FGF13 antibody

Catalog No. ABIN2459900

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), ELISA

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FGF13.

Application Details

Application Notes: FGF13 antibody can be used for detection of FGF13 by ELISA at 1:62500. FGF13 antibody can be used for detection of FGF13 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Handling Advice: As with any antibody avoid repeat freeze-thaw cycles.

Storage: 4 °C/-20 °C

Storage Comment: For short periods of storage (days) store at 4 °C. For longer periods of storage, store FGF13 antibody at -20 °C.

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: FGF13 is probably involved in nervous system development and function.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 to a region associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a syndromal X-linked mental retardation, which suggests it may be a candidate gene for familial cases of the BFL syndrome. The function of this gene has not yet been determined. Two alternatively spliced transcripts encoding different isoforms have been described for this gene.

Molecular Weight: 27 kDa

Gene ID: 2258

NCBI Accession: NP_004105

UniProt: Q92913

Pathways: Regulation of Cell Size