FGF23 monoclonal antibody, clone FG322-3

Catalog # MAB16059

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Price

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Quantity

Size:100 ug
Price: USD $ 638.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specification

    Product Description

    Mouse monoclonal antibody raised against recombinant human FGF23.

    Immunogen

    Recombinant protein corresponding to human FGF23.

    Host

    Mouse

    Reactivity

    Human

    Form

    Liquid

    Isotype

    IgG1, kappa

    Recommend Usage

    ELISA (1:2000-5000)
    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1:100-500)
    Western Blot (1:2000-5000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, pH 7.4.

    Storage Instruction

    For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

    Enzyme-linked Immunoabsorbent Assay

  • Gene Info — FGF23

    Entrez GeneID

    8074

    Protein Accession#

    Q9GZV9

    Gene Name

    FGF23

    Gene Alias

    ADHR, HPDR2, HYPF, PHPTC

    Gene Description

    fibroblast growth factor 23

    Omim ID

    193100 211900 605380

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. The product of this gene inhibits renal tubular phosphate transport. This gene was identified by its mutations associated with autosomal dominant hypophosphatemic rickets (ADHR), an inherited phosphate wasting disorder. Abnormally high level expression of this gene was found in oncogenic hypophosphatemic osteomalacia (OHO), a phenotypically similar disease caused by abnormal phosphate metabolism. Mutations in this gene have also been shown to cause familial tumoral calcinosis with hyperphosphatemia. [provided by RefSeq

    Other Designations

    tumor-derived hypophosphatemia inducing factor

  • Interactome
  • Pathway
  • Disease
  • Publication Reference
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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