{"title":"TDP-43 \/ FUS \/ ALS Markers","description":null,"products":[{"product_id":"bovine-superoxide-dismutase-cu-zn-sod1-elisa-kit-bhe12100443","title":"Bovine Superoxide Dismutase (Cu-Zn), SOD1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eSuperoxide Dismutase (Cu-Zn) (SOD1)\u003c\/strong\u003e is a molecular target commonly studied in metabolism 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: P00442\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Superoxide Dismutase (Cu-Zn) (SOD1) is frequently examined in relation to energy homeostasis, glucose and lipid metabolism, and insulin sensitivity and endocrine regulation. 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 Superoxide Dismutase (Cu-Zn) (SOD1) 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\u003eSuperoxide Dismutase (Cu-Zn) (SOD1) 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 Superoxide Dismutase (Cu-Zn) (SOD1) 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\u003eSuperoxide Dismutase (Cu-Zn) (SOD1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eSOD 1\u003c\/strong\u003e, \u003cstrong\u003eSOD1\u003c\/strong\u003e, and \u003cstrong\u003eSuperoxide dismutase [Cu-Zn\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":52952447615341,"sku":"E2070Bo-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2070Bo.jpg?v=1769145937"},{"product_id":"canine-superoxide-dismutase-cu-zn-sod1-elisa-kit-bhe12100881","title":"Canine Superoxide Dismutase (Cu-Zn), SOD1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eSuperoxide Dismutase (Cu-Zn) (SOD1)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction, cell biology, 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: Q8WNN6\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Superoxide Dismutase (Cu-Zn) (SOD1) is frequently examined in relation to signal transduction pathways, cell cycle and stress-response programs, and organelle and membrane dynamics. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Superoxide Dismutase (Cu-Zn) (SOD1) 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\u003eSuperoxide Dismutase (Cu-Zn) (SOD1) 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 Superoxide Dismutase (Cu-Zn) (SOD1) 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\u003eSuperoxide Dismutase (Cu-Zn) (SOD1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eSOD1\u003c\/strong\u003e and \u003cstrong\u003eSuperoxide dismutase [Cu-Zn\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":52952451973485,"sku":"E0373Ca-96T","price":475.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0373Ca.jpg?v=1769145977"},{"product_id":"horse-superoxide-dismutase-cu-zn-sod1-elisa-kit-bhe12101676","title":"Horse Superoxide Dismutase(Cu-Zn), SOD1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eHorse Superoxide Dismutase(Cu-Zn) (SOD1)\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: P00443\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Horse Superoxide Dismutase(Cu-Zn) (SOD1) 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 Horse Superoxide Dismutase(Cu-Zn) (SOD1) 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\u003eHorse Superoxide Dismutase(Cu-Zn) (SOD1) 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 Horse Superoxide Dismutase(Cu-Zn) (SOD1) 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\u003eHorse Superoxide Dismutase(Cu-Zn) (SOD1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eCU\/ZN-SOD\u003c\/strong\u003e, \u003cstrong\u003eSOD1\u003c\/strong\u003e, and \u003cstrong\u003eSuperoxide dismutase Cu-Zn\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":52952453808493,"sku":"E0054HO-96T","price":498.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0054HO.jpg?v=1769145990"},{"product_id":"human-tar-dna-binding-protein-43-tdp-43-elisa-kit-bhe12102037","title":"Human Tar DNA Binding Protein 43, TDP-43 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eTar DNA Binding Protein 43 (TARDBP)\u003c\/strong\u003e is a molecular target commonly studied in microbiology, neuroscience, and epigenetics and nuclear signaling research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q13148\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Tar DNA Binding Protein 43 (TARDBP) is frequently examined in relation to infection and host defense, barrier and mucosal immunity, and host–microbe interactions. 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 Tar DNA Binding Protein 43 (TARDBP) 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\u003eTar DNA Binding Protein 43 (TARDBP) 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 Tar DNA Binding Protein 43 (TARDBP) 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\u003eTar DNA Binding Protein 43 (TARDBP)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eALS10\u003c\/strong\u003e, \u003cstrong\u003eTAR DNA-binding protein 43\u003c\/strong\u003e, and \u003cstrong\u003eTARDBP\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":52952458821997,"sku":"E0333Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0333Hu.jpg?v=1769146042"},{"product_id":"human-optineurin-optn-elisa-kit-bhe12105059","title":"Human Optineurin, OPTN ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eOptineurin (OPTN)\u003c\/strong\u003e is a molecular target commonly studied in immunology and 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: Q96CV9\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Optineurin (OPTN) is frequently examined in relation to innate and adaptive immune responses, cytokine signaling networks, and immune cell activation and trafficking. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Optineurin (OPTN) 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\u003eOptineurin (OPTN) 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 Optineurin (OPTN) 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\u003eOptineurin (OPTN)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eE3-14.7K-interacting protein\u003c\/strong\u003e, \u003cstrong\u003eFIP-2\u003c\/strong\u003e, and \u003cstrong\u003eHIP-7\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":52952505975149,"sku":"E3579Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E3579Hu.jpg?v=1769146450"},{"product_id":"human-uncharacterized-protein-c9orf72-c9orf72-elisa-kit-bhe12105385","title":"Human Uncharacterized Protein C9Orf72, C9ORF72 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eC9orf72\u003c\/strong\u003e is a molecular target commonly studied in neuroscience research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: A6NCS6\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, C9orf72 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 C9orf72 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\u003eC9orf72 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 C9orf72 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\u003eC9orf72\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eC9orf72\u003c\/strong\u003e and \u003cstrong\u003eUncharacterized protein C2orf72\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":52952515510637,"sku":"E3951Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E3951Hu.jpg?v=1769146496"},{"product_id":"human-superoxide-dismutase-cu-zn-sod1-elisa-kit-bhe12105830","title":"Human Superoxide Dismutase (Cu-Zn), SOD1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eSuperoxide Dismutase (Cu-Zn) (SOD1)\u003c\/strong\u003e is a molecular target commonly studied in metabolism 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: P00441\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Superoxide Dismutase (Cu-Zn) (SOD1) is frequently examined in relation to energy homeostasis, glucose and lipid metabolism, and insulin sensitivity and endocrine regulation. 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 Superoxide Dismutase (Cu-Zn) (SOD1) 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\u003eSuperoxide Dismutase (Cu-Zn) (SOD1) 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 Superoxide Dismutase (Cu-Zn) (SOD1) 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\u003eSuperoxide Dismutase (Cu-Zn) (SOD1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003ehSod1\u003c\/strong\u003e, \u003cstrong\u003eSOD 1\u003c\/strong\u003e, and \u003cstrong\u003eSOD1\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":52952529863021,"sku":"E4502Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E4502Hu.jpg?v=1769146545"},{"product_id":"human-tar-dna-binding-protein-43-tardbp-elisa-kit-bhe12107608","title":"Human Tar DNA-binding Protein 43, TARDBP ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eTar DNA-binding Protein 43 (TARDBP)\u003c\/strong\u003e is a molecular target commonly studied in microbiology, neuroscience, and epigenetics and nuclear signaling research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q13148\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Tar DNA-binding Protein 43 (TARDBP) is frequently examined in relation to infection and host defense, barrier and mucosal immunity, and host–microbe interactions. 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 Tar DNA-binding Protein 43 (TARDBP) 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\u003eTar DNA-binding Protein 43 (TARDBP) 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 Tar DNA-binding Protein 43 (TARDBP) 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\u003eTar DNA-binding Protein 43 (TARDBP)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eALS10\u003c\/strong\u003e, \u003cstrong\u003eTAR DNA-binding protein 43\u003c\/strong\u003e, and \u003cstrong\u003eTARDBP\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":52952603754861,"sku":"E6246Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E6246Hu.jpg?v=1769146933"},{"product_id":"rat-superoxide-dismutase-cu-zn-sod1-elisa-kit-bhe12112676","title":"Rat Superoxide Dismutase, Cu-Zn, SOD1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eSuperoxide Dismutase, Cu-Zn (SOD1)\u003c\/strong\u003e is a molecular target commonly studied in metabolism 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: P07632\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Superoxide Dismutase, Cu-Zn (SOD1) is frequently examined in relation to energy homeostasis, glucose and lipid metabolism, and insulin sensitivity and endocrine regulation. 