{"title":"Prolactin \/ hCG Markers","description":null,"products":[{"product_id":"mouse-prolactin-elisa-kit-ez-set-diy-antibody-pairs-bhe21000008","title":"Mouse Prolactin ELISA Kit EZ-Set™ (DIY Antibody Pairs)","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eAlso known as:\u003c\/strong\u003e Prolactin, PRL.\u003c\/p\u003e\u003cp\u003eMouse \u003cstrong\u003eProlactin\u003c\/strong\u003e (\u003cstrong\u003ePrl\u003c\/strong\u003e) is widely studied as a molecular readout in experimental models where changes in protein abundance reflect underlying biology. This target is frequently investigated in \u003cstrong\u003eOncology \u0026amp; Angiogenesis\u003c\/strong\u003e research contexts. This analyte is often discussed in the context of \u003cstrong\u003eendocrine signaling and metabolic homeostasis\u003c\/strong\u003e. Hormonal and adipokine signaling coordinates systemic energy balance, appetite, glucose handling, and tissue-specific metabolic programs.\u003c\/p\u003e\u003ch2\u003eBiological context\u003c\/h2\u003e\u003cp\u003eIn experimental systems, protein abundance can reflect regulated expression, secretion, processing, or clearance. Interpreting changes benefits from considering compartment (cell-associated vs soluble), the time scale of regulation, and whether complexes or modified forms contribute to the measured signal.\u003c\/p\u003e\u003ch2\u003eWhy it matters in research\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eSystems-level readout:\u003c\/strong\u003e Quantification supports comparisons across conditions, time points, and treatment groups.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eMechanistic interpretation:\u003c\/strong\u003e Pairing with upstream regulators and downstream markers helps contextualize changes.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eBiomarker-style profiling:\u003c\/strong\u003e Measuring panels of related analytes can improve interpretability in complex models.\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Boster Bio","offers":[{"title":"5 plates\/kit","offer_id":52920801460589,"sku":"EZ0594","price":500.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/ez0594-2-ELISA-mouse-prolactin-ez-set-elisa-kit-diy-antibody-pairs.jpg?v=1769077470"},{"product_id":"human-prolactin-elisa-kit-picokine-bhe21000538","title":"Human Prolactin ELISA Kit PicoKine®","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eAlso known as:\u003c\/strong\u003e Prolactin, PRL.\u003c\/p\u003e\u003cp\u003eHuman \u003cstrong\u003eProlactin\u003c\/strong\u003e (\u003cstrong\u003ePRL\u003c\/strong\u003e) is an established target in many assay panels, supporting hypothesis testing across diverse biological systems. This target is frequently investigated in \u003cstrong\u003eCoagulation \u0026amp; Hemostasis\u003c\/strong\u003e research contexts. This analyte is often discussed in the context of \u003cstrong\u003eendocrine signaling and metabolic homeostasis\u003c\/strong\u003e. Hormonal and adipokine signaling coordinates systemic energy balance, appetite, glucose handling, and tissue-specific metabolic programs.\u003c\/p\u003e\u003ch2\u003eBiological context\u003c\/h2\u003e\u003cp\u003eIn experimental systems, protein abundance can reflect regulated expression, secretion, processing, or clearance. Interpreting changes benefits from considering compartment (cell-associated vs soluble), the time scale of regulation, and whether complexes or modified forms contribute to the measured signal.\u003c\/p\u003e\u003ch2\u003eWhy it matters in research\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eSystems-level readout:\u003c\/strong\u003e Quantification supports comparisons across conditions, time points, and treatment groups.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eMechanistic interpretation:\u003c\/strong\u003e Pairing with upstream regulators and downstream markers helps contextualize changes.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eBiomarker-style profiling:\u003c\/strong\u003e Measuring panels of related analytes can improve interpretability in complex models.\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Boster Bio","offers":[{"title":"96 wells\/kit, with removable strips.","offer_id":52920819712365,"sku":"EK0593","price":499.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/ek0593.png?v=1769077732"},{"product_id":"mouse-prolactin-elisa-kit-picokine-bhe21000539","title":"Mouse Prolactin ELISA Kit PicoKine®","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eAlso known as:\u003c\/strong\u003e Prolactin, PRL.\u003c\/p\u003e\u003cp\u003eMouse \u003cstrong\u003eProlactin\u003c\/strong\u003e (\u003cstrong\u003ePRL\u003c\/strong\u003e) is an established target in many assay panels, supporting hypothesis testing across diverse biological systems. This target is frequently investigated in \u003cstrong\u003eMolecular \u0026amp; Cellular Biology\u003c\/strong\u003e research contexts. This analyte is often discussed in the context of \u003cstrong\u003eendocrine signaling and metabolic homeostasis\u003c\/strong\u003e. Hormonal and adipokine signaling coordinates systemic energy balance, appetite, glucose handling, and tissue-specific metabolic programs.\u003c\/p\u003e\u003ch2\u003eBiological context\u003c\/h2\u003e\u003cp\u003eIn experimental systems, protein abundance can reflect regulated expression, secretion, processing, or clearance. Interpreting changes benefits from considering compartment (cell-associated vs soluble), the time scale of regulation, and whether complexes or modified forms contribute to the measured signal.\u003c\/p\u003e\u003ch2\u003eWhy it matters in research\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eSystems-level readout:\u003c\/strong\u003e Quantification supports comparisons across conditions, time points, and treatment groups.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eMechanistic interpretation:\u003c\/strong\u003e Pairing with upstream regulators and downstream markers helps contextualize changes.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eBiomarker-style profiling:\u003c\/strong\u003e Measuring panels of related analytes can improve interpretability in complex models.\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Boster Bio","offers":[{"title":"96 wells\/kit, with removable strips.","offer_id":52920819745133,"sku":"EK0594","price":499.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/ek0594.png?v=1769077732"},{"product_id":"goat-prolactin-prl-elisa-kit-bhe12101364","title":"Goat Prolactin, PRL ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProlactin (PRL)\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: Q28318\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Prolactin (PRL) 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 Prolactin (PRL) 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\u003eProlactin (PRL) 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 Prolactin (PRL) 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\u003eProlactin (PRL)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003ePRL\u003c\/strong\u003e and \u003cstrong\u003eProlactin\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":52952453349741,"sku":"E0039GO-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0039GO.jpg?v=1769145988"},{"product_id":"human-prolactin-receptor-prlr-elisa-kit-bhe12105916","title":"Human Prolactin Receptor, PRLR ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProlactin Receptor (PRLR)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction 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: P16471\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Prolactin Receptor (PRLR) 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 Prolactin Receptor (PRLR) 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\u003eProlactin Receptor (PRLR) 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 Prolactin Receptor (PRLR) 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\u003eProlactin Receptor (PRLR)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003ePRLR\u003c\/strong\u003e, \u003cstrong\u003ePRL-R\u003c\/strong\u003e, and \u003cstrong\u003eProlactin receptor\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":52952532058477,"sku":"E4610Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E4610Hu.jpg?v=1769146552"},{"product_id":"mouse-prolactin-receptor-prlr-elisa-kit-bhe12110177","title":"Mouse Prolactin Receptor, PRLR ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProlactin Receptor (PRLR)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction 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: Q08501\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Prolactin Receptor (PRLR) 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 Prolactin Receptor (PRLR) 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\u003eProlactin Receptor (PRLR) 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 Prolactin Receptor (PRLR) 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\u003eProlactin Receptor (PRLR)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eAI987712\u003c\/strong\u003e, \u003cstrong\u003ePr\u003c\/strong\u003e, and \u003cstrong\u003ePr-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":52952651039085,"sku":"E2366Mo-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2366Mo.jpg?v=1769147237"},{"product_id":"porcine-prolactin-prl-elisa-kit-bhe12110609","title":"Porcine Prolactin, PRL ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProlactin (PRL)\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: P01238\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Prolactin (PRL) 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 