FGF23 (Human) Recombinant Protein

Catalog # P8638

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Price

Stock

Quantity

Size:2 x 10 ug
Price: USD $ 428.00
Stock:
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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

    Human FGF23 recombinant protein with His tag in N-terminus expressed in Escherichia coli.

    Sequence

    MKHHHHHHASAEDDSERDPLNVLKPRARMTPAPASCSQELPSAEDNSPMASDPLGVVRGGRVNTHAGGTGPEGCRPFAKFI

    Host

    Escherichia coli

    Theoretical MW (kDa)

    8.67

    Form

    Lyophilized

    Preparation Method

    Escherichia coli expression system

    Purity

    > 90% as determined by SDS-PAGE.

    Storage Buffer

    Protein (0.5 mg/mL) was lyophilized from a solution containing 20 mM Tris, pH 7.5, 50 mM NaCl. Reconstitute the lyophilized powder in ddH2O to 0.5 mg/mL, and is not sterile! Please filter the product by an sterile filter before use.

    Storage Instruction

    Lyophilized protein should be stored at -20°C. Protein aliquots at 4°C for 2 weeks.
    Avoid repeated freeze/thaw cycles.

  • Applications

    SDS-PAGE

  • 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
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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