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FGF13 antibody

FGF13 Reactivity: Human, Rat, Mouse IHC, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7244969
  • Target See all FGF13 Antibodies
    FGF13 (Fibroblast Growth Factor 13 (FGF13))
    Reactivity
    • 73
    • 12
    • 11
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Rat, Mouse
    Host
    • 50
    • 31
    • 1
    Rabbit
    Clonality
    • 54
    • 28
    Polyclonal
    Conjugate
    • 36
    • 8
    • 8
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FGF13 antibody is un-conjugated
    Application
    • 55
    • 40
    • 22
    • 18
    • 17
    • 13
    • 13
    • 5
    • 5
    • 4
    • 3
    • 2
    • 1
    Immunohistochemistry (IHC), ELISA
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Synthetic peptide of human FGF13
    Isotype
    IgG
    Top Product
    Discover our top product FGF13 Primary Antibody
  • Application Notes
    IHC 1:40-1:200, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.26 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    FGF13 (Fibroblast Growth Factor 13 (FGF13))
    Alternative Name
    FGF13 (FGF13 Products)
    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.
    UniProt
    Q92913
    Pathways
    Regulation of Cell Size
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