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FGFA/FHFA (pan) Antibody: RPE

ORB150656
Biorbyt
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetFGF13
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Overview

  • Supplier
    Biorbyt
  • Product Name
    FGFA/FHFA (pan) antibody
  • Delivery Days Customer
    16
  • Application Supplier Note
    1 microg/ml of SMC-448 was sufficient for detection of FGFA/FHFA (pan) in 20 microg of rat brain lysate by colorimetric immunoblot analysis using Goat anti-mouse IgG:HRP as the secondary antibody.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
  • Applications Supplier
    WB (1:1000) ICC, IF, IHC, WB
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    N235/22 (Formerly sold as S235-22)
  • Concentration
    1 mg/ml
  • Conjugate
    RPE
  • Gene ID2258
  • Target name
    FGF13
  • Target description
    fibroblast growth factor 13
  • Target synonyms
    DEE90; FGF-13; FGF2; FHF2; FHF-2; fibroblast growth factor 13; fibroblast growth factor homologous factor 2; LINC00889
  • Host
    Mouse
  • Isotype
    IgG2b
  • Protein IDQ92913
  • Protein Name
    Fibroblast growth factor 13
  • Scientific Description
    Mouse monoclonal to FGFA (RPE). FGF13(Fibroblast growth factor 13), also called FHF2 is a protein that in humans is encoded by the FGF13 gene. The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF13is a large gene, extending over approximately 200 kb in Xq26. 3, and contains at least 7 exons. By cytogenetic, FISH, and database analysis, Gecz et al. (1999) localized the FGF13 gene within a 400-kb duplication interval on chromosome Xq26. 3. 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. This gene is located to a region associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a syndromal X-linked mental retardation, which suggests it may be a candidate gene for familial cases of the BFL syndrome. The function of this gene has not yet been determined. Two alternatively spliced transcripts encoding different isoforms have been described for this gene..
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    See Manual
  • UNSPSC
    12352203