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 Superoxide Dismutase, Cu-Zn (SOD1) 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\u003eSuperoxide Dismutase, Cu-Zn (SOD1) 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 Superoxide Dismutase, Cu-Zn (SOD1) 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\u003eSuperoxide Dismutase, Cu-Zn (SOD1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eSOD 1\u003c\/strong\u003e, \u003cstrong\u003eSOD1\u003c\/strong\u003e, and \u003cstrong\u003eSuperoxide dismutase [Cu-Zn\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":52952690524525,"sku":"E1444Ra-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E1444Ra.jpg?v=1769147445"},{"product_id":"sheep-superoxide-dismutase-cu-zn-sod1-elisa-kit-bhe12113651","title":"Sheep Superoxide Dismutase (Cu-Zn), SOD1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eSuperoxide Dismutase (Cu-Zn) (SOD1)\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: P09670\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Superoxide Dismutase (Cu-Zn) (SOD1) 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 Superoxide Dismutase (Cu-Zn) (SOD1) 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\u003eSuperoxide Dismutase (Cu-Zn) (SOD1) 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 Superoxide Dismutase (Cu-Zn) (SOD1) 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\u003eSuperoxide Dismutase (Cu-Zn) (SOD1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eSOD1\u003c\/strong\u003e and \u003cstrong\u003eSuperoxide dismutase Cu-Zn\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":52952714281325,"sku":"E0183Sh-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E0183Sh.jpg?v=1769147576"},{"product_id":"human-sequestosome-1-sqstm1-elisa-kit-bhe12115289","title":"Human Sequestosome-1, SQSTM1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eSequestosome-1 (SQSTM1)\u003c\/strong\u003e is a molecular target commonly studied in signal transduction, epigenetics and nuclear signaling, and cardiovascular research. This molecule is commonly investigated as part of broader signaling, regulatory, or homeostatic networks.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q13501\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Sequestosome-1 (SQSTM1) is frequently examined in relation to vascular biology and endothelial function, cardiac remodeling and injury responses, and hemostasis and thrombosis. Depending on the model system, changes in abundance can be associated with shifts in signaling state, cellular composition, or tissue physiology.\u003c\/p\u003e\u003ch2\u003eExpression and regulation\u003c\/h2\u003e\u003cp\u003eExpression of Sequestosome-1 (SQSTM1) 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\u003eSequestosome-1 (SQSTM1) 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 Sequestosome-1 (SQSTM1) 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\u003eSequestosome-1 (SQSTM1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eA170\u003c\/strong\u003e, \u003cstrong\u003eDMRV\u003c\/strong\u003e, and \u003cstrong\u003eEBI3-associated protein of 60 kDa\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":52952721326445,"sku":"E6779Hu-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E6779Hu.jpg?v=1769147608"},{"product_id":"mouse-superoxide-dismutase-cu-zn-sod1-elisa-kit-bhe12115415","title":"Mouse Superoxide Dismutase, Cu-Zn, SOD1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eSuperoxide Dismutase, Cu-Zn (SOD1)\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: P08228\u003c\/p\u003e\u003ch2\u003eBiological role and pathway context\u003c\/h2\u003e\u003cp\u003eIn the literature, Superoxide Dismutase, Cu-Zn (SOD1) 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 Superoxide Dismutase, Cu-Zn (SOD1) 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\u003eSuperoxide Dismutase, Cu-Zn (SOD1) 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 Superoxide Dismutase, Cu-Zn (SOD1) 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\u003eSuperoxide Dismutase, Cu-Zn (SOD1)\u003c\/strong\u003e may also be referred to as \u003cstrong\u003eB430204E11Rik\u003c\/strong\u003e, \u003cstrong\u003eCu\/Zn-\u003c\/strong\u003e, and \u003cstrong\u003eCu\/Zn-SOD\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":52952728469869,"sku":"E2608Mo-96T","price":458.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/E2608Mo.jpg?v=1769147646"},{"product_id":"human-rna-binding-protein-fus-fus-tls-elisa-kit-bhe10504190","title":"Human RNA-binding protein FUS (FUS\/TLS) ELISA kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eRNA-binding protein FUS (FUS\/TLS)\u003c\/strong\u003e is a biological molecule commonly studied in signal transduction research. It is commonly used as a molecular readout in mechanistic and biomarker-focused studies.