Prolactin (PRL) 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\u003eProlactin (PRL) 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 Prolactin (PRL) 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\u003eProlactin (PRL)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003ePRL\u003c\/strong\u003e and \u003cstrong\u003eProlactin\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":52952659886445,"sku":"E0194Po-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0194Po.jpg?v=1769147296"},{"product_id":"rat-chromogranin-a-cga-elisa-kit-bhe12111835","title":"Rat Chromogranin-A, CGA ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eChromogranin-A (CgA)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction, neuroscience, 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: P10354\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Chromogranin-A (CgA) 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 Chromogranin-A (CgA) 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\u003eChromogranin-A (CgA) 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 Chromogranin-A (CgA) 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\u003eChromogranin-A (CgA)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eBeta-granin\u003c\/strong\u003e, \u003cstrong\u003eCatestatin\u003c\/strong\u003e, and \u003cstrong\u003eCgA\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":52952673845613,"sku":"E0557Ra-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0557Ra.jpg?v=1769147378"},{"product_id":"rat-prolactin-receptor-prlr-elisa-kit-bhe12113344","title":"Rat Prolactin Receptor, PRLR ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProlactin Receptor (PRLR)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction 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: P05710\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Prolactin Receptor (PRLR) 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 Prolactin Receptor (PRLR) 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\u003eProlactin Receptor (PRLR) 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 Prolactin Receptor (PRLR) 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\u003eProlactin Receptor (PRLR)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eLactogen receptor\u003c\/strong\u003e, \u003cstrong\u003ePRLR\u003c\/strong\u003e, and \u003cstrong\u003ePRL-R\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":52952707989869,"sku":"E2212Ra-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2212Ra.jpg?v=1769147545"},{"product_id":"sheep-prolactin-prl-elisa-kit-bhe12113502","title":"Sheep Prolactin, PRL ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProlactin (PRL)\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: P01240\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Prolactin (PRL) 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 Prolactin (PRL) 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\u003eProlactin (PRL) 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 Prolactin (PRL) 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\u003eProlactin (PRL)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003ePRL\u003c\/strong\u003e and \u003cstrong\u003eProlactin\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":52952712872301,"sku":"E0022Sh-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0022Sh.jpg?v=1769147568"},{"product_id":"horse-prolactin-prl-elisa-kit-bhe10500952","title":"Horse Prolactin(PRL) ELISA kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eProlactin(PRL)\u003c\/strong\u003e is a biological molecule commonly studied in signal transduction research. 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It is commonly used as a molecular readout in mechanistic and biomarker-focused studies.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P0DN86\u003c\/p\u003e\u003ch2\u003eBiological context\u003c\/h2\u003e\u003cp\u003eResearchers often monitor Chorionic Gonadotrophin in serum, plasma, urine, and cell culture supernates to better understand themes such as tumor microenvironment biology, cell proliferation and apoptosis, and metastasis and invasion pathways. In many model systems, measured levels can shift with physiology, experimental perturbation, or disease-associated changes, making careful biological interpretation important.\u003c\/p\u003e\u003ch2\u003eInterpreting changes in measured levels\u003c\/h2\u003e\u003cp\u003eDepending on sample matrix and study design, increases or decreases in Chorionic Gonadotrophin may reflect differences in expression, secretion, turnover, or compartmentalization rather than a single mechanism. 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When integrating results with other readouts, consider species biology, sample type, and the broader pathway context that Chorionic Gonadotrophin participates in.\u003c\/p\u003e","brand":"CUSABIO TECHNOLOGY LLC","offers":[{"title":"96 T","offer_id":52959464849773,"sku":"CSB-E05060h-96T","price":458.0,"currency_code":"USD","in_stock":true},{"title":"96 T×5","offer_id":52959464882541,"sku":"CSB-E05060h-96TX5","price":1969.4,"currency_code":"USD","in_stock":true},{"title":"96 T×10","offer_id":52959464915309,"sku":"CSB-E05060h-96TX10","price":3781.2,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/CSB-E05060h.png?v=1769246849"},{"product_id":"human-glycoprotein-hormones-alpha-chain-cga-elisa-kit-bhe10502560","title":"Human Glycoprotein hormones alpha chain(CGA) ELISA kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eGlycoprotein hormones alpha chain(CGA)\u003c\/strong\u003e is a biological molecule commonly studied in cancer research. Hormones and peptide mediators support systemic communication across organs and physiological states.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P01215\u003c\/p\u003e\u003ch2\u003eBiological context\u003c\/h2\u003e\u003cp\u003eResearchers often monitor Glycoprotein hormones alpha chain(CGA) in serum, plasma, and cell culture supernates to better understand themes such as tumor microenvironment biology, cell proliferation and apoptosis, and metastasis and invasion pathways. 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Interpretation is typically strengthened by evaluating related molecules (for example, cell-cycle regulators, invasion\/ECM markers, and immune-oncology mediators) and by keeping pre-analytical variables consistent across groups.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003eIn publications and databases, Glycoprotein hormones alpha chain(CGA) may also appear under names such as \u003cstrong\u003eAnterior pituitary glycoprotein hormones common subunit alpha\u003c\/strong\u003e and \u003cstrong\u003eCG alpha\u003c\/strong\u003e. When comparing studies, confirm that the reported analyte refers to the same molecule and species context.\u003c\/p\u003e\u003ch2\u003eWhy ELISA data are widely used\u003c\/h2\u003e\u003cp\u003eELISA is a common approach for quantitative measurement of proteins and biomarkers in complex samples, enabling comparisons across experimental groups and time points. When integrating results with other readouts, consider species biology, sample type, and the broader pathway context that Glycoprotein hormones alpha chain(CGA) participates in.\u003c\/p\u003e","brand":"CUSABIO TECHNOLOGY LLC","offers":[{"title":"96 T","offer_id":52959505023341,"sku":"CSB-EL005293HU-96T","price":595.0,"currency_code":"USD","in_stock":true},{"title":"96 T×5","offer_id":52959505056109,"sku":"CSB-EL005293HU-96TX5","price":2439.5,"currency_code":"USD","in_stock":true},{"title":"96 T×10","offer_id":52959505088877,"sku":"CSB-EL005293HU-96TX10","price":4683.8,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/CSB-EL005293HU.png?v=1769246962"},{"product_id":"human-hyperglycosylated-chorionic-gonadotropin-hcg-elisa-kit-bhe10502799","title":"Human Hyperglycosylated Chorionic Gonadotropin(hCG) ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eHyperglycosylated Chorionic Gonadotropin(hCG)\u003c\/strong\u003e is a biological molecule commonly studied in cancer research. 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Interpretation is typically strengthened by evaluating related molecules (for example, cell-cycle regulators, invasion\/ECM markers, and immune-oncology mediators) and by keeping pre-analytical variables consistent across groups.\u003c\/p\u003e\u003ch2\u003eWhy ELISA data are widely used\u003c\/h2\u003e\u003cp\u003eELISA is a common approach for quantitative measurement of proteins and biomarkers in complex samples, enabling comparisons across experimental groups and time points. 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The microtiter plate provided in this kit has been pre-coated with an antibody specific to Cattle PRL. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Cattle PRL. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Cattle PRL, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Cattle PRL in the samples is then determined by comparing the OD of the samples to the standard curve.\u003c\/strong\u003e. 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The microtiter plate provided in this kit has been pre-coated with an antibody specific to Chicken PRL. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Chicken PRL. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Chicken PRL, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Chicken PRL in the samples is then determined by comparing the OD of the samples to the standard curve.\u003c\/strong\u003e. 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The microtiter plate provided in this kit has been pre-coated with an antibody specific to Mouse hCG. