Calpain 10 Polyclonal Antibody, 50ul Molecular Sciences Mutations in this gene that

Mutations in this gene that alter microtubule organization are associated with microcephaly and chorioretinopathy

which results in the activation of several signaling cascades

PKM encodes a protein involved in glycolysis

and may be involved in pancreatic lithogenesis

Mutations in this gene are associated with a Weill-Marchesani-like syndrome

Calpain 10 Polyclonal Antibody, 50ul Molecular Sciences Mutations in this gene thatCalpains represent a ubiquitous, well conserved family of calcium dependent cysteine proteases. The calpain proteins are heterodimers consisting of an invariant small subunit and variable large subunits. The large catalytic subunit has four domains: domain I, the N terminal regulatory domain that is processed upon calpain activation; domain II, the protease domain; domain III, a linker domain of unknown function; and domain IV, the calmodulin like