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P35637\u003c\/p\u003e\u003ch2\u003eBiological context\u003c\/h2\u003e\u003cp\u003eResearchers often monitor RNA-binding protein FUS (FUS\/TLS) in serum, plasma, and cell lysates to better understand themes such as mechanistic biology studies, biomarker-focused profiling, and disease-model research. 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 RNA-binding protein FUS (FUS\/TLS) may reflect differences in expression, secretion, turnover, or compartmentalization rather than a single mechanism. Interpretation is typically strengthened by evaluating related molecules (for example, complementary pathway markers and controls appropriate to the biological model) and by keeping pre-analytical variables consistent across groups.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003eIn publications and databases, RNA-binding protein FUS (FUS\/TLS) may also appear under names such as \u003cstrong\u003e75 kDa DNA pairing protein\u003c\/strong\u003e and \u003cstrong\u003e75 kDa DNA-pairing protein\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 RNA-binding protein FUS (FUS\/TLS) participates in.\u003c\/p\u003e","brand":"CUSABIO TECHNOLOGY LLC","offers":[{"title":"96 T","offer_id":52959589237101,"sku":"CSB-E17376h-96T","price":790.0,"currency_code":"USD","in_stock":true},{"title":"96 T×5","offer_id":52959589269869,"sku":"CSB-E17376h-96TX5","price":2765.0,"currency_code":"USD","in_stock":true},{"title":"96 T×10","offer_id":52959589302637,"sku":"CSB-E17376h-96TX10","price":5308.8,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/CSB-E17376h.png?v=1769247192"},{"product_id":"human-superoxide-dismutase-cu-zn-sod1-elisa-kit-bhe10504462","title":"Human Superoxide dismutase [Cu-Zn] (SOD1) ELISA kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eSuperoxide dismutase [Cu-Zn] (SOD1)\u003c\/strong\u003e is a biological molecule commonly studied in metabolism research. It is commonly used as a molecular readout in mechanistic and biomarker-focused studies.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P00441\u003c\/p\u003e\u003ch2\u003eBiological context\u003c\/h2\u003e\u003cp\u003eResearchers often monitor Superoxide dismutase [Cu-Zn] (SOD1) in serum, plasma, and tissue homogenates to better understand themes such as energy homeostasis, glucose and lipid metabolism, and insulin sensitivity and endocrine regulation. 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 Superoxide dismutase [Cu-Zn] (SOD1) may reflect differences in expression, secretion, turnover, or compartmentalization rather than a single mechanism. Interpretation is typically strengthened by evaluating related molecules (for example, insulin, adipokines, lipid-transport proteins, and stress-related enzymes) and by keeping pre-analytical variables consistent across groups.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003eIn publications and databases, Superoxide dismutase [Cu-Zn] (SOD1) may also appear under names such as \u003cstrong\u003eALS\u003c\/strong\u003e and \u003cstrong\u003eALS1\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 Superoxide dismutase [Cu-Zn] (SOD1) participates in.\u003c\/p\u003e","brand":"CUSABIO TECHNOLOGY LLC","offers":[{"title":"96 T","offer_id":52959602082157,"sku":"CSB-E16845h-96T","price":520.0,"currency_code":"USD","in_stock":true},{"title":"96 T×5","offer_id":52959602114925,"sku":"CSB-E16845h-96TX5","price":1820.0,"currency_code":"USD","in_stock":true},{"title":"96 T×10","offer_id":52959602147693,"sku":"CSB-E16845h-96TX10","price":3494.4,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/CSB-E16845h.png?v=1769247221"},{"product_id":"human-tar-dna-binding-protein-43-tardbp-tdp43-elisa-kit-bhe10504487","title":"Human TAR DNA-binding protein 43 (TARDBP\/TDP43) ELISA kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eTAR DNA-binding protein 43 (TARDBP\/TDP43)\u003c\/strong\u003e is a biological molecule commonly studied in others research. It is commonly used as a molecular readout in mechanistic and biomarker-focused studies.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q13148\u003c\/p\u003e\u003ch2\u003eBiological context\u003c\/h2\u003e\u003cp\u003eResearchers often monitor TAR DNA-binding protein 43 (TARDBP\/TDP43) in serum, plasma, cell culture supernates, and cerebrospinal fluid (CSF) to better understand themes such as mechanistic biology studies, biomarker-focused profiling, and disease-model research. 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 TAR DNA-binding protein 43 (TARDBP\/TDP43) may reflect differences in expression, secretion, turnover, or compartmentalization rather than a single mechanism. Interpretation is typically strengthened by evaluating related molecules (for example, complementary pathway markers and controls appropriate to the biological model) and by keeping pre-analytical variables consistent across groups.