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

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

|online information:Estrogen