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

This gene encodes the protein for complementation group A

KDa Mitochondrial Proteolipid

The encoded protein may function as a palmitoyltransferase

They may play a role in the immune system as well as in the central nervous system

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