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

FGF13 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN976829
  • 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)
    Sequence
    PKPLKVAMYK EPSLHDLTEF SRSGSGTPTK SRSVSGVLNG GKSMSHNEST
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-FGF13 Antibody(ARP55413_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
    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 in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked mental retardation mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini.

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

    Protein Interaction Partner: FGF13,SCN8A,MAPK8IP2

    Protein Size: 192
    Molecular Weight
    21 kDa
    Gene ID
    2258
    NCBI Accession
    NM_033642, NP_378668
    UniProt
    Q92913
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