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FGF23 Protein (AA 1-251) (His tag)

FGF23 Origin: Human Host: HEK-293 Cells Recombinant >90 % (SDS-PAGE) SDS Active
Catalog No. ABIN5564312
  • Target See all FGF23 Proteins
    FGF23 (Fibroblast Growth Factor 23 (FGF23))
    Protein Type
    Recombinant
    Biological Activity
    Active
    Protein Characteristics
    AA 1-251
    Origin
    • 19
    • 3
    • 3
    • 1
    Human
    Source
    • 13
    • 4
    • 4
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This FGF23 protein is labelled with His tag.
    Application
    SDS-PAGE (SDS)
    Cross-Reactivity
    Human
    Characteristics
    Signal peptide and human FGF-23 (aa 1-251) are fused at the C-terminus to a His-tag.
    Purity
    >90 % (SDS-PAGE)
    Endotoxin Level
    <0.01EU/μg purified protein (LAL test, Lonza).
    Top Product
    Discover our top product FGF23 Protein
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Comment

    Activates ERK and FRS2alpha phosphorylation in Klotho expressing cells.

    Restrictions
    For Research Use only
  • Format
    Solid
    Concentration
    Lot specific
    Buffer
    Lyophilized. Contains PBS.
    Storage
    4 °C,-20 °C
    Storage Comment
    Short Term Storage: +4°C
    Long Term Storage: -20°C
    Stable for at least 6 months after receipt when stored at -20°C. Working aliquots are stable for up to 3 months when stored at -20°C.
    Expiry Date
    6 months
  • Target
    FGF23 (Fibroblast Growth Factor 23 (FGF23))
    Alternative Name
    FGF-23 (FGF23 Products)
    Synonyms
    FGF23 Protein, ADHR Protein, FGFN Protein, HPDR2 Protein, HYPF Protein, PHPTC Protein, fibroblast growth factor 23 Protein, fgf23 Protein, FGF23 Protein, Fgf23 Protein
    Background
    FGF-23 (Fibroblast growth factor 23) is a regulator of phosphate homeostasis. It upregulates EGR1 expression in the presence of KLBy. Acts directly on the parathyroid to decrease PTH secretion. Regulates the vitamin-D metabolism. Negatively regulates osteoblast differentiation and matrix mineralization. Defects in FGF-23 are the cause of autosomal dominant hypophosphataemic rickets (ADHR) and of hyperphosphatemic familial tumoral calcinosis (HFTC).
    Molecular Weight
    ~30kDa (SDS-PAGE, full-length). FGF23 is cleaved between Arg179 and Ser180 (two bands of ~14kDa and ~16kDa).
    UniProt
    Q9GZV9
    Pathways
    RTK Signaling, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway, Negative Regulation of Hormone Secretion
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