FGF23 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00008074-T01

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Size:100 uL
Price: USD $ 247.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Western Blot
QC Test

Western Blot

Lane 1: FGF23 transfected lysate ( 28 KDa)
Lane 2: Non-transfected lysate.

SDS-PAGE Gel
QC Test

SDS-PAGE Gel

FGF23 transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-FGF23 full-length

    Host

    Human

    Theoretical MW (kDa)

    27.72

    Interspecies Antigen Sequence

    Mouse (71); Rat (72)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-FGF23 antibody (H00008074-B01) by Western Blots.

    Western Blot

    Lane 1: FGF23 transfected lysate ( 28 KDa)
    Lane 2: Non-transfected lysate.

    SDS-PAGE Gel

    FGF23 transfected lysate.

    Storage Buffer

    1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)

    Storage Instruction

    Store at -80°C. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot

  • Gene Info — FGF23

    Entrez GeneID

    8074

    GeneBank Accession#

    NM_020638

    Protein Accession#

    NP_065689

    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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