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003eIn publications and databases, TAR DNA-binding protein 43 (TARDBP\/TDP43) may also appear under names such as \u003cstrong\u003eALS10\u003c\/strong\u003e and \u003cstrong\u003eOTTHUMP00000002171\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 TAR DNA-binding protein 43 (TARDBP\/TDP43) participates in.\u003c\/p\u003e","brand":"CUSABIO TECHNOLOGY LLC","offers":[{"title":"96 T","offer_id":52959603065197,"sku":"CSB-E17007h-96T","price":615.0,"currency_code":"USD","in_stock":true},{"title":"96 T×5","offer_id":52959603097965,"sku":"CSB-E17007h-96TX5","price":2275.5,"currency_code":"USD","in_stock":true},{"title":"96 T×10","offer_id":52959603130733,"sku":"CSB-E17007h-96TX10","price":4368.98,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/CSB-E17007h.png?v=1769247223"},{"product_id":"human-uncharacterized-protein-c9orf72-c9orf72-elisa-kit-bhe10504794","title":"Human Uncharacterized protein C9orf72(C9orf72) ELISA kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003eUncharacterized protein C9orf72(C9orf72)\u003c\/strong\u003e is a biological molecule commonly studied in neuroscience research. It is commonly used as a molecular readout in mechanistic and biomarker-focused studies.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: Q96LT7\u003c\/p\u003e\u003ch2\u003eBiological context\u003c\/h2\u003e\u003cp\u003eResearchers often monitor Uncharacterized protein C9orf72(C9orf72) in serum, plasma, tissue homogenates, and cell lysates to better understand themes such as neuronal signaling and synaptic function, neuroinflammation, and neurodegeneration models. 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 Uncharacterized protein C9orf72(C9orf72) may reflect differences in expression, secretion, turnover, or compartmentalization rather than a single mechanism. Interpretation is typically strengthened by evaluating related molecules (for example, synaptic proteins, neurotrophic factors, and neuroinflammatory markers) and by keeping pre-analytical variables consistent across groups.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003eIn publications and databases, Uncharacterized protein C9orf72(C9orf72) may also appear under names such as \u003cstrong\u003eALSFTD\u003c\/strong\u003e and \u003cstrong\u003eC9orf72\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 Uncharacterized protein C9orf72(C9orf72) participates in.\u003c\/p\u003e","brand":"CUSABIO TECHNOLOGY LLC","offers":[{"title":"96 T","offer_id":52959617876333,"sku":"CSB-EL004345HU-96T","price":695.0,"currency_code":"USD","in_stock":true},{"title":"96 T×5","offer_id":52959617909101,"sku":"CSB-EL004345HU-96TX5","price":2571.5,"currency_code":"USD","in_stock":true},{"title":"96 T×10","offer_id":52959617941869,"sku":"CSB-EL004345HU-96TX10","price":4937.3,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/CSB-EL004345HU.png?v=1769247257"},{"product_id":"rat-superoxide-dismutase-1-soluble-sod1-elisa-kit-bhe10508675","title":"Rat superoxide dismutase 1, soluble (SOD1) ELISA kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003esuperoxide dismutase 1, soluble (SOD1)\u003c\/strong\u003e is a biological molecule commonly studied in metabolism research. It is commonly used as a molecular readout in mechanistic and biomarker-focused studies.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUniProt\u003c\/strong\u003e: P07632\u003c\/p\u003e\u003ch2\u003eBiological context\u003c\/h2\u003e\u003cp\u003eResearchers often monitor superoxide dismutase 1, soluble (SOD1) in serum, plasma, cell culture supernates, and tissue homogenates to better understand themes such as energy homeostasis, glucose and lipid metabolism, and insulin sensitivity and endocrine regulation. 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 superoxide dismutase 1, soluble (SOD1) may reflect differences in expression, secretion, turnover, or compartmentalization rather than a single mechanism. Interpretation is typically strengthened by evaluating related molecules (for example, insulin, adipokines, lipid-transport proteins, and stress-related enzymes) and by keeping pre-analytical variables consistent across groups.\u003c\/p\u003e\u003ch2\u003eNomenclature\u003c\/h2\u003e\u003cp\u003eIn publications and databases, superoxide dismutase 1, soluble (SOD1) may also appear under names such as \u003cstrong\u003eSod1\u003c\/strong\u003e and \u003cstrong\u003eSuperoxide dismutase [Cu-Zn]\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. 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The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human SQSTM1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human SQSTM1. 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 Human SQSTM1, 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 Human SQSTM1 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 OPTN. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse OPTN. 