FGF13 antibody (AA 51-150) (Cy7)

Catalog No. ABIN734174

The Rabbit Polyclonal anti-FGF13 antibody has been validated for IF (cc) and IF (p). It is suitable to detect FGF13 in samples from Human.

Quick Overview for FGF13 antibody (AA 51-150) (Cy7) (ABIN734174)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FGF13 antibody is conjugated to Cy7

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

Product Details anti-FGF13 Antibody (Cy7)

Binding Specificity: AA 51-150

Predicted Reactivity: Human,Dog,Cow,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FGF13

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

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

Storage: -20 °C

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

Expiry Date: 12 months

Target Details for FGF13

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

Alternative Name: Fgf13

Background:

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.

Gene ID: 2258

Pathways: Regulation of Cell Size