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FGF13 antibody

This Rabbit Polyclonal antibody specifically detects FGF13 in IHC and ELISA. It exhibits reactivity toward Human, Rat and Mouse.
Catalog No. ABIN7244969

Quick Overview for FGF13 antibody (ABIN7244969)

Target

See all FGF13 Antibodies
FGF13 (Fibroblast Growth Factor 13 (FGF13))

Reactivity

  • 78
  • 13
  • 11
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Rat, Mouse

Host

  • 50
  • 34
  • 1
Rabbit

Clonality

  • 54
  • 31
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
  • 1
  • 1
  • 1
This FGF13 antibody is un-conjugated

Application

  • 55
  • 39
  • 28
  • 21
  • 15
  • 13
  • 13
  • 11
  • 4
  • 3
  • 2
  • 1
  • 1
Immunohistochemistry (IHC), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Synthetic peptide of human FGF13

    Isotype

    IgG
  • 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

    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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