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 OPTN, 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 OPTN in the samples is then determined by comparing the OD of the samples to the standard curve.\u003c\/strong\u003e. After binding and washing, signal is converted to concentration using a standard curve.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eSample types\u003c\/strong\u003e: Tissue homogenates and other biological fluids.\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eDetection range\u003c\/strong\u003e: 0.16-10 ng\/mL\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eSensitivity\/LoD\u003c\/strong\u003e: 0.062 ng\/mL\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eAssay time\u003c\/strong\u003e: 3.5h\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"ELK Biotechnology","offers":[{"title":"96 T","offer_id":52965650137453,"sku":"ELK6110-96T","price":595.4,"currency_code":"USD","in_stock":true},{"title":"48 T","offer_id":52965650170221,"sku":"ELK6110-48T","price":416.0,"currency_code":"USD","in_stock":true},{"title":"96 T X 5","offer_id":52965650202989,"sku":"ELK6110-96TX5","price":2531.1,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/1h1qbq4v21p4717oo1b_ef920cf5-6f0c-483f-9a25-96b2df0218de.jpg?v=1771844576"},{"product_id":"mouse-fus-fusion-elisa-kit-bhe15206434","title":"Mouse FUS(Fusion) ELISA Kit","description":"\u003ch3\u003eScientific background\u003c\/h3\u003e\u003cp\u003e\u003cstrong\u003eFUS (Fusion)\u003c\/strong\u003e is a biologically relevant protein marker measured to support mechanistic studies and biomarker discovery (context dependent).\u003c\/p\u003e\u003cp\u003eProtein concentrations can change due to secretion, degradation, cell composition shifts, or post-transcriptional regulation, so ELISA readouts often add information beyond gene expression alone.\u003c\/p\u003e\u003cp\u003eQuantitative measurements help compare groups and time points using standardized curves and can be interpreted alongside phenotype and pathway-specific readouts.\u003c\/p\u003e\u003ch3\u003eWhy it matters\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eQuantify \u003cstrong\u003eFUS (Fusion)\u003c\/strong\u003e to compare biological changes across conditions, doses, or time points.\u003c\/li\u003e\n\u003cli\u003eGenerate concentration data from a standard curve to support biomarker and mechanistic studies.\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch3\u003eHow the ELISA works\u003c\/h3\u003e\u003cp\u003eDesigned for \u003cstrong\u003eMouse\u003c\/strong\u003e samples, this kit uses a \u003cstrong\u003eThe test principle applied in this kit is Sandwich enzyme immunoassay. 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The microtiter plate provided in this kit has been pre-coated with an antibody specific to Mouse SOD1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse SOD1. 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 SOD1, 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 SOD1 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 SOD1 relates to neuronal signaling and synaptic function, neuroinflammation, neurodegeneration models, and brain–body communication in neuroscience and metabolism research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in SOD1 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. 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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":52974772388205,"sku":"ERB0134-96T","price":650.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_23ee343d-bde6-4710-b590-0a396e09bd3c.jpg?v=1769596782"},{"product_id":"human-tdp43-tar-dna-binding-protein-43kda-elisa-kit-bhe10801534","title":"Human TDP43 (Tar DNA Binding Protein 43KDa) ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ehuman TDP43 (Tar DNA Binding Protein 43KDa)\u003c\/strong\u003e is a molecular target commonly studied in epigenetics, neuroscience, and metabolism research. 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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\u003eTDP43 (Tar DNA Binding Protein 43KDa)\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eTAR DNA-binding protein 43\u003c\/strong\u003e, \u003cstrong\u003eTDP-43\u003c\/strong\u003e, and \u003cstrong\u003eTARDBP\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 TDP43 relates to neuronal signaling and synaptic function, neuroinflammation, neurodegeneration models, and brain–body communication in epigenetics, neuroscience, and metabolism research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in TDP43 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\u003eTDP43 has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with epigenetics, neuroscience, and metabolism 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":52974800208237,"sku":"EH3862-96T","price":520.