ELISA kits are commonly used to measure soluble biomarkers across a variety of research areas. ELISA kits for FGF23 are available for Human, Mouse and Rat which can be quantified in various samples, including plasma, serum, cell lysate, supernatant, tissue homogenate.
...ELISA kits are commonly used to measure soluble biomarkers across a variety of research areas. ELISA kits for FGF23 are available for Human, Mouse and Rat which can be quantified in various samples, including plasma, serum, cell lysate, supernatant, tissue homogenate.
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 FGF23 are available for Human, Mouse and Rat which can be quantified in various samples, including plasma, serum, cell lysate, supernatant, tissue homogenate.
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 FGF23 are available for Human, Mouse and Rat which can be quantified in various samples, including plasma, serum, cell lysate, supernatant, tissue homogenate.
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
The protein encoded by this gene is a member of the fibroblast growth factor family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. The product of this gene inhibits renal tubular phosphate transport. This gene was identified by its mutations associated with autosomal dominant hypophosphatemic rickets, an inherited phosphate wasting disorder. Abnormally high level expression of this gene was found in oncogenic hypophosphatemic osteomalacia, a phenotypically similar disease caused by abnormal phosphate metabolism. Mutations in this gene have also been shown to cause familial tumoral calcinosis with hyperphosphatemia.