FGF23 (Human) ELISA Kit

Catalog # KA5418

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Size:1 Kit
Price: USD $ 648.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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QC Test

The standard curve is for the purpose of illustration only and should not be used to calculate unknowns. A standard curve should be generated each time the assay is performed.

  • Specification

    Product Description

    FGF23 (Human) ELISA Kit is a sandwich enzyme-linked immunosorbent assay for quantitative detection of human FGF23 in serum, plasma, tissue homogenates, cell lysates, cell culture supernatants and other biological fluids.

    Suitable Sample

    Serum, plasma, tissue homogenates, cell lysates, cell culture supernatants and other biological fluids

    Sample Volume

    100 uL

    Label

    HRP-conjugated

    Detection Method

    Colorimetric

    Assay Type

    Quantitative

    Calibration Range

    15.625 to 1000 pg/mL

    Reactivity

    Human

    Regulatory Status

    For research use only (RUO)

    Quality Control Testing

    Standard curve

    The standard curve is for the purpose of illustration only and should not be used to calculate unknowns. A standard curve should be generated each time the assay is performed.

    Storage Instruction

    Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

  • Applications

    Quantification

  • Gene Info — FGF23

    Entrez GeneID

    8074

    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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