FGF13 anticorps (AA 51-150) (Cy3)

N° du produit ABIN734171

L’anticorps Lapin Polyclonal anti-FGF13 a été validé pour IF (cc) et IF (p). Il convient pour détecter FGF13 dans des échantillons de Humain.

Aperçu rapide pour FGF13 anticorps (AA 51-150) (Cy3) (ABIN734171)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FGF13 est conjugé à/à la Cy3

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-FGF13 anticorps (Cy3)

Épitope: AA 51-150

Homologie: Human,Dog,Cow,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FGF13

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur FGF13

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

Autre désignation: Fgf13

Sujet:

Synonyms: Fibroblast Growth Factor-13, FGF 13, FGF 2, FGF-13, FGF2, FHF 2, FHF-2, FHF2, Fibroblast growth factor 13, Fibroblast growth factor homologous factor 2, OTTHUMP00000024143.

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. Fibroblast growth factor 13 (FGF13) is probably involved in nervous system development and function. Alternative splicing of this gene results in several transcript variants encoding different isoforms with different N-termini.

ID gène: 2258

Pathways: Regulation of Cell Size