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Cyclin Dependent Kinase 9 (CDK9) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin Dependent Kinase 9 (CDK9)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eC-2K\u003c\/strong\u003e, \u003cstrong\u003eCDK 9\u003c\/strong\u003e, and \u003cstrong\u003eCDK9\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952527733101,"sku":"E4386hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E4386hu.jpg?v=1769146536"},{"product_id":"human-low-density-lipoprotein-receptor-related-protein-5-lrp5-elisa-kit-bhe12105989","title":"Human Low Density Lipoprotein Receptor Related Protein 5, LRP5 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eLow Density Lipoprotein Receptor Related Protein 5 (LRP5)\u003c\/strong\u003e is a molecular target commonly studied in life science research. Receptors mediate cellular responses to ligands and translate extracellular cues into intracellular signaling programs.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: O75197\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Low Density Lipoprotein Receptor Related Protein 5 (LRP5) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Low Density Lipoprotein Receptor Related Protein 5 (LRP5) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eLow Density Lipoprotein Receptor Related Protein 5 (LRP5) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Low Density Lipoprotein Receptor Related Protein 5 (LRP5) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eLow Density Lipoprotein Receptor Related Protein 5 (LRP5)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eLow-density lipoprotein receptor-related protein 5\u003c\/strong\u003e, \u003cstrong\u003eLow-density lipoprotein receptor-related protein 7\u003c\/strong\u003e, and \u003cstrong\u003eLRP 5\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952535007597,"sku":"E4697Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E4697Hu.jpg?v=1769146564"},{"product_id":"human-cyclin-dependent-kinase-4-inhibitor-b-cdkn2b-elisa-kit-bhe12106503","title":"Human Cyclin-dependent Kinase 4 Inhibitor B, CDKN2B ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase 4 Inhibitor B (CDKN2B)\u003c\/strong\u003e is a molecular target commonly studied in life science research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P42772\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Cyclin-dependent Kinase 4 Inhibitor B (CDKN2B) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Cyclin-dependent Kinase 4 Inhibitor B (CDKN2B) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eCyclin-dependent Kinase 4 Inhibitor B (CDKN2B) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Cyclin-dependent Kinase 4 Inhibitor B (CDKN2B) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase 4 Inhibitor B (CDKN2B)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCDKN2B\u003c\/strong\u003e, \u003cstrong\u003eCyclin-dependent kinase 4 inhibitor B\u003c\/strong\u003e, and \u003cstrong\u003eMTS-2\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952554078573,"sku":"E5140Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E5140Hu.jpg?v=1769146650"},{"product_id":"human-cyclin-dependent-kinase-inhibitor-2a-isoforms-1-elisa-kit-bhe12106504","title":"Human Cyclin-dependent Kinase Inhibitor 2A, ISOFORMS 1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase Inhibitor 2A, ISOFORMS 1 (CDKN2A)\u003c\/strong\u003e is a molecular target commonly studied in cell biology research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P42771\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Cyclin-dependent Kinase Inhibitor 2A, ISOFORMS 1 (CDKN2A) is frequently examined in relation to signal transduction pathways, cell cycle and stress-response programs, and organelle and membrane dynamics. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Cyclin-dependent Kinase Inhibitor 2A, ISOFORMS 1 (CDKN2A) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eCyclin-dependent Kinase Inhibitor 2A, ISOFORMS 1 (CDKN2A) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Cyclin-dependent Kinase Inhibitor 2A, ISOFORMS 1 (CDKN2A) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase Inhibitor 2A, ISOFORMS 1 (CDKN2A)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eARF\u003c\/strong\u003e, \u003cstrong\u003eCDK4I\u003c\/strong\u003e, and \u003cstrong\u003eCDKN2\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952554111341,"sku":"E5141Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E5141Hu.jpg?v=1769146651"},{"product_id":"human-e3-ubiquitin-protein-ligase-mdm2-mdm2-elisa-kit-bhe12106576","title":"Human E3 Ubiquitin-protein Ligase Mdm2, MDM2 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eE3 Ubiquitin-protein Ligase Mdm2 (MDM2)\u003c\/strong\u003e is a molecular target commonly studied in cell biology research. Immunoglobulins are antibody proteins central to humoral immunity and antigen recognition.