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Fibroblast Growth Factor 13 (FGF13) (Middle Region) Peptide

FGF13 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN976828
  • Target See all FGF13 products
    FGF13 (Fibroblast Growth Factor 13 (FGF13))
    Protein Region
    Middle Region
    Origin
    Human
    Source
    • 9
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-FGF13 antibody (Catalog #: ARP55412_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    Purification
    Purified
  • Application Notes
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    FGF13 (Fibroblast Growth Factor 13 (FGF13))
    Synonyms
    FGF13 Peptide, fgf2 Peptide, fhf2 Peptide, fgf13 Peptide, FGF-13 Peptide, xFGF13 Peptide, FGF2 Peptide, FHF-2 Peptide, FHF2 Peptide, Fhf2 Peptide, zgc:101784 Peptide, fibroblast growth factor 13 Peptide, fibroblast growth factor 13 L homeolog Peptide, fibroblast growth factor 13a Peptide, FGF13 Peptide, fgf13 Peptide, fgf13.L Peptide, Fgf13 Peptide, fgf13a Peptide
    Background
    FGF13 is probably involved in nervous system development and function.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. 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.

    Alias Symbols: FGF2, FHF2, FHF-2, FGF-13

    Protein Interaction Partner: FGF13,SCN8A,MAPK8IP2

    Protein Size: 245
    Molecular Weight
    27 kDa
    Gene ID
    2258
    NCBI Accession
    NM_004114, NP_004105
    UniProt
    Q92913
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