GDC Rabbit Polyclonal Antibody, 20ul Recombinant Ab Production Mutations in TNNI3 cause familial

Mutations in TNNI3 cause familial hypertrophic cardiomyopathy type 7 (CMH7) and familial restrictive cardiomyopathy (RCM)

and regulation of cell volume

5-trisphosphate (PtdInsP3) and phosphatidic acid (PA) and acting in the regulation of the transport of vesicles from the endosomal recycling compartment (ERC) to the plasma membrane

transformation

The BRCA1-A complex possesses ubiquitinase activity and targets sites of double strand DNA breaks

GDC Rabbit Polyclonal Antibody, 20ul Recombinant Ab Production Mutations in TNNI3 cause familialThis gene encodes a protein that contains three tandemly repeated mitochondrial carrier protein domains. The encoded protein is localized in the inner membrane and facilitates the rapid transport and exchange of molecules between the cytosol and the mitochondrial matrix space. This gene has a possible role in Graves' disease.