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

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

SKU: 74447293215

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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.

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Description

Mutations in MYOZ2 cause cardiomyopathy familial hypertrophic type 16

HLA-DQB2 belongs to the family of HLA class II beta chain paralogs

serine and threonine metabolism and Lysine degradation

developmental stage:Expressed throughout the cell cycle

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.

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