CD141 Polyclonal Antibody, 50ul Nucleic Acid Isolation & Purification Mutations in MYOZ2 cause cardiomyopathy

Mutations in MYOZ2 cause cardiomyopathy familial hypertrophic type 16

The encoded protein may be involved in endocytic sorting

subunit:Binds to and is activated by YWHAZ when phosphorylated on Thr-182

serine and threonine metabolism and Lysine degradation

The La motif is also found in proteins unrelated to the La protein

CD141 Polyclonal Antibody, 50ul Nucleic Acid Isolation & Purification Mutations in MYOZ2 cause cardiomyopathyThe protein encoded by this intronless gene THBD (thrombomodulin) is an endothelial specific type I membrane receptor that binds thrombin. This binding results in the activation of protein C, which degrades clotting factors Va and VIIIa and reduces the amount of thrombin generated. Mutations in THBD are a cause of thromboembolic disease, also known as inherited thrombophilia.