CD55 Polyclonal Antibody, 50ul[BT-AP02092] Cell Screening and Imaging 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

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Human NCL gene consists of 14 exons with 13 introns and spans approximately 11kb

This gene encodes a protein which shares sequence similarity with other members of the type II chaperonin family

Belongs to the NPIP family

CD55 Polyclonal Antibody, 50ul[BT-AP02092] Cell Screening and Imaging Specific mutations in DYSF haveThe collagens are a superfamily of proteins that play a role in maintaining the integrity of various tissues. Collagens are extracellular matrix proteins and have a triple helical domain as their common structural element. Collagen VI is a major structural component of microfibrils. The basic structural unit of collagen VI is a heterotrimer of the alpha1(VI), alpha2(VI), and alpha3(VI) chains. The alpha2(VI) and alpha3(VI) chains are encoded by the