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_ff863f88-2d17-456d-b2cc-54d1dee178ec.jpg?v=1769597034"},{"product_id":"human-fus-rna-binding-protein-fus-elisa-kit-bhe10801785","title":"Human FUS (RNA-binding protein FUS) ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ehuman FUS (RNA-binding protein FUS)\u003c\/strong\u003e is a molecular target commonly studied in biomedical research. Regulatory proteins (including RNA-binding and transcription-associated factors) influence gene expression programs and cellular state transitions.\u003c\/p\u003e\u003ch2\u003eBiological role and mechanism\u003c\/h2\u003e\u003cp\u003eThe biological role of FUS 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 FUS 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\u003eFUS (RNA-binding protein FUS)\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eRNA-binding protein FUS\u003c\/strong\u003e, \u003cstrong\u003e75 kDa DNA-pairing protein\u003c\/strong\u003e, and \u003cstrong\u003eOncogene FUS\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 FUS relates to signal transduction, tissue homeostasis, stress responses, and disease-model biology in biomedical research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in FUS 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\u003eFUS 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":52974808039789,"sku":"EH14546-96T","price":520.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_07c0baab-d7d5-492f-8376-2dd0d2344f42.jpg?v=1769597119"},{"product_id":"mouse-tdp43-tar-dna-binding-protein-43-elisa-kit-bhe10802013","title":"Mouse TDP43 (TAR DNA Binding Protein 43) ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003emouse TDP43 (TAR DNA Binding Protein 43)\u003c\/strong\u003e is a molecular target commonly studied in epigenetics, neuroscience, and metabolism 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 TDP43 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 TDP43 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\u003eTDP43 (TAR DNA Binding Protein 43)\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eTAR DNA-binding protein 43\u003c\/strong\u003e, \u003cstrong\u003eTDP-43\u003c\/strong\u003e, and \u003cstrong\u003eTARDBP\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 TDP43 relates to neuronal signaling and synaptic function, neuroinflammation, neurodegeneration models, and brain–body communication in epigenetics, neuroscience, and metabolism research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in TDP43 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\u003eTDP43 has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with epigenetics, neuroscience, and metabolism 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":52974817935725,"sku":"EM1394-96T","price":520.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_ce2ba106-e6b3-4578-95f2-1927bc9e8990.jpg?v=1769597190"},{"product_id":"rat-sod1-superoxide-dismutase-cu-zn-elisa-kit-bhe10802940","title":"Rat SOD1 (Superoxide dismutase [Cu-Zn]) ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003erat SOD1 (Superoxide dismutase [Cu-Zn])\u003c\/strong\u003e is a molecular target commonly studied in neuroscience and metabolism 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 SOD1 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 SOD1 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\u003eSOD1 (Superoxide dismutase [Cu-Zn])\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eSuperoxide dismutase [Cu-Zn]\u003c\/strong\u003e, \u003cstrong\u003eSuperoxide dismutase 1\u003c\/strong\u003e, and \u003cstrong\u003ehSod1\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 SOD1 relates to neuronal signaling and synaptic function, neuroinflammation, neurodegeneration models, and brain–body communication in neuroscience and metabolism research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in SOD1 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\u003eSOD1 has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with neuroscience and metabolism 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":52974861517165,"sku":"ER0332-96T","price":455.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_0db6b8ad-7bcb-4eef-8054-3ebab0ddd5a3.jpg?v=1769597529"},{"product_id":"mouse-tbk1-serine-threonine-protein-kinase-tbk1-elisa-kit-bhe10803415","title":"Mouse Tbk1 (Serine\/threonine-protein kinase TBK1) ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003emouse Tbk1 (Serine\/threonine-protein kinase TBK1)\u003c\/strong\u003e is a molecular target commonly studied in immunology, signal transduction, and metabolism research. Enzymes contribute to cellular physiology through catalytic activity that supports metabolism, nucleic-acid processing, or signaling.