Anti-Human FGF23 Polyclonal Antibody

This gene encodes a member of the fibroblast growth factor family of proteins, which possess broad mitogenic and cell survival activities and are involved in a variety of biological processes. The product of this gene regulates phosphate homeostasis and transport in the kidney. The full-length, functional protein may be deactivated via cleavage into N-terminal and C-terminal chains. Mutation of this cleavage site causes autosomal dominant hypophosphatemic rickets (ADHR). Mutations in this gene are also associated with hyperphosphatemic familial tumoral calcinosis (HFTC).
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Properties

Data Sheet Click for Datasheet
Catalog Number PA06320
Size 100μl
Host Type Rabbit
Immunogen Synthesized peptide derived from the C-terminal region of human FGF-23.
Specificity Expressed in osteogenic cells particularly during phases of active bone remodeling. In adult trabecular bone, expressed in osteocytes and flattened bone-lining cells (inactive osteoblasts).
Isotype IgG
Reacitivity Human
Clone
Uniprot Q9GZV9
Concentration 1mg/mL
Dilution WB 1:500-1:2000, ELISA 1:20000
Formulation
Application WB,ELISA
Other Names ADHR,FGF-23,Fgf23,FGF23,FGFN,Fibroblast growth factor 23,Fibroblast growth factor 23 C-terminal peptide,Fibroblast growth factor 23 precursor,HPDR2,HYPF,Phosphatonin,PHPTC,Tumor derived hypophosphatemia inducing factor,Tumor-derived hypophosphatemia-inducing factor
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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