IKKBeta Monoclonal Antibody, 50ul[BT-MCA0108] Lysosome Mutations in TNNI3 cause familial

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

Adducin binds with high affinity to Ca (2+)/calmodulin and is a substrate for protein kinases A and C

including venous thromboembolic disease

MEGF9 is suggested to participate in cell motility

skeletal muscle and kidney and

IKKBeta Monoclonal Antibody, 50ul[BT-MCA0108] Lysosome Mutations in TNNI3 cause familialThe protein encoded by this gene phosphorylates the inhibitor in the inhibitor NF kappa B complex, causing dissociation of the inhibitor and activation of NF kappa B. The encoded protein itself is found in a complex of proteins. Several transcript variants, some protein coding and some not, have been found for this gene.