FGF14 antibody

Catalog No. ABIN7467601

The Rabbit Polyclonal anti-FGF14 antibody is suitable to detect FGF14 in samples from Human. It has been validated for WB, ICC and IF.

Quick Overview for FGF14 antibody (ABIN7467601)

Target: FGF14 (Fibroblast Growth Factor 14 (FGF14))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FGF14 antibody is un-conjugated

Application: Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)

Product Details anti-FGF14 Antibody

Cross-Reactivity: Human

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human FGF14. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: U87-MG , SK-N-SH , IMR32 , SK-N-AS

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 2.76 mg/mL

Buffer: 1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300

Preservative: ProClin

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

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for FGF14

Target: FGF14 (Fibroblast Growth Factor 14 (FGF14))

Alternative Name: fibroblast growth factor 14

Background: Fibroblast growth factor 14 , FGF-14 , FHF-4 , FHF4 , SCA27,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. A mutation in this gene is associated with autosomal dominant cerebral ataxia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq]

Molecular Weight: 28 kDa

Gene ID: 2259

UniProt: Q92915