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse hCG. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Mouse hCG, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mouse hCG in the samples is then determined by comparing the OD of the samples to the standard curve.\u003c\/strong\u003e. 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When comparing results across studies, confirm that the reported analyte refers to the same molecule, species context, and molecular form (e.g., precursor vs mature protein, or soluble vs membrane-associated forms).\u003c\/p\u003e\u003ch2\u003eWhy it matters in research\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eUnderstanding how LHCGR relates to signal transduction, tissue homeostasis, stress responses, and disease-model biology in developmental biology and signal transduction research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in LHCGR levels alongside other pathway components or complementary markers.\u003c\/li\u003e\n\u003cli\u003eConnecting molecular changes to phenotypes such as inflammation, remodeling, metabolism shifts, or cell-state transitions (context-dependent).\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eMolecular forms and interpretation\u003c\/h2\u003e\u003cp\u003eFor some targets, isoforms, proteolytic processing, or post-translational modifications (such as phosphorylation or glycosylation) can influence function and apparent abundance. If multiple molecular forms are expected in your model, align interpretation with the form most relevant to the biological question.\u003c\/p\u003e\u003ch2\u003eDisease and translational relevance\u003c\/h2\u003e\u003cp\u003eLHCGR has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with developmental biology and signal transduction studies. These associations are interpreted as research findings rather than diagnostic or therapeutic claims, and they should be evaluated alongside model-specific covariates and study design.\u003c\/p\u003e","brand":"Fine Test","offers":[{"title":"96 T","offer_id":52974922727789,"sku":"EH1592-96T","price":520.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_9271805d-5c57-486c-8404-27a597c58cdb.jpg?v=1769597994"},{"product_id":"mouse-cga-glycoprotein-hormones-alpha-chain-elisa-kit-bhe10804330","title":"Mouse Cga (Glycoprotein hormones alpha chain) ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003emouse Cga (Glycoprotein hormones alpha chain)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction, metabolism, and cancer research. Hormones and endocrine mediators support long-range communication between organs and help maintain physiological homeostasis.\u003c\/p\u003e\u003ch2\u003eBiological role and mechanism\u003c\/h2\u003e\u003cp\u003eThe biological role of Cga is typically understood in terms of its molecular category and interaction network. Depending on the model system, it may participate in cell–cell communication, intracellular signaling, enzymatic processing, or regulation of gene expression programs. Mechanistic interpretation is often strengthened by considering upstream regulators and downstream readouts rather than relying on a single marker.\u003c\/p\u003e\u003cp\u003eExpression and abundance of Cga can vary by tissue, cell type, and physiological state. In many systems, levels are influenced by factors such as developmental stage, immune activation, metabolic status, and cellular stress. Because sample matrix and pre-analytical handling can affect measured concentrations, interpretation is typically strongest when experiments keep collection and processing consistent across groups.\u003c\/p\u003e\u003ch2\u003eNomenclature and related terms\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCga (Glycoprotein hormones alpha chain)\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eGlycoprotein hormones alpha chain\u003c\/strong\u003e, \u003cstrong\u003eAnterior pituitary glycoprotein hormones common subunit alpha\u003c\/strong\u003e, and \u003cstrong\u003eFollicle-stimulating hormone alpha chain\u003c\/strong\u003e in the literature or in databases. When comparing results across studies, confirm that the reported analyte refers to the same molecule, species context, and molecular form (e.g., precursor vs mature protein, or soluble vs membrane-associated forms).\u003c\/p\u003e\u003ch2\u003eWhy it matters in research\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eUnderstanding how Cga relates to energy homeostasis, glucose and lipid metabolism, insulin sensitivity and endocrine regulation, and adipose–liver crosstalk in signal transduction, metabolism, and cancer research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in Cga levels alongside other pathway components or complementary markers.\u003c\/li\u003e\n\u003cli\u003eConnecting molecular changes to phenotypes such as inflammation, remodeling, metabolism shifts, or cell-state transitions (context-dependent).\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eMolecular forms and interpretation\u003c\/h2\u003e\u003cp\u003eFor some targets, isoforms, proteolytic processing, or post-translational modifications (such as phosphorylation or glycosylation) can influence function and apparent abundance. If multiple molecular forms are expected in your model, align interpretation with the form most relevant to the biological question.\u003c\/p\u003e\u003ch2\u003eDisease and translational relevance\u003c\/h2\u003e\u003cp\u003eCga has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with signal transduction, metabolism, and cancer studies. These associations are interpreted as research findings rather than diagnostic or therapeutic claims, and they should be evaluated alongside model-specific covariates and study design.\u003c\/p\u003e","brand":"Fine Test","offers":[{"title":"96 T","offer_id":52974927806829,"sku":"EM0219-96T","price":520.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_497b18cf-9daf-4fe6-a0be-0b043cb4cc94.jpg?v=1769598028"},{"product_id":"rat-cga-glycoprotein-hormones-alpha-chain-elisa-kit-bhe10806533","title":"Rat Cga (Glycoprotein hormones alpha chain) ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003erat Cga (Glycoprotein hormones alpha chain)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction, metabolism, and cancer research. Hormones and endocrine mediators support long-range communication between organs and help maintain physiological homeostasis.\u003c\/p\u003e\u003ch2\u003eBiological role and mechanism\u003c\/h2\u003e\u003cp\u003eThe biological role of Cga is typically understood in terms of its molecular category and interaction network. Depending on the model system, it may participate in cell–cell communication, intracellular signaling, enzymatic processing, or regulation of gene expression programs. Mechanistic interpretation is often strengthened by considering upstream regulators and downstream readouts rather than relying on a single marker.\u003c\/p\u003e\u003cp\u003eExpression and abundance of Cga can vary by tissue, cell type, and physiological state. In many systems, levels are influenced by factors such as developmental stage, immune activation, metabolic status, and cellular stress. Because sample matrix and pre-analytical handling can affect measured concentrations, interpretation is typically strongest when experiments keep collection and processing consistent across groups.\u003c\/p\u003e\u003ch2\u003eNomenclature and related terms\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCga (Glycoprotein hormones alpha chain)\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eGlycoprotein hormones alpha chain\u003c\/strong\u003e, \u003cstrong\u003eAnterior pituitary glycoprotein hormones common subunit alpha\u003c\/strong\u003e, and \u003cstrong\u003eFollicle-stimulating hormone alpha chain\u003c\/strong\u003e in the literature or in databases. When comparing results across studies, confirm that the reported analyte refers to the same molecule, species context, and molecular form (e.g., precursor vs mature protein, or soluble vs membrane-associated forms).\u003c\/p\u003e\u003ch2\u003eWhy it matters in research\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eUnderstanding how Cga relates to energy homeostasis, glucose and lipid metabolism, insulin sensitivity and endocrine regulation, and adipose–liver crosstalk in signal transduction, metabolism, and cancer research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in Cga levels alongside other pathway components or complementary markers.\u003c\/li\u003e\n\u003cli\u003eConnecting molecular changes to phenotypes such as inflammation, remodeling, metabolism shifts, or cell-state transitions (context-dependent).\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eMolecular forms and interpretation\u003c\/h2\u003e\u003cp\u003eFor some targets, isoforms, proteolytic processing, or post-translational modifications (such as phosphorylation or glycosylation) can influence function and apparent abundance. If multiple molecular forms are expected in your model, align interpretation with the form most relevant to the biological question.\u003c\/p\u003e\u003ch2\u003eDisease and translational relevance\u003c\/h2\u003e\u003cp\u003eCga has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with signal transduction, metabolism, and cancer studies. These associations are interpreted as research findings rather than diagnostic or therapeutic claims, and they should be evaluated alongside model-specific covariates and study design.\u003c\/p\u003e","brand":"Fine Test","offers":[{"title":"96 T","offer_id":52975332393325,"sku":"ER0088-96T","price":520.