\u003c\/p\u003e\u003ch2\u003eBiological role and mechanism\u003c\/h2\u003e\u003cp\u003eThe biological role of Tbk1 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 Tbk1 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\u003eTbk1 (Serine\/threonine-protein kinase TBK1)\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eSerine\/threonine-protein kinase TBK1\u003c\/strong\u003e, \u003cstrong\u003eNF-kappa-B-activating kinase\u003c\/strong\u003e, and \u003cstrong\u003eT2K\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 Tbk1 relates to innate and adaptive immune responses, cytokine signaling networks, host–pathogen interactions, and immune cell activation and trafficking in immunology, signal transduction, and metabolism research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in Tbk1 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\u003eTbk1 has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with immunology, signal transduction, and metabolism 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":52974885077357,"sku":"EM0580-96T","price":520.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_478807b0-2603-4612-a92f-c93d8c1428d9.jpg?v=1769597726"},{"product_id":"canine-sod1-elisa-kit-bhe10805919","title":"Canine SOD1 ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003ecanine SOD1\u003c\/strong\u003e is a molecular target commonly studied in neuroscience and metabolism 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 SOD1 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 SOD1 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\u003eSOD1\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eSuperoxide dismutase [Cu-Zn]\u003c\/strong\u003e, \u003cstrong\u003eSuperoxide dismutase 1\u003c\/strong\u003e, and \u003cstrong\u003ehSod1\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 SOD1 relates to neuronal signaling and synaptic function, neuroinflammation, neurodegeneration models, and brain–body communication in neuroscience and metabolism research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in SOD1 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\u003eSOD1 has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with neuroscience and metabolism 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":52975214985581,"sku":"ECA0067-96T","price":650.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_817842db-dd0f-45f7-a132-6ecbc12eacc9.jpg?v=1769598568"},{"product_id":"mouse-sod1-superoxide-dismutase-cu-zn-elisa-kit-bhe10806815","title":"Mouse SOD1 (Superoxide Dismutase [Cu-Zn]) ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003emouse SOD1 (Superoxide Dismutase [Cu-Zn])\u003c\/strong\u003e is a molecular target commonly studied in neuroscience and metabolism 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 SOD1 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 SOD1 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\u003eSOD1 (Superoxide Dismutase [Cu-Zn])\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eSuperoxide dismutase [Cu-Zn]\u003c\/strong\u003e, \u003cstrong\u003eSuperoxide dismutase 1\u003c\/strong\u003e, and \u003cstrong\u003ehSod1\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 SOD1 relates to neuronal signaling and synaptic function, neuroinflammation, neurodegeneration models, and brain–body communication in neuroscience and metabolism research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in SOD1 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\u003eSOD1 has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with neuroscience and metabolism 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":52975383445869,"sku":"EM0419-96T","price":455.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_2a56f65e-bdaf-43b9-8e46-b242b9153ca3.jpg?v=1769598842"},{"product_id":"chicken-sod1-superoxide-dismutase-cu-zn-elisa-kit-bhe10807106","title":"Chicken SOD1 (Superoxide dismutase [Cu-Zn]) ELISA Kit","description":"\u003ch2\u003eBackground\u003c\/h2\u003e\u003cp\u003e\u003cstrong\u003echicken SOD1 (Superoxide dismutase [Cu-Zn])\u003c\/strong\u003e is a molecular target commonly studied in neuroscience and metabolism 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 SOD1 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 SOD1 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\u003eSOD1 (Superoxide dismutase [Cu-Zn])\u003c\/strong\u003e may also be referenced as \u003cstrong\u003eSuperoxide dismutase [Cu-Zn]\u003c\/strong\u003e, \u003cstrong\u003eSuperoxide dismutase 1\u003c\/strong\u003e, and \u003cstrong\u003ehSod1\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 SOD1 relates to neuronal signaling and synaptic function, neuroinflammation, neurodegeneration models, and brain–body communication in neuroscience and metabolism research.\u003c\/li\u003e\n\u003cli\u003eInterpreting shifts in SOD1 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\u003eSOD1 has been investigated across diverse physiological and disease contexts, and changes in its abundance have been reported in areas aligned with neuroscience and metabolism 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":52975394161005,"sku":"ECH0113-96T","price":650.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/elisa_9f0723cd-848c-4dc7-9cb1-5f251ae299d9.jpg?v=1769598951"}],"url":"https:\/\/www.ebiohippo.com\/collections\/rs-tdp-43-fus-als-markers.oembed?page=8","provider":"BioHippo","version":"1.0","type":"link"}