ELISA kits are commonly used to measure soluble biomarkers across a variety of research areas. ELISA kits for Human SOD1 can be quantified in various samples, including plasma, serum, supernatant, amniotic fluid, fetal umbilical vein blood.
Invitrogen ELISA kits exist in two...ELISA kits are commonly used to measure soluble biomarkers across a variety of research areas. ELISA kits for Human SOD1 can be quantified in various samples, including plasma, serum, supernatant, amniotic fluid, fetal umbilical vein blood.
Invitrogen ELISA kits exist in two formats: Uncoated and Coated....ELISA kits are commonly used to measure soluble biomarkers across a variety of research areas. ELISA kits for Human SOD1 can be quantified in various samples, including plasma, serum, supernatant, amniotic fluid, fetal umbilical vein blood.
Invitrogen ELISA kits exist in two formats: Uncoated and Coated. Uncoated ELISA kits include all the necessary reagents to coat your own plates and run your assay with maximum flexibility. Coated ELISA kits...
ELISA kits are commonly used to measure soluble biomarkers across a variety of research areas. ELISA kits for Human SOD1 can be quantified in various samples, including plasma, serum, supernatant, amniotic fluid, fetal umbilical vein blood.
Invitrogen ELISA kits exist in two formats: Uncoated and Coated. Uncoated ELISA kits include all the necessary reagents to coat your own plates and run your assay with maximum flexibility. Coated ELISA kits are ready-to-use and quality tested for sensitivity, specificity, precision and lot-to-lot consistency.
靶标信息
SOD1 (superoxide dismutase) binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body. This isozyme is a soluble cytoplasmic protein, acting as a homodimer to convert naturally-occuring but harmful superoxide radicals to molecular oxygen and hydrogen peroxide. The other isozyme is a mitochondrial protein. Mutations in this gene have been implicated as causes of familial amyotrophic lateral sclerosis. Rare transcript variants have been reported for this gene.