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_ddaaccaa-3c29-404c-851a-9f20fab75064.jpg?v=1769598747"},{"product_id":"human-hcg-igg-human-chorionic-gonadotropin-immunoglobulin-g-elisa-kit-bhe10807299","title":"Human HCG-IgG (Human chorionic gonadotropin-Immunoglobulin G) ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ehuman HCG-IgG (Human chorionic gonadotropin-Immunoglobulin G)\u003c\/strong\u003e is a molecular target commonly studied in biomedical research. Circulating plasma proteins support transport, buffering, and homeostatic processes in blood and extracellular fluids.\u003c\/p\u003e\u003ch2\u003eBiological role and mechanism\u003c\/h2\u003e\u003cp\u003eThe biological role of HCG-IgG is typically understood in terms of its molecular category and interaction network. Depending on the model system, it may participate in cell–cell communication, intracellular signaling, enzymatic processing, or regulation of gene expression programs. Mechanistic interpretation is often strengthened by considering upstream regulators and downstream readouts rather than relying on a single marker.\u003c\/p\u003e\u003cp\u003eExpression and abundance of HCG-IgG can vary by tissue, cell type, and physiological state. In many systems, levels are influenced by factors such as developmental stage, immune activation, metabolic status, and cellular stress. Because sample matrix and pre-analytical handling can affect measured concentrations, interpretation is typically strongest when experiments keep collection and processing consistent across groups.\u003c\/p\u003e\u003ch2\u003eNomenclature and related terms\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eHCG-IgG (Human chorionic gonadotropin-Immunoglobulin G)\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eHCG IgG\u003c\/strong\u003e and \u003cstrong\u003eHuman chorionic gonadotropin-Immunoglobulin G\u003c\/strong\u003e in the literature or in databases. When comparing results across studies, confirm that the reported analyte refers to the same molecule, species context, and molecular form (e.g., precursor vs mature protein, or soluble vs membrane-associated forms).\u003c\/p\u003e\u003ch2\u003eWhy it matters in research\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eUnderstanding how HCG-IgG relates to signal transduction, tissue homeostasis, stress responses, and disease-model biology in biomedical research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in HCG-IgG levels alongside other pathway components or complementary markers.\u003c\/li\u003e\n\u003cli\u003eConnecting molecular changes to phenotypes such as inflammation, remodeling, metabolism shifts, or cell-state transitions (context-dependent).\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eMolecular forms and interpretation\u003c\/h2\u003e\u003cp\u003eFor some targets, isoforms, proteolytic processing, or post-translational modifications (such as phosphorylation or glycosylation) can influence function and apparent abundance. If multiple molecular forms are expected in your model, align interpretation with the form most relevant to the biological question.\u003c\/p\u003e\u003ch2\u003eDisease and translational relevance\u003c\/h2\u003e\u003cp\u003eHCG-IgG has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with biomedical studies. These associations are interpreted as research findings rather than diagnostic or therapeutic claims, and they should be evaluated alongside model-specific covariates and study design.\u003c\/p\u003e","brand":"Fine Test","offers":[{"title":"96 T","offer_id":52975401369965,"sku":"EH4419-96T","price":455.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_69065502-22dc-400e-9f24-253dd5fd6303.jpg?v=1769599026"},{"product_id":"human-hcg-igm-human-chorionic-gonadotropin-immunoglobulin-m-elisa-kit-bhe10810011","title":"Human HCG-IgM (Human chorionic gonadotropin-Immunoglobulin M) ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ehuman HCG-IgM (Human chorionic gonadotropin-Immunoglobulin M)\u003c\/strong\u003e is a molecular target commonly studied in biomedical research. Circulating plasma proteins support transport, buffering, and homeostatic processes in blood and extracellular fluids.\u003c\/p\u003e\u003ch2\u003eBiological role and mechanism\u003c\/h2\u003e\u003cp\u003eThe biological role of HCG-IgM is typically understood in terms of its molecular category and interaction network. Depending on the model system, it may participate in cell–cell communication, intracellular signaling, enzymatic processing, or regulation of gene expression programs. Mechanistic interpretation is often strengthened by considering upstream regulators and downstream readouts rather than relying on a single marker.\u003c\/p\u003e\u003cp\u003eExpression and abundance of HCG-IgM can vary by tissue, cell type, and physiological state. In many systems, levels are influenced by factors such as developmental stage, immune activation, metabolic status, and cellular stress. Because sample matrix and pre-analytical handling can affect measured concentrations, interpretation is typically strongest when experiments keep collection and processing consistent across groups.\u003c\/p\u003e\u003ch2\u003eNomenclature and related terms\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eHCG-IgM (Human chorionic gonadotropin-Immunoglobulin M)\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eHCG-IgM\u003c\/strong\u003e and \u003cstrong\u003eHuman chorionic gonadotropin-Immunoglobulin M\u003c\/strong\u003e in the literature or in databases. When comparing results across studies, confirm that the reported analyte refers to the same molecule, species context, and molecular form (e.g., precursor vs mature protein, or soluble vs membrane-associated forms).\u003c\/p\u003e\u003ch2\u003eWhy it matters in research\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eUnderstanding how HCG-IgM relates to signal transduction, tissue homeostasis, stress responses, and disease-model biology in biomedical research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in HCG-IgM levels alongside other pathway components or complementary markers.\u003c\/li\u003e\n\u003cli\u003eConnecting molecular changes to phenotypes such as inflammation, remodeling, metabolism shifts, or cell-state transitions (context-dependent).\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eMolecular forms and interpretation\u003c\/h2\u003e\u003cp\u003eFor some targets, isoforms, proteolytic processing, or post-translational modifications (such as phosphorylation or glycosylation) can influence function and apparent abundance. If multiple molecular forms are expected in your model, align interpretation with the form most relevant to the biological question.\u003c\/p\u003e\u003ch2\u003eDisease and translational relevance\u003c\/h2\u003e\u003cp\u003eHCG-IgM has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with biomedical studies. These associations are interpreted as research findings rather than diagnostic or therapeutic claims, and they should be evaluated alongside model-specific covariates and study design.\u003c\/p\u003e","brand":"Fine Test","offers":[{"title":"96 T","offer_id":52975487025517,"sku":"EH4768-96T","price":455.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_fc01da1a-e007-4fb4-9e98-bfdaffbcf8ae.jpg?v=1769599884"},{"product_id":"mouse-cga-glycoprotein-hormones-alpha-chain-quicktest-elisa-kit-bhe10810351","title":"Mouse Cga (Glycoprotein hormones alpha chain) QuickTest ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003emouse Cga (Glycoprotein hormones alpha chain) QuickTest\u003c\/strong\u003e is a molecular target commonly studied in biomedical research. Hormones and endocrine mediators support long-range communication between organs and help maintain physiological homeostasis.\u003c\/p\u003e\u003ch2\u003eBiological role and mechanism\u003c\/h2\u003e\u003cp\u003eThe biological role of Cga (Glycoprotein hormones alpha chain) QuickTest is typically understood in terms of its molecular category and interaction network. Depending on the model system, it may participate in cell–cell communication, intracellular signaling, enzymatic processing, or regulation of gene expression programs. Mechanistic interpretation is often strengthened by considering upstream regulators and downstream readouts rather than relying on a single marker.\u003c\/p\u003e\u003cp\u003eExpression and abundance of Cga (Glycoprotein hormones alpha chain) QuickTest can vary by tissue, cell type, and physiological state. In many systems, levels are influenced by factors such as developmental stage, immune activation, metabolic status, and cellular stress. Because sample matrix and pre-analytical handling can affect measured concentrations, interpretation is typically strongest when experiments keep collection and processing consistent across groups.\u003c\/p\u003e\u003ch2\u003eNomenclature and related terms\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCga (Glycoprotein hormones alpha chain) QuickTest\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eGlycoprotein hormones alpha chain\u003c\/strong\u003e, \u003cstrong\u003eAnterior pituitary glycoprotein hormones common subunit alpha\u003c\/strong\u003e, and \u003cstrong\u003eFollicle-stimulating hormone alpha chain\u003c\/strong\u003e in the literature or in databases. When comparing results across studies, confirm that the reported analyte refers to the same molecule, species context, and molecular form (e.g., precursor vs mature protein, or soluble vs membrane-associated forms).\u003c\/p\u003e\u003ch2\u003eWhy it matters in research\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eUnderstanding how Cga (Glycoprotein hormones alpha chain) QuickTest relates to signal transduction, tissue homeostasis, stress responses, and disease-model biology in biomedical research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in Cga (Glycoprotein hormones alpha chain) QuickTest levels alongside other pathway components or complementary markers.