FGF13 anticorps

N° du produit ABIN7263929

Détail du produit anti-FGF13 anticorps

Antigène: FGF13 (Fibroblast Growth Factor 13 (FGF13))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FGF13 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human FGF13 (NP_004105.1).

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000 IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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.

Détails sur FGF13

Antigène: FGF13 (Fibroblast Growth Factor 13 (FGF13))

Autre désignation: FGF13 (FGF13 Produits)

Synonymes: anticorps FGF13, anticorps fgf2, anticorps fhf2, anticorps fgf13, anticorps FGF-13, anticorps xFGF13, anticorps FGF2, anticorps FHF-2, anticorps FHF2, anticorps Fhf2, anticorps zgc:101784, anticorps fibroblast growth factor 13, anticorps fibroblast growth factor 13 L homeolog, anticorps fibroblast growth factor 13a, anticorps FGF13, anticorps fgf13, anticorps fgf13.L, anticorps Fgf13, anticorps fgf13a

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.

Poids moléculaire:

Observed_MW: 28 kDa

Calculated_MW: 21 kDa/22 kDa/25 kDa/27 kDa/28 kDa

ID gène: 2258

UniProt: Q92913

Pathways: Regulation of Cell Size