Mouse Glia-derived Nexin, SERPINE2 ELISA Kit, 96T Purification 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

Belongs to the CLASP family

subcellular location:Upon EGF stimulation

The protein encoded by SDC4 (syndecan 4) is a transmembrane (type I) heparan sulfate proteoglycan that functions as a receptor in intracellular signaling

This type II cytokeratin is specifically expressed in differentiated layers of the mucosal and esophageal epithelia with family member KRT13

Mouse Glia-derived Nexin, SERPINE2 ELISA Kit, 96T Purification Specific mutations in DYSF haveSerine protease inhibitor with activity toward thrombin, trypsin, and urokinase. Promotes neurite extension by inhibiting thrombin. Binds heparin.