\u003c\/li\u003e\n\u003cli\u003eConnecting molecular changes to phenotypes such as inflammation, remodeling, metabolism shifts, or cell-state transitions (context-dependent).\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eMolecular forms and interpretation\u003c\/h2\u003e\u003cp\u003eFor some targets, isoforms, proteolytic processing, or post-translational modifications (such as phosphorylation or glycosylation) can influence function and apparent abundance. If multiple molecular forms are expected in your model, align interpretation with the form most relevant to the biological question.\u003c\/p\u003e\u003ch2\u003eDisease and translational relevance\u003c\/h2\u003e\u003cp\u003eCga (Glycoprotein hormones alpha chain) QuickTest has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with biomedical studies. These associations are interpreted as research findings rather than diagnostic or therapeutic claims, and they should be evaluated alongside model-specific covariates and study design.\u003c\/p\u003e","brand":"Fine Test","offers":[{"title":"96 T","offer_id":52975498396013,"sku":"QT-EM0219-96T","price":585.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/quicktest_1c36e72e-c583-480c-a4e3-d6a8f205b887.jpg?v=1769600014"},{"product_id":"rat-cga-glycoprotein-hormones-alpha-chain-quicktest-elisa-kit-bhe10810458","title":"Rat Cga (Glycoprotein hormones alpha chain) QuickTest ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003erat Cga (Glycoprotein hormones alpha chain) QuickTest\u003c\/strong\u003e is a molecular target commonly studied in biomedical research. Hormones and endocrine mediators support long-range communication between organs and help maintain physiological homeostasis.\u003c\/p\u003e\u003ch2\u003eBiological role and mechanism\u003c\/h2\u003e\u003cp\u003eThe biological role of Cga (Glycoprotein hormones alpha chain) QuickTest is typically understood in terms of its molecular category and interaction network. Depending on the model system, it may participate in cell–cell communication, intracellular signaling, enzymatic processing, or regulation of gene expression programs. Mechanistic interpretation is often strengthened by considering upstream regulators and downstream readouts rather than relying on a single marker.\u003c\/p\u003e\u003cp\u003eExpression and abundance of Cga (Glycoprotein hormones alpha chain) QuickTest can vary by tissue, cell type, and physiological state. In many systems, levels are influenced by factors such as developmental stage, immune activation, metabolic status, and cellular stress. Because sample matrix and pre-analytical handling can affect measured concentrations, interpretation is typically strongest when experiments keep collection and processing consistent across groups.\u003c\/p\u003e\u003ch2\u003eNomenclature and related terms\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCga (Glycoprotein hormones alpha chain) QuickTest\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eGlycoprotein hormones alpha chain\u003c\/strong\u003e, \u003cstrong\u003eAnterior pituitary glycoprotein hormones common subunit alpha\u003c\/strong\u003e, and \u003cstrong\u003eFollicle-stimulating hormone alpha chain\u003c\/strong\u003e in the literature or in databases. When comparing results across studies, confirm that the reported analyte refers to the same molecule, species context, and molecular form (e.g., precursor vs mature protein, or soluble vs membrane-associated forms).\u003c\/p\u003e\u003ch2\u003eWhy it matters in research\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eUnderstanding how Cga (Glycoprotein hormones alpha chain) QuickTest relates to signal transduction, tissue homeostasis, stress responses, and disease-model biology in biomedical research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in Cga (Glycoprotein hormones alpha chain) QuickTest levels alongside other pathway components or complementary markers.\u003c\/li\u003e\n\u003cli\u003eConnecting molecular changes to phenotypes such as inflammation, remodeling, metabolism shifts, or cell-state transitions (context-dependent).\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eMolecular forms and interpretation\u003c\/h2\u003e\u003cp\u003eFor some targets, isoforms, proteolytic processing, or post-translational modifications (such as phosphorylation or glycosylation) can influence function and apparent abundance. If multiple molecular forms are expected in your model, align interpretation with the form most relevant to the biological question.\u003c\/p\u003e\u003ch2\u003eDisease and translational relevance\u003c\/h2\u003e\u003cp\u003eCga (Glycoprotein hormones alpha chain) QuickTest has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with biomedical studies. These associations are interpreted as research findings rather than diagnostic or therapeutic claims, and they should be evaluated alongside model-specific covariates and study design.\u003c\/p\u003e","brand":"Fine Test","offers":[{"title":"96 T","offer_id":52975502164333,"sku":"QT-ER0088-96T","price":585.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/quicktest_d781d4a1-a160-48db-bde5-2c4990f22720.jpg?v=1769600054"},{"product_id":"human-lhcgr-lutropin-choriogonadotropic-hormone-receptor-quicktest-elisa-kit-bhe10811513","title":"Human LHCGR (Lutropin-choriogonadotropic hormone receptor) QuickTest ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ehuman LHCGR (Lutropin-choriogonadotropic hormone receptor) QuickTest\u003c\/strong\u003e is a molecular target commonly studied in biomedical research. Receptors translate extracellular cues into intracellular signaling programs and may be regulated through expression, ligand binding, shedding, and endocytosis.\u003c\/p\u003e\u003ch2\u003eBiological role and mechanism\u003c\/h2\u003e\u003cp\u003eThe biological role of LHCGR (Lutropin-choriogonadotropic hormone receptor) QuickTest is typically understood in terms of its molecular category and interaction network. Depending on the model system, it may participate in cell–cell communication, intracellular signaling, enzymatic processing, or regulation of gene expression programs. Mechanistic interpretation is often strengthened by considering upstream regulators and downstream readouts rather than relying on a single marker.\u003c\/p\u003e\u003cp\u003eExpression and abundance of LHCGR (Lutropin-choriogonadotropic hormone receptor) QuickTest can vary by tissue, cell type, and physiological state. In many systems, levels are influenced by factors such as developmental stage, immune activation, metabolic status, and cellular stress. Because sample matrix and pre-analytical handling can affect measured concentrations, interpretation is typically strongest when experiments keep collection and processing consistent across groups.\u003c\/p\u003e\u003ch2\u003eNomenclature and related terms\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eLHCGR (Lutropin-choriogonadotropic hormone receptor) QuickTest\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eLHCGR\u003c\/strong\u003e, \u003cstrong\u003eLutropin-choriogonadotropic hormone receptor\u003c\/strong\u003e, and \u003cstrong\u003eLuteinizing hormone receptor\u003c\/strong\u003e in the literature or in databases. When comparing results across studies, confirm that the reported analyte refers to the same molecule, species context, and molecular form (e.g., precursor vs mature protein, or soluble vs membrane-associated forms).\u003c\/p\u003e\u003ch2\u003eWhy it matters in research\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eUnderstanding how LHCGR (Lutropin-choriogonadotropic hormone receptor) QuickTest relates to signal transduction, tissue homeostasis, stress responses, and disease-model biology in biomedical research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in LHCGR (Lutropin-choriogonadotropic hormone receptor) QuickTest levels alongside other pathway components or complementary markers.\u003c\/li\u003e\n\u003cli\u003eConnecting molecular changes to phenotypes such as inflammation, remodeling, metabolism shifts, or cell-state transitions (context-dependent).\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eMolecular forms and interpretation\u003c\/h2\u003e\u003cp\u003eFor some targets, isoforms, proteolytic processing, or post-translational modifications (such as phosphorylation or glycosylation) can influence function and apparent abundance. If multiple molecular forms are expected in your model, align interpretation with the form most relevant to the biological question.\u003c\/p\u003e\u003ch2\u003eDisease and translational relevance\u003c\/h2\u003e\u003cp\u003eLHCGR (Lutropin-choriogonadotropic hormone receptor) QuickTest has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with biomedical studies. These associations are interpreted as research findings rather than diagnostic or therapeutic claims, and they should be evaluated alongside model-specific covariates and study design.\u003c\/p\u003e","brand":"Fine Test","offers":[{"title":"96 T","offer_id":52975539061101,"sku":"QT-EH1592-96T","price":585.0,"currency_code":"USD","in_stock":true}]},{"product_id":"human-hcg-human-chorionic-gonadotropin-elisa-kit-bhe10812245","title":"Human hCG (human Chorionic Gonadotropin) ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ehuman hCG (human Chorionic Gonadotropin)\u003c\/strong\u003e is a molecular target commonly studied in biomedical research. Many proteins are studied as molecular readouts that can change with cellular state, tissue remodeling, or stress responses.