FGF14, Polyclonal Antibody

bA397O8.2; FGF 14; FHF 4; FHF4; Fibroblast growth factor 14; Fibroblast growth factor homologous factor 4; mFHF-4(1B); MGC119129; MGC129318; MGC129319; RP11-397O8.6; SCA27

For Research Use Only. Not for use in diagnostic procedures.

Polyclonal

IgG

Rabbit

FGF14 antibody detects endogenous levels of total FGF14

The antiserum was purified by peptide affinity chromatography using SulfoLink Coupling Resin.

Liquid
Phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.

1mg/ml (lot specific)

Manufactured in an ISO 9001:2015 Certified Laboratory.

Manufactured in a lab with traceable raw materials manufactured on site. Coordinated product portfolio of antibodies, pairs, conjugates, recombinant proteins, and immunoassay materials available, please inquire.

Small volumes of anti-FGF14 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

Function: Probably involved in nervous system development and function.
Subunit Structure: Interacts with SCN8A (PubMed:26900580).
Similarity: Belongs to the heparin-binding growth factors family.

Western Blot (WB), ELISA (EIA)

WB: 1:500-1:2000

Western blot analysis of FGF14 expression in Mouse brain lysate (in RIPA buffer), The lane on the left is treated with the antigen-specific peptide.

Observed: 28 kDa
Predicted: 28 kDa

fibroblast growth factor 14

fibroblast growth factor 14

Fibroblast growth factor 14

FHF4; FGF-14; FHF-4  [Similar Products]

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, Jul 2008]

Probably involved in nervous system development and function.

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