ARSH Polyclonal Antibody, 20ul Pipette Holder Specific mutations in DYSF have

Specific mutations in DYSF have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy

CSNK1A1 can phosphorylate a large number of proteins

The encoded protein may function as a palmitoyltransferase

relaxed finger rest

The protein encoded by this gene is a transcriptional coactivator that regulates the genes involved in energy metabolism

ARSH Polyclonal Antibody, 20ul Pipette Holder Specific mutations in DYSF haveSulfatases, such as ARSH, hydrolyze sulfate esters from sulfated steroids, carbohydrates, proteoglycans, and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling, and degradation of macromolecules (Sardiello et al., 2005