\u003c\/p\u003e\u003ch2\u003eBiological role and mechanism\u003c\/h2\u003e\u003cp\u003eThe biological role of hCG is typically understood in terms of its molecular category and interaction network. Depending on the model system, it may participate in cell–cell communication, intracellular signaling, enzymatic processing, or regulation of gene expression programs. Mechanistic interpretation is often strengthened by considering upstream regulators and downstream readouts rather than relying on a single marker.\u003c\/p\u003e\u003cp\u003eExpression and abundance of hCG can vary by tissue, cell type, and physiological state. In many systems, levels are influenced by factors such as developmental stage, immune activation, metabolic status, and cellular stress. Because sample matrix and pre-analytical handling can affect measured concentrations, interpretation is typically strongest when experiments keep collection and processing consistent across groups.\u003c\/p\u003e\u003ch2\u003eNomenclature and related terms\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ehCG (human Chorionic Gonadotropin)\u003c\/strong\u003e may also be referenced as \u003cstrong\u003ehCG\u003c\/strong\u003e and \u003cstrong\u003ehuman Chorionic Gonadotropin\u003c\/strong\u003e in the literature or in databases. When comparing results across studies, confirm that the reported analyte refers to the same molecule, species context, and molecular form (e.g., precursor vs mature protein, or soluble vs membrane-associated forms).\u003c\/p\u003e\u003ch2\u003eWhy it matters in research\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eUnderstanding how hCG relates to signal transduction, tissue homeostasis, stress responses, and disease-model biology in biomedical research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in hCG levels alongside other pathway components or complementary markers.\u003c\/li\u003e\n\u003cli\u003eConnecting molecular changes to phenotypes such as inflammation, remodeling, metabolism shifts, or cell-state transitions (context-dependent).\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eMolecular forms and interpretation\u003c\/h2\u003e\u003cp\u003eFor some targets, isoforms, proteolytic processing, or post-translational modifications (such as phosphorylation or glycosylation) can influence function and apparent abundance. If multiple molecular forms are expected in your model, align interpretation with the form most relevant to the biological question.\u003c\/p\u003e\u003ch2\u003eDisease and translational relevance\u003c\/h2\u003e\u003cp\u003ehCG has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with biomedical studies. These associations are interpreted as research findings rather than diagnostic or therapeutic claims, and they should be evaluated alongside model-specific covariates and study design.\u003c\/p\u003e","brand":"Fine Test","offers":[{"title":"96 T","offer_id":52975570125165,"sku":"EH5502-96T","price":520.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_22a2430d-ecd7-48a8-ae1d-0022a6e8608e.jpg?v=1769600694"},{"product_id":"recombinant-mouse-prlr-protein-c-fc-bhp21400761","title":"Recombinant Mouse PRLR Protein, C-Fc","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eTarget identity:\u003c\/strong\u003e\u003cstrong\u003ePRLR\u003c\/strong\u003e is a protein. It is typically cell-type and isoform dependent (intracellular or extracellular).\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003ePRLR\u003c\/strong\u003e is provided as a recombinant protein reagent for \u003cstrong\u003eresearch use only\u003c\/strong\u003e. Recombinant proteins are commonly used as defined molecular inputs in biochemical and cell-free systems, enabling controlled interrogation of binding, activity, and pathway-relevant interactions.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eProtein identity context:\u003c\/strong\u003e PRLR (expression region Gln20-Asp229; approx. molecular weight 52.92 kDa).\u003c\/p\u003e\u003ch2\u003eBiological significance and function\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ePRLR\u003c\/strong\u003e is used in RUO research to interrogate molecular mechanisms, interaction networks, and pathway-linked phenotypes in experimental systems. This target is frequently explored in \u003cstrong\u003eMolecular \u0026amp; Cellular Biology\u003c\/strong\u003e research contexts.\u003c\/p\u003e\u003ch2\u003eMolecular characteristics\u003c\/h2\u003e\u003cp\u003eKey molecular attributes can influence binding behavior, stability, and assay background—especially for multimeric, disulfide-rich, or PTM-dependent targets.\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eExpression system:\u003c\/strong\u003e Mammalian Cells\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eExpression region:\u003c\/strong\u003e Gln20-Asp229\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eMolecular weight:\u003c\/strong\u003e 52.92 kDa\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePurity:\u003c\/strong\u003e \u0026gt;95%\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eForm:\u003c\/strong\u003e Lyophilized\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eFormulation:\u003c\/strong\u003e Lyophilized from a solution in PBS pH 7.4, 1 mM EDTA, 4% Trehalose, 1% Mannitol.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003ePost-translational considerations:\u003c\/strong\u003e Mammalian expression can support native-like folding, disulfide bond formation, and glycosylation. These features can be important for secreted proteins and receptor-binding interactions.\u003c\/p\u003e\u003ch2\u003eExpression and purification strategy\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eExpression system:\u003c\/strong\u003e Mammalian Cells. Expression host selection can influence folding and PTM state, which may affect activity or binding in different assay formats.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003ePurification:\u003c\/strong\u003e Affinity-chromatography. Purification approach and formulation influence sample homogeneity and background signal in downstream biochemical measurements.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eEndotoxin consideration:\u003c\/strong\u003e Reported endotoxin level is Please contact with the lab for this information.; this parameter can matter when recombinant proteins are used in cell-based systems sensitive to innate immune activation.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eReconstitution:\u003c\/strong\u003e Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details..\u003c\/p\u003e\u003ch2\u003eResearch interpretation\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eResearch interpretation:\u003c\/strong\u003e Recombinant protein reagents support controlled experiments such as interaction mapping, assay calibration, and reconstitution studies with defined inputs. Interpreting outcomes typically benefits from pairing the primary readout with orthogonal markers that report pathway state and complex formation.\u003c\/p\u003e","brand":"Biohippo Inc","offers":[{"title":"100 ug","offer_id":53000698528109,"sku":"MB801011-100UG","price":478.0,"currency_code":"USD","in_stock":true},{"title":"1 mg","offer_id":53000698560877,"sku":"MB801011-1MG","price":2878.0,"currency_code":"USD","in_stock":true}]},{"product_id":"recombinant-mouse-prl-protein-n-his-bhp21404032","title":"Recombinant Mouse PRL Protein, N-His","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eTarget identity:\u003c\/strong\u003e\u003cstrong\u003ePRL\u003c\/strong\u003e is a protein. It is typically cell-type and isoform dependent (intracellular or extracellular).\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003ePRL\u003c\/strong\u003e is provided as a recombinant protein reagent for \u003cstrong\u003eresearch use only\u003c\/strong\u003e. Recombinant proteins are commonly used as defined molecular inputs in biochemical and cell-free systems, enabling controlled interrogation of binding, activity, and pathway-relevant interactions.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eProtein identity context:\u003c\/strong\u003e PRL (expression region Leu30-Cys226; approx. molecular weight 24.71 kDa).\u003c\/p\u003e\u003ch2\u003eBiological significance and function\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ePRL\u003c\/strong\u003e is used in RUO research to interrogate molecular mechanisms, interaction networks, and pathway-linked phenotypes in experimental systems. This target is frequently explored in \u003cstrong\u003eMolecular \u0026amp; Cellular Biology\u003c\/strong\u003e research contexts.\u003c\/p\u003e\u003ch2\u003eMolecular characteristics\u003c\/h2\u003e\u003cp\u003eKey molecular attributes can influence binding behavior, stability, and assay background—especially for multimeric, disulfide-rich, or PTM-dependent targets.\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eExpression system:\u003c\/strong\u003e E. coli\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eExpression region:\u003c\/strong\u003e Leu30-Cys226\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eMolecular weight:\u003c\/strong\u003e 24.71 kDa\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePurity:\u003c\/strong\u003e \u0026gt;90%\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eForm:\u003c\/strong\u003e Lyophilized\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eFormulation:\u003c\/strong\u003e Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1 mM EDTA, 4% Trehalose, 1% Mannitol.