Troponin I-C Polyclonal Antibody, 100ul[BT-AP09225] Glassware Defects in SAR1B are a

Defects in SAR1B are a cause of chylomicron retention disease (CMRD)

Studies of a related mouse gene suggest that it functions in neurons

Defects in this gene have been associated with mitochondrial DNA depletion syndrome 10

HOXB4 is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain

Troponin I-C Polyclonal Antibody, 100ul[BT-AP09225] Glassware Defects in SAR1B are aTroponin I (TnI), along with troponin T (TnT) and troponin C (TnC), is one of 3 subunits that form the troponin complex of the thin filaments of striated muscle. TnI is the inhibitory subunit; blocking actin myosin interactions and thereby mediating striated muscle relaxation. The TnI subfamily contains three genes: tnI skeletal fast twitch, TnI skeletal slow twitch, and TnI cardiac. This gene encodes the TnI cardiac protein and is exclusively