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)

Alternatively spliced transcripts encoding different isoforms have been identified for SNCA

It is thought to be involved in the process of myelination

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

This gene may be associated with myelodysplastic syndrome

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