IRK8 Polyclonal Antibody, 20ul Immunoassays Defects in ACTC1 have been

Defects in ACTC1 have been associated with idiopathic dilated cardiomyopathy (IDC) and familial hypertrophic cardiomyopathy (FHC)

and may also have a role in immune tolerance at the maternal-fetal interface

Alternate splicing results in multiple transcript variants encoding different isoforms

The eNoSC complex is able to sense the energy status of cell: upon glucose starvation

IRK8 Polyclonal Antibody, 20ul Immunoassays Defects in ACTC1 have beenPotassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G proteins. Defects in this gene may be a cause of J wave syndromes and sudden infant death