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003ePost-translational considerations:\u003c\/strong\u003e Prokaryotic expression typically yields a non-glycosylated recombinant form. This is often appropriate for many intracellular proteins and binding studies, while disulfide-rich or PTM-dependent extracellular targets may behave differently when native PTMs are required.\u003c\/p\u003e\u003ch2\u003eExpression and purification strategy\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eExpression system:\u003c\/strong\u003e E. coli. Expression host selection can influence folding and PTM state, which may affect activity or binding in different assay formats.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003ePurification:\u003c\/strong\u003e Affinity-chromatography. Purification approach and formulation influence sample homogeneity and background signal in downstream biochemical measurements.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eEndotoxin consideration:\u003c\/strong\u003e Reported endotoxin level is Please contact with the lab for this information.; this parameter can matter when recombinant proteins are used in cell-based systems sensitive to innate immune activation.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eReconstitution:\u003c\/strong\u003e Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details..\u003c\/p\u003e\u003ch2\u003eResearch interpretation\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eResearch interpretation:\u003c\/strong\u003e Recombinant protein reagents support controlled experiments such as interaction mapping, assay calibration, and reconstitution studies with defined inputs. Interpreting outcomes typically benefits from pairing the primary readout with orthogonal markers that report pathway state and complex formation.\u003c\/p\u003e","brand":"Biohippo Inc","offers":[{"title":"100 ug","offer_id":53000984494445,"sku":"MF817012-100UG","price":311.0,"currency_code":"USD","in_stock":true},{"title":"1 mg","offer_id":53000984527213,"sku":"MF817012-1MG","price":1627.0,"currency_code":"USD","in_stock":true}]},{"product_id":"recombinant-human-lhcgr-protein-n-his-bhp21405572","title":"Recombinant Human LHCGR Protein, N-His","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eTarget identity:\u003c\/strong\u003e\u003cstrong\u003eLHCGR\u003c\/strong\u003e is a protein. It is typically cell-type and isoform dependent (intracellular or extracellular).\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eLHCGR\u003c\/strong\u003e is provided as a recombinant protein reagent for \u003cstrong\u003eresearch use only\u003c\/strong\u003e. Recombinant proteins are commonly used as defined molecular inputs in biochemical and cell-free systems, enabling controlled interrogation of binding, activity, and pathway-relevant interactions.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eProtein identity context:\u003c\/strong\u003e LHCGR (expression region Arg43-Phe265; approx. molecular weight 27.04 kDa).\u003c\/p\u003e\u003ch2\u003eBiological significance and function\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eLHCGR\u003c\/strong\u003e is used in RUO research to interrogate molecular mechanisms, interaction networks, and pathway-linked phenotypes in experimental systems. This target is frequently explored in \u003cstrong\u003eMolecular \u0026amp; Cellular Biology\u003c\/strong\u003e research contexts.\u003c\/p\u003e\u003ch2\u003eMolecular characteristics\u003c\/h2\u003e\u003cp\u003eKey molecular attributes can influence binding behavior, stability, and assay background—especially for multimeric, disulfide-rich, or PTM-dependent targets.\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eExpression system:\u003c\/strong\u003e E. coli\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eExpression region:\u003c\/strong\u003e Arg43-Phe265\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eMolecular weight:\u003c\/strong\u003e 27.04 kDa\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePurity:\u003c\/strong\u003e \u0026gt;90%\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eForm:\u003c\/strong\u003e Lyophilized\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eFormulation:\u003c\/strong\u003e Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1 mM EDTA, 4% Trehalose, 1% Mannitol.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003ePost-translational considerations:\u003c\/strong\u003e Prokaryotic expression typically yields a non-glycosylated recombinant form. This is often appropriate for many intracellular proteins and binding studies, while disulfide-rich or PTM-dependent extracellular targets may behave differently when native PTMs are required.\u003c\/p\u003e\u003ch2\u003eExpression and purification strategy\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eExpression system:\u003c\/strong\u003e E. coli. Expression host selection can influence folding and PTM state, which may affect activity or binding in different assay formats.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003ePurification:\u003c\/strong\u003e Affinity-chromatography. Purification approach and formulation influence sample homogeneity and background signal in downstream biochemical measurements.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eEndotoxin consideration:\u003c\/strong\u003e Reported endotoxin level is Please contact with the lab for this information.; this parameter can matter when recombinant proteins are used in cell-based systems sensitive to innate immune activation.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eReconstitution:\u003c\/strong\u003e Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details..\u003c\/p\u003e\u003ch2\u003eResearch interpretation\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eResearch interpretation:\u003c\/strong\u003e Recombinant protein reagents support controlled experiments such as interaction mapping, assay calibration, and reconstitution studies with defined inputs. Interpreting outcomes typically benefits from pairing the primary readout with orthogonal markers that report pathway state and complex formation.\u003c\/p\u003e","brand":"Biohippo Inc","offers":[{"title":"100 ug","offer_id":53001121988973,"sku":"HB699012-100UG","price":311.0,"currency_code":"USD","in_stock":true},{"title":"1 mg","offer_id":53001122021741,"sku":"HB699012-1MG","price":1627.0,"currency_code":"USD","in_stock":true}]},{"product_id":"recombinant-human-prlr-protein-c-his-bhp21406065","title":"Recombinant Human PRLR Protein, C-His","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eTarget identity:\u003c\/strong\u003e\u003cstrong\u003ePRLR\u003c\/strong\u003e is a protein. It is typically cell-type and isoform dependent (intracellular or extracellular).\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003ePRLR\u003c\/strong\u003e is provided as a recombinant protein reagent for \u003cstrong\u003eresearch use only\u003c\/strong\u003e. Recombinant proteins are commonly used as defined molecular inputs in biochemical and cell-free systems, enabling controlled interrogation of binding, activity, and pathway-relevant interactions.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eProtein identity context:\u003c\/strong\u003e PRLR (expression region Met1-Asp234; approx. molecular weight 27.98 kDa).\u003c\/p\u003e\u003ch2\u003eBiological significance and function\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ePRLR\u003c\/strong\u003e is used in RUO research to interrogate molecular mechanisms, interaction networks, and pathway-linked phenotypes in experimental systems. This target is frequently explored in \u003cstrong\u003eMolecular \u0026amp; Cellular Biology\u003c\/strong\u003e research contexts.\u003c\/p\u003e\u003ch2\u003eMolecular characteristics\u003c\/h2\u003e\u003cp\u003eKey molecular attributes can influence binding behavior, stability, and assay background—especially for multimeric, disulfide-rich, or PTM-dependent targets.\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eExpression system:\u003c\/strong\u003e Mammalian Cells\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eExpression region:\u003c\/strong\u003e Met1-Asp234\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eMolecular weight:\u003c\/strong\u003e 27.98 kDa\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePurity:\u003c\/strong\u003e \u0026gt;95%\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eForm:\u003c\/strong\u003e Lyophilized\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eFormulation:\u003c\/strong\u003e Lyophilized from a solution in PBS pH 7.4, 1 mM EDTA, 4% Trehalose, 1% Mannitol.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003ePost-translational considerations:\u003c\/strong\u003e Mammalian expression can support native-like folding, disulfide bond formation, and glycosylation. These features can be important for secreted proteins and receptor-binding interactions.\u003c\/p\u003e\u003ch2\u003eExpression and purification strategy\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eExpression system:\u003c\/strong\u003e Mammalian Cells. Expression host selection can influence folding and PTM state, which may affect activity or binding in different assay formats.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003ePurification:\u003c\/strong\u003e Affinity-chromatography. Purification approach and formulation influence sample homogeneity and background signal in downstream biochemical measurements.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eEndotoxin consideration:\u003c\/strong\u003e Reported endotoxin level is Please contact with the lab for this information.; this parameter can matter when recombinant proteins are used in cell-based systems sensitive to innate immune activation.