FGF13 antibody (AA 154-203)

Catalog No. ABIN1451931

The Rabbit Polyclonal anti-FGF13 antibody (ABIN1451931) specifically detects FGF13 in WB and ELISA. The antibody is reactive with Human, Rat and Mouse samples.

Quick Overview for FGF13 antibody (AA 154-203) (ABIN1451931)

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

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FGF13 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-FGF13 Antibody

Binding Specificity: AA 154-203

Purpose: FGF-13 Antibody

Specificity: FGF-13 Polyclonal Antibody detects endogenous levels of FGF-13 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: The antiserum was produced against synthesized peptide derived from human FGF13. AA range:154-203

Isotype: IgG

Application Details

Application Notes: WB 1:500 - 1:2000. ELISA: 1:5000. Not yet tested in other applications.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

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/1 year

Expiry Date: 12 months

Target Details for FGF13

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

Alternative Name: FGF13

Background:

Synonyms: FGF13; FHF2; Fibroblast growth factor 13; FGF-13; Fibroblast growth factor homologous factor 2; FHF-2

Background: The protein encoded byThis 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. [provided by RefSeq, Nov 2008],

Gene Name: FGF13

Protein Name: Fibroblast growth factor 13

Molecular Weight: 27 kDa

Gene ID: 2258

OMIM: 300070

UniProt: Q92913

Pathways: Regulation of Cell Size