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FGF23 antibody (AA 48-251)

FGF23 Reactivity: Mouse WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN4951022
  • Target See all FGF23 Antibodies
    FGF23 (Fibroblast Growth Factor 23 (FGF23))
    Binding Specificity
    • 15
    • 5
    • 5
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 48-251
    Reactivity
    • 58
    • 19
    • 14
    Mouse
    Host
    • 53
    • 23
    • 2
    Rabbit
    Clonality
    • 57
    • 21
    Polyclonal
    Conjugate
    • 41
    • 11
    • 6
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FGF23 antibody is un-conjugated
    Application
    • 42
    • 33
    • 17
    • 11
    • 9
    • 8
    • 6
    • 5
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Antigen affinity
    Immunogen
    Amino acids 48-251 of mouse FGF23 were used as the immunogen for the FGF23 antibody.
    Isotype
    IgG
    Top Product
    Discover our top product FGF23 Primary Antibody
  • Application Notes
    Optimal dilution of the FGF23 antibody should be determined by the researcher.\. Western blot: 0.1-0.5 μg/mL
    Restrictions
    For Research Use only
  • Buffer
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    Storage
    -20 °C
    Storage Comment
    After reconstitution, the FGF23 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target
    FGF23 (Fibroblast Growth Factor 23 (FGF23))
    Alternative Name
    FGF23 (FGF23 Products)
    Synonyms
    FGF23 antibody, ADHR antibody, FGFN antibody, HPDR2 antibody, HYPF antibody, PHPTC antibody, fibroblast growth factor 23 antibody, fgf23 antibody, FGF23 antibody, Fgf23 antibody
    Background
    Fibroblast growth factor 23 is a protein that in humans is encoded by the FGF23 gene. 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).
    UniProt
    Q9EPC2
    Pathways
    RTK Signaling, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway, Negative Regulation of Hormone Secretion
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