ARG66889

anti-FGF23 antibody

anti-FGF23 antibody for ICC/IF,Western blot and Human

Overview

Product Description Rabbit Polyclonal antibody recognizes FGF23
Tested Reactivity Hu
Tested Application ICC/IF, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name FGF23
Antigen Species Human
Immunogen Synthetic peptide within aa. 151-200 of Human FGF23.
Conjugation Un-conjugated
Alternate Names ADHR; Phosphatonin; HPDR2; FGFN; Tumor-derived hypophosphatemia-inducing factor; PHPTC; FGF-23; Fibroblast growth factor 23; HYPF

Application Instructions

Application Suggestion
Tested Application Dilution
ICC/IF1:200 - 1:1000
WB1:500 - 1:2000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control Jurkat
Observed Size ~ 28 kDa

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer PBS, 0.02% Sodium azide, 50% Glycerol and 0.5% BSA.
Preservative 0.02% Sodium azide
Stabilizer 50% Glycerol and 0.5% BSA
Concentration 1 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 8074 Human FGF23

Swiss-port # Q9GZV9 Human Fibroblast growth factor 23

Gene Symbol FGF23
Gene Full Name fibroblast growth factor 23
Background 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). [provided by RefSeq, Feb 2013]
Function Regulator of phosphate homeostasis. Inhibits renal tubular phosphate transport by reducing SLC34A1 levels. Upregulates EGR1 expression in the presence of KL (By similarity). Acts directly on the parathyroid to decrease PTH secretion (By similarity). Regulator of vitamin-D metabolism. Negatively regulates osteoblast differentiation and matrix mineralization. [UniProt]
Cellular Localization Secreted. Note=Secretion is dependent on O-glycosylation. [UniProt]
Calculated MW 28 kDa
PTM Following secretion this protein is inactivated by cleavage into a N-terminal fragment and a C-terminal fragment. The processing is effected by proprotein convertases.

O-glycosylated by GALT3. Glycosylation is necessary for secretion; it blocks processing by proprotein convertases when the O-glycan is alpha 2,6-sialylated. Competition between proprotein convertase cleavage and block of cleavage by O-glycosylation determines the level of secreted active FGF23. [UniProt]

Images (2) Click the Picture to Zoom In

  • ARG66889 anti-FGF23 antibody ICC/IF image

    Immunofluorescence: HUVEC cells stained with ARG66889 anti-FGF23 antibody. The picture on the right is blocked with the synthetic peptide.

  • ARG66889 anti-FGF23 antibody WB image

    Western blot: Jurkat cell lysate stained with ARG66889 anti-FGF23 antibody at 1:1000 dilution, overnight at 4°C.