兔抗FKTN多克隆抗体

Background:

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). Alternatively spliced transcript variants have been found for this gene.

Applications:

ELISA, WB

Name of antibody:

FKTN

Immunogen:

Synthetic peptide of human FKTN

Full name:

fukutin

Synonyms:

FCMD; CMD1X; LGMD2M; MDDGA4; MDDGB4; MDDGC4

SwissProt:

O75072

ELISA Recommended dilution:

5000-10000

WB Predicted band size:

54 kDa

WB Positive control:

Mouse liver tissue lysate

WB Recommended dilution:

500-2000