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FGF23 anticorps (AA 48-251)

FGF23 Reactivité: Souris WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN4951022
  • Antigène Voir toutes FGF23 Anticorps
    FGF23 (Fibroblast Growth Factor 23 (FGF23))
    Épitope
    • 15
    • 5
    • 5
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 48-251
    Reactivité
    • 58
    • 19
    • 14
    Souris
    Hôte
    • 53
    • 23
    • 2
    Lapin
    Clonalité
    • 57
    • 21
    Polyclonal
    Conjugué
    • 41
    • 11
    • 6
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp FGF23 est non-conjugé
    Application
    • 42
    • 33
    • 17
    • 11
    • 9
    • 8
    • 6
    • 5
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Antigen affinity
    Immunogène
    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 Anticorps primaire
  • Indications d'application
    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
    Stock
    -20 °C
    Stockage commentaire
    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.
  • Antigène
    FGF23 (Fibroblast Growth Factor 23 (FGF23))
    Autre désignation
    FGF23 (FGF23 Produits)
    Synonymes
    anticorps FGF23, anticorps ADHR, anticorps FGFN, anticorps HPDR2, anticorps HYPF, anticorps PHPTC, anticorps fibroblast growth factor 23, anticorps fgf23, anticorps FGF23, anticorps Fgf23
    Sujet
    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
    Signalisation RTK, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway, Negative Regulation of Hormone Secretion
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