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eReconstitution:\u003c\/strong\u003e Reconstitute in sterile water for a stock solution.A copy of datasheet will be provided with the products, please refer to it for details..\u003c\/p\u003e\u003ch2\u003eResearch interpretation\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eResearch interpretation:\u003c\/strong\u003e Recombinant protein reagents support controlled experiments such as interaction mapping, assay calibration, and reconstitution studies with defined inputs. Interpreting outcomes typically benefits from pairing the primary readout with orthogonal markers that report pathway state and complex formation.\u003c\/p\u003e","brand":"Biohippo Inc","offers":[{"title":"100 ug","offer_id":53001186214253,"sku":"HB801011-100UG","price":478.0,"currency_code":"USD","in_stock":true},{"title":"1 mg","offer_id":53001186247021,"sku":"HB801011-1MG","price":2878.0,"currency_code":"USD","in_stock":true}]},{"product_id":"recombinant-human-prlr-protein-n-his-bhp21408830","title":"Recombinant Human PRLR Protein, N-His","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eTarget identity:\u003c\/strong\u003e\u003cstrong\u003ePRLR\u003c\/strong\u003e is a protein. It is typically cell-type and isoform dependent (intracellular or extracellular).\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003ePRLR\u003c\/strong\u003e is provided as a recombinant protein reagent for \u003cstrong\u003eresearch use only\u003c\/strong\u003e. Recombinant proteins are commonly used as defined molecular inputs in biochemical and cell-free systems, enabling controlled interrogation of binding, activity, and pathway-relevant interactions.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eProtein identity context:\u003c\/strong\u003e PRLR (expression region Gln25-Asp234; approx. molecular weight 26.73 kDa).\u003c\/p\u003e\u003ch2\u003eBiological significance and function\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ePRLR\u003c\/strong\u003e is used in RUO research to interrogate molecular mechanisms, interaction networks, and pathway-linked phenotypes in experimental systems. This target is frequently explored in \u003cstrong\u003eMolecular \u0026amp; Cellular Biology\u003c\/strong\u003e research contexts.\u003c\/p\u003e\u003ch2\u003eMolecular characteristics\u003c\/h2\u003e\u003cp\u003eKey molecular attributes can influence binding behavior, stability, and assay background—especially for multimeric, disulfide-rich, or PTM-dependent targets.\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eExpression system:\u003c\/strong\u003e E. coli\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eExpression region:\u003c\/strong\u003e Gln25-Asp234\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eMolecular weight:\u003c\/strong\u003e 26.73 kDa\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePurity:\u003c\/strong\u003e \u0026gt;90%\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eForm:\u003c\/strong\u003e Lyophilized\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eFormulation:\u003c\/strong\u003e Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1 mM EDTA, 4% Trehalose, 1% Mannitol.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003ePost-translational considerations:\u003c\/strong\u003e Prokaryotic expression typically yields a non-glycosylated recombinant form. This is often appropriate for many intracellular proteins and binding studies, while disulfide-rich or PTM-dependent extracellular targets may behave differently when native PTMs are required.\u003c\/p\u003e\u003ch2\u003eExpression and purification strategy\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eExpression system:\u003c\/strong\u003e E. coli. Expression host selection can influence folding and PTM state, which may affect activity or binding in different assay formats.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003ePurification:\u003c\/strong\u003e Affinity-chromatography. Purification approach and formulation influence sample homogeneity and background signal in downstream biochemical measurements.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eEndotoxin consideration:\u003c\/strong\u003e Reported endotoxin level is Please contact with the lab for this information.; this parameter can matter when recombinant proteins are used in cell-based systems sensitive to innate immune activation.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eReconstitution:\u003c\/strong\u003e Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details..\u003c\/p\u003e\u003ch2\u003eResearch interpretation\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eResearch interpretation:\u003c\/strong\u003e Recombinant protein reagents support controlled experiments such as interaction mapping, assay calibration, and reconstitution studies with defined inputs. Interpreting outcomes typically benefits from pairing the primary readout with orthogonal markers that report pathway state and complex formation.\u003c\/p\u003e","brand":"Biohippo Inc","offers":[{"title":"100 ug","offer_id":53001715253613,"sku":"HB801012-100UG","price":311.0,"currency_code":"USD","in_stock":true},{"title":"1 mg","offer_id":53001715286381,"sku":"HB801012-1MG","price":1627.0,"currency_code":"USD","in_stock":true}]},{"product_id":"recombinant-human-cgb3-protein-n-his-bhp21409064","title":"Recombinant Human CGB3 Protein, N-His","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eTarget identity:\u003c\/strong\u003e\u003cstrong\u003eCGB3\u003c\/strong\u003e is a protein. It is typically cell-type and isoform dependent (intracellular or extracellular).\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eCGB3\u003c\/strong\u003e is provided as a recombinant protein reagent for \u003cstrong\u003eresearch use only\u003c\/strong\u003e. Recombinant proteins are commonly used as defined molecular inputs in biochemical and cell-free systems, enabling controlled interrogation of binding, activity, and pathway-relevant interactions.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eProtein identity context:\u003c\/strong\u003e CGB3 (expression region Pro31-Gln165; approx. molecular weight 16.62 kDa).\u003c\/p\u003e\u003ch2\u003eBiological significance and function\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eCGB3\u003c\/strong\u003e is used in RUO research to interrogate molecular mechanisms, interaction networks, and pathway-linked phenotypes in experimental systems. This target is frequently explored in \u003cstrong\u003eMolecular \u0026amp; Cellular Biology\u003c\/strong\u003e research contexts.\u003c\/p\u003e\u003ch2\u003eMolecular characteristics\u003c\/h2\u003e\u003cp\u003eKey molecular attributes can influence binding behavior, stability, and assay background—especially for multimeric, disulfide-rich, or PTM-dependent targets.\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eExpression system:\u003c\/strong\u003e E. coli\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eExpression region:\u003c\/strong\u003e Pro31-Gln165\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eMolecular weight:\u003c\/strong\u003e 16.62 kDa\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePurity:\u003c\/strong\u003e \u0026gt;90%\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eForm:\u003c\/strong\u003e Lyophilized\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eFormulation:\u003c\/strong\u003e Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1 mM EDTA, 4% Trehalose, 1% Mannitol.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003ePost-translational considerations:\u003c\/strong\u003e Prokaryotic expression typically yields a non-glycosylated recombinant form. This is often appropriate for many intracellular proteins and binding studies, while disulfide-rich or PTM-dependent extracellular targets may behave differently when native PTMs are required.\u003c\/p\u003e\u003ch2\u003eExpression and purification strategy\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eExpression system:\u003c\/strong\u003e E. coli. Expression host selection can influence folding and PTM state, which may affect activity or binding in different assay formats.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003ePurification:\u003c\/strong\u003e Affinity-chromatography. Purification approach and formulation influence sample homogeneity and background signal in downstream biochemical measurements.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eEndotoxin consideration:\u003c\/strong\u003e Reported endotoxin level is Please contact with the lab for this information.; this parameter can matter when recombinant proteins are used in cell-based systems sensitive to innate immune activation.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eReconstitution:\u003c\/strong\u003e Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details..\u003c\/p\u003e\u003ch2\u003eResearch interpretation\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eResearch interpretation:\u003c\/strong\u003e Recombinant protein reagents support controlled experiments such as interaction mapping, assay calibration, and reconstitution studies with defined inputs. Interpreting outcomes typically benefits from pairing the primary readout with orthogonal markers that report pathway state and complex formation.\u003c\/p\u003e","brand":"Biohippo Inc","offers":[{"title":"100 ug","offer_id":53001749561709,"sku":"HY330012-100UG","price":311.0,"currency_code":"USD","in_stock":true},{"title":"1 mg","offer_id":53001749594477,"sku":"HY330012-1MG","price":1627.0,"currency_code":"USD","in_stock":true}]}],"url":"https:\/\/www.ebiohippo.com\/collections\/rs-prolactin-hcg-markers.oembed?page=3","provider":"BioHippo","version":"1.0","type":"link"}