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q00987\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, E3 Ubiquitin-protein Ligase Mdm2 (MDM2) is frequently examined in relation to signal transduction pathways, cell cycle and stress-response programs, and organelle and membrane dynamics. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of E3 Ubiquitin-protein Ligase Mdm2 (MDM2) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eE3 Ubiquitin-protein Ligase Mdm2 (MDM2) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of E3 Ubiquitin-protein Ligase Mdm2 (MDM2) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eE3 Ubiquitin-protein Ligase Mdm2 (MDM2)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eACTFS\u003c\/strong\u003e, \u003cstrong\u003eDouble minute 2 protein\u003c\/strong\u003e, and \u003cstrong\u003eE3 ubiquitin-protein ligase Mdm2\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952558961005,"sku":"E5213Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E5213Hu.jpg?v=1769146674"},{"product_id":"human-eukaryotic-translation-initiation-factor-4e-binding-protein-1-eif4ebp1-elisa-kit-bhe12106631","title":"Human Eukaryotic Translation Initiation Factor 4E-binding Protein 1, EIF4EBP1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eEukaryotic Translation Initiation Factor 4E-binding Protein 1 (EIF4EBP1)\u003c\/strong\u003e is a molecular target commonly studied in epigenetics and nuclear signaling research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q13541\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Eukaryotic Translation Initiation Factor 4E-binding Protein 1 (EIF4EBP1) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Eukaryotic Translation Initiation Factor 4E-binding Protein 1 (EIF4EBP1) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eEukaryotic Translation Initiation Factor 4E-binding Protein 1 (EIF4EBP1) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Eukaryotic Translation Initiation Factor 4E-binding Protein 1 (EIF4EBP1) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eEukaryotic Translation Initiation Factor 4E-binding Protein 1 (EIF4EBP1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003e4EBP1\u003c\/strong\u003e, \u003cstrong\u003e4E-BP1\u003c\/strong\u003e, and \u003cstrong\u003eBP-1\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952563220845,"sku":"E5268Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E5268Hu.jpg?v=1769146693"},{"product_id":"human-g1-s-specific-cyclin-e1-ccne1-elisa-kit-bhe12106676","title":"Human G1 S-specific Cyclin-E1, CCNE1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eG1 S-specific Cyclin-E1 (CCNE1)\u003c\/strong\u003e is a molecular target commonly studied in cell biology research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P24864\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, G1 S-specific Cyclin-E1 (CCNE1) is frequently examined in relation to signal transduction pathways, cell cycle and stress-response programs, and organelle and membrane dynamics. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of G1 S-specific Cyclin-E1 (CCNE1) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eG1 S-specific Cyclin-E1 (CCNE1) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of G1 S-specific Cyclin-E1 (CCNE1) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eG1 S-specific Cyclin-E1 (CCNE1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCCNE\u003c\/strong\u003e, \u003cstrong\u003eCCNE1\u003c\/strong\u003e, and \u003cstrong\u003eG1\/S-specific cyclin-E1\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952568529261,"sku":"E5313Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E5313Hu.jpg?v=1769146707"},{"product_id":"human-phosphatidylinositol-3-kinase-regulatory-subunit-bbeta-pik3r2-elisa-kit-bhe12107227","title":"Human Phosphatidylinositol 3-kinase Regulatory Subunit Bbeta, PIK3R2 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ePhosphatidylinositol 3-kinase Regulatory Subunit Bbeta (PIK3R2)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction and immunology research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: O00459\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Phosphatidylinositol 3-kinase Regulatory Subunit Bbeta (PIK3R2) is frequently examined in relation to innate and adaptive immune responses, cytokine signaling networks, and immune cell activation and trafficking. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Phosphatidylinositol 3-kinase Regulatory Subunit Bbeta (PIK3R2) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003ePhosphatidylinositol 3-kinase Regulatory Subunit Bbeta (PIK3R2) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Phosphatidylinositol 3-kinase Regulatory Subunit Bbeta (PIK3R2) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ePhosphatidylinositol 3-kinase Regulatory Subunit Bbeta (PIK3R2)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eMPPH\u003c\/strong\u003e, \u003cstrong\u003eMPPH1\u003c\/strong\u003e, and \u003cstrong\u003ep85\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952592449901,"sku":"E5865Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E5865Hu.jpg?v=1769146859"},{"product_id":"human-protein-wnt-16-wnt16-elisa-kit-bhe12107370","title":"Human Protein Wnt-16, WNT16 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProtein Wnt-16 (WNT16)\u003c\/strong\u003e is a molecular target commonly studied in stem cells research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q9UBV4\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Protein Wnt-16 (WNT16) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Protein Wnt-16 (WNT16) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eProtein Wnt-16 (WNT16) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Protein Wnt-16 (WNT16) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProtein Wnt-16 (WNT16)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eProtein Wnt-16\u003c\/strong\u003e, \u003cstrong\u003eWNT 16\u003c\/strong\u003e, and \u003cstrong\u003eWNT16\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952597463405,"sku":"E6008Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E6008Hu.jpg?v=1769146882"},{"product_id":"human-proto-oncogene-wnt-1-wnt1-elisa-kit-bhe12107396","title":"Human Proto-oncogene Wnt-1, WNT1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProto-oncogene Wnt-1 (WNT1)\u003c\/strong\u003e is a molecular target commonly studied in stem cells research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P04628\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Proto-oncogene Wnt-1 (WNT1) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Proto-oncogene Wnt-1 (WNT1) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eProto-oncogene Wnt-1 (WNT1) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Proto-oncogene Wnt-1 (WNT1) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProto-oncogene Wnt-1 (WNT1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eProto-oncogene Int-1 homolog\u003c\/strong\u003e, \u003cstrong\u003eProto-oncogene Wnt-1\u003c\/strong\u003e, and \u003cstrong\u003eWNT 1\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952598118765,"sku":"E6034Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E6034Hu.jpg?v=1769146890"},{"product_id":"human-proto-oncogene-wnt-3-wnt3-elisa-kit-bhe12107397","title":"Human Proto-oncogene Wnt-3, WNT3 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProto-oncogene Wnt-3 (WNT3)\u003c\/strong\u003e is a molecular target commonly studied in neuroscience research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P56703\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Proto-oncogene Wnt-3 (WNT3) is frequently examined in relation to neuronal signaling and synaptic function, neuroinflammation and glial responses, and neurodegeneration models. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Proto-oncogene Wnt-3 (WNT3) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eProto-oncogene Wnt-3 (WNT3) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Proto-oncogene Wnt-3 (WNT3) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProto-oncogene Wnt-3 (WNT3)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eINT4\u003c\/strong\u003e, \u003cstrong\u003eProto-oncogene Int-4 homolog\u003c\/strong\u003e, and \u003cstrong\u003eProto-oncogene Wnt-3\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952598151533,"sku":"E6035Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E6035Hu.jpg?v=1769146890"},{"product_id":"human-gtpase-kras-kras-elisa-kit-bhe12107810","title":"Human Gtpase Kras, KRAS ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eGtpase Kras (KRAS)\u003c\/strong\u003e is a molecular target commonly studied in life science research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P01116\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Gtpase Kras (KRAS) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Gtpase Kras (KRAS) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eGtpase Kras (KRAS) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Gtpase Kras (KRAS) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eGtpase Kras (KRAS)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCFC2\u003c\/strong\u003e, \u003cstrong\u003ec-Ki-ras\u003c\/strong\u003e, and \u003cstrong\u003ec-Ki-ras2\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952609620333,"sku":"E6448Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E6448Hu.jpg?v=1769146970"},{"product_id":"mouse-adenomatosis-polyposis-coli-protein-apc-elisa-kit-bhe12108695","title":"Mouse Adenomatosis Polyposis Coli Protein, APC ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eAdenomatosis Polyposis Coli Protein (APC)\u003c\/strong\u003e is a molecular target commonly studied in cell biology, neuroscience, and epigenetics and nuclear signaling research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q61315\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Adenomatosis Polyposis Coli Protein (APC) is frequently examined in relation to signal transduction pathways, cell cycle and stress-response programs, and organelle and membrane dynamics. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Adenomatosis Polyposis Coli Protein (APC) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eAdenomatosis Polyposis Coli Protein (APC) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Adenomatosis Polyposis Coli Protein (APC) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eAdenomatosis Polyposis Coli Protein (APC)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eAdenomatous polyposis coli protein\u003c\/strong\u003e, \u003cstrong\u003eAI047805\u003c\/strong\u003e, and \u003cstrong\u003eAPC\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952615944557,"sku":"E0822Mo-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0822Mo.jpg?v=1769147021"},{"product_id":"mouse-cyclin-dependent-kinase-4-cdk-4-elisa-kit-bhe12108836","title":"Mouse Cyclin-dependent Kinase 4, CDK-4 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase 4 (CDK4)\u003c\/strong\u003e is a molecular target commonly studied in cell biology research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P30285\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Cyclin-dependent Kinase 4 (CDK4) is frequently examined in relation to signal transduction pathways, cell cycle and stress-response programs, and organelle and membrane dynamics. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Cyclin-dependent Kinase 4 (CDK4) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eCyclin-dependent Kinase 4 (CDK4) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Cyclin-dependent Kinase 4 (CDK4) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCyclin-dependent Kinase 4 (CDK4)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCDK 4\u003c\/strong\u003e, \u003cstrong\u003eCDK4\u003c\/strong\u003e, and \u003cstrong\u003eCell division protein kinase 4\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952617025901,"sku":"E0965Mo-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0965Mo.jpg?v=1769147029"},{"product_id":"mouse-glycogen-synthase-kinase-3-alpha-gsk3a-elisa-kit-bhe12109115","title":"Mouse Glycogen Synthase Kinase-3 Alpha, GSK3A ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eGlycogen Synthase Kinase-3 Alpha (GSK3A)\u003c\/strong\u003e is a molecular target commonly studied in life science research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q2NL51\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Glycogen Synthase Kinase-3 Alpha (GSK3A) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Glycogen Synthase Kinase-3 Alpha (GSK3A) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eGlycogen Synthase Kinase-3 Alpha (GSK3A) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Glycogen Synthase Kinase-3 Alpha (GSK3A) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eGlycogen Synthase Kinase-3 Alpha (GSK3A)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eGlycogen Synthase kinase-3 alpha\u003c\/strong\u003e, \u003cstrong\u003eGSK 3A\u003c\/strong\u003e, and \u003cstrong\u003eGSK-3 alpha\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952620204397,"sku":"E1250Mo-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E1250Mo.jpg?v=1769147058"},{"product_id":"mouse-glycogen-synthase-kinase-3-beta-gsk3b-elisa-kit-bhe12109116","title":"Mouse Glycogen Synthase Kinase-3 Beta, GSK3B ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eGlycogen Synthase Kinase-3 Beta (GSK3B)\u003c\/strong\u003e is a molecular target commonly studied in neuroscience research. Enzymes influence signaling and metabolism through catalytic activity that can vary across tissues and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q9WV60\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Glycogen Synthase Kinase-3 Beta (GSK3B) is frequently examined in relation to neuronal signaling and synaptic function, neuroinflammation and glial responses, and neurodegeneration models. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Glycogen Synthase Kinase-3 Beta (GSK3B) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eGlycogen Synthase Kinase-3 Beta (GSK3B) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Glycogen Synthase Kinase-3 Beta (GSK3B) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eGlycogen Synthase Kinase-3 Beta (GSK3B)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eGlycogen Synthase kinase-3 beta\u003c\/strong\u003e, \u003cstrong\u003eGSK 3B\u003c\/strong\u003e, and \u003cstrong\u003eGSK-3 beta\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952620237165,"sku":"E1251Mo-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E1251Mo.jpg?v=1769147059"},{"product_id":"mouse-protein-wnt-4-wnt4elisa-kit-bhe12109349","title":"Mouse Protein Wnt-4, WNT4ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProtein Wnt-4, WNT4ELISA Kit (WNT4)\u003c\/strong\u003e is a molecular target commonly studied in stem cells research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P22724\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Protein Wnt-4, WNT4ELISA Kit (WNT4) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Protein Wnt-4, WNT4ELISA Kit (WNT4) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eProtein Wnt-4, WNT4ELISA Kit (WNT4) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Protein Wnt-4, WNT4ELISA Kit (WNT4) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProtein Wnt-4, WNT4ELISA Kit (WNT4)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eProtein Wnt-4\u003c\/strong\u003e, \u003cstrong\u003eWNT 4\u003c\/strong\u003e, and \u003cstrong\u003eWNT4\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952624464237,"sku":"E1495Mo-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E1495Mo.jpg?v=1769147078"},{"product_id":"mouse-proto-oncogene-wnt-1-wnt1-elisa-kit-bhe12109413","title":"Mouse Proto-oncogene Wnt-1, WNT1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProto-oncogene Wnt-1 (WNT1)\u003c\/strong\u003e is a molecular target commonly studied in stem cells research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P04426\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Proto-oncogene Wnt-1 (WNT1) is frequently examined in relation to mechanistic biology studies, biomarker-focused profiling, and disease-model research. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Proto-oncogene Wnt-1 (WNT1) can vary across tissues and cell types and may change under conditions such as immune activation, stress responses, injury, infection, or metabolic perturbation. Reported regulation may involve transcriptional control as well as post-translational processes that influence stability, localization, processing, or secretion.\u003c\/p\u003e\u003ch2\u003eResearch and disease relevance\u003c\/h2\u003e\u003cp\u003eProto-oncogene Wnt-1 (WNT1) has been reported as a useful readout in studies of physiological regulation and disease-associated processes. These observations make it relevant for hypothesis-driven research and biomarker exploration, while interpretation should remain grounded in the specific species, sample matrix, and study design.\u003c\/p\u003e\u003ch2\u003eInterpreting concentration measurements\u003c\/h2\u003e\u003cp\u003eMeasured levels of Proto-oncogene Wnt-1 (WNT1) can reflect multiple biological factors, including production rate, turnover, compartmental distribution, and sample composition. As a result, conclusions are often supported by considering broader pathway context and complementary readouts rather than relying on a single analyte alone.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProto-oncogene Wnt-1 (WNT1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eInt\u003c\/strong\u003e, \u003cstrong\u003eInt-1\u003c\/strong\u003e, and \u003cstrong\u003eProto-oncogene Int-1\u003c\/strong\u003e in publications and databases. Nomenclature differences and species context can influence how results are compared across studies.\u003c\/p\u003e","brand":"Bioassay Technology Laboratory","offers":[{"title":"96T","offer_id":52952625840493,"sku":"E1566Mo-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E1566Mo.jpg?v=1769147088"}],"url":"https:\/\/www.ebiohippo.com\/collections\/rtc-cancer-oncology-signaling-elisa-kits.oembed?page=17","provider":"BioHippo","version":"1.0","type":"link"}