CAN1 Polyclonal Antibody, 50ul Shaker&Mixing Defects in this gene are

Defects in this gene are a cause of xeroderma pigmentosum complementation group F (XP-F)

colorectal

Multiple alternatively spliced transcript variants have been found for this gene

and X-linked congenital idiopathic intestinal pseudoobstruction (CIIPX)

CAN1 Polyclonal Antibody, 50ul Shaker&Mixing Defects in this gene areThe calpains, calcium activated neutral proteases, are nonlysosomal, intracellular cysteine proteases. The mammalian calpains include ubiquitous, stomach specific, and muscle specific proteins. The ubiquitous enzymes consist of heterodimers with distinct large, catalytic subunits associated with a common small, regulatory subunit. This gene encodes the large subunit of the ubiquitous enzyme, calpain 1. Several transcript variants encoding two