FGF13 antibody

Catalog No. ABIN5697729

Product Details anti-FGF13 Antibody

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), Immunohistochemistry (IHC), ELISA

Immunogen: fibroblast growth factor 13

Isotype: IgG

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Comment:

Transfected HEK-293 cells were subjected to SDS PAGE followed by western blot with FNab03090( FGF13 Antibody) at dilution of 1:1000

Restrictions: For Research Use only

Handling

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

Preservative: Sodium azide

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

Handling Advice: Avoid repeated freeze / thaw cycles.

Storage: -20 °C

Expiry Date: 12 months

Target Details for FGF13

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

Alternative Name: FGF13 (FGF13 Products)

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

Background: Synonyms:FHF2 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.

Molecular Weight: 28-30 kDa

Gene ID: 2258

UniProt: Q92913

Pathways: Regulation of Cell Size