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Also for FKTN (NM_001079802)
|Recombinant protein fragment contain a sequence corresponding to a region within amino acids 222 and 456 of Human FKTN|
|0.1M Tris, 0.1M Glycine, 10% Glycerol (pH7). 0.01% Thimerosal was added as a preservative.|
|Purified by antigen-affinity chromatography. (Protein A or G Sepharose)
|Homo sapiens fukutin (FKTN), transcript variant 1|
|CMD1X; FCMD; LGMD2M; MDDGA4; MDDGB4; MDDGC4|
|The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq]|
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A: H1299 B: Hela (anti-FKTN antibody diluted at 1:1000)
Immunofluorescence analysis of methanol-fixed HeLa, using Fukutin(anti-FKTN antibody) antibody at 1:200 dilution.