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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
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$457.98
$538.80
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Quick Overview for FGF13 antibody (ABIN7244969)

Target

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

Reactivity

  • 88
  • 13
  • 12
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Rat, Mouse

Host

  • 50
  • 42
  • 1
Rabbit

Clonality

  • 54
  • 39
Polyclonal

Conjugate

  • 40
  • 8
  • 8
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 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

  • 56
  • 37
  • 34
  • 25
  • 15
  • 13
  • 13
  • 10
  • 4
  • 3
  • 2
  • 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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