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FGF13 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement FGF13 dans IHC et ELISA. Il présente une réactivité envers Humain, Rat et Souris.
N° du produit ABIN7244969

Aperçu rapide pour FGF13 anticorps (ABIN7244969)

Antigène

Voir toutes FGF13 Anticorps
FGF13 (Fibroblast Growth Factor 13 (FGF13))

Reactivité

  • 78
  • 13
  • 11
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Rat, Souris

Hôte

  • 50
  • 34
  • 1
Lapin

Clonalité

  • 54
  • 31
Polyclonal

Conjugué

  • 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
Cet anticorp FGF13 est non-conjugé

Application

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

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Synthetic peptide of human FGF13

    Isotype

    IgG
  • Indications d'application

    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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    FGF13 (Fibroblast Growth Factor 13 (FGF13))

    Autre désignation

    FGF13

    Sujet

    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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