PKC Alpha Polyclonal Antibody, 100ul[BT-AP07209] Vessels Mutations in this gene are

Mutations in this gene are known to be a cause of generalized thyroid hormone resistance (GTHR)

Targeting of numerous transmembrane proteins to the cell surface is thought to depend on their recognition by cargo receptors that interact with the adaptor machinery for anterograde traffic at the distal end of the Golgi complex

This gene encodes a DNA-dependent adenosine triphosphate (ATP)-metabolizing enzyme that functions as a 5' to 3' DNA helicase

Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN)

This protein also localizes to the nucleus and may affect cardiomyocyte differentiation after binding with the CSX/NKX2-5 transcription factor

PKC Alpha Polyclonal Antibody, 100ul[BT-AP07209] Vessels Mutations in this gene areProtein kinase C (PKC) is a family of serine and threonine specific protein kinases that can be activated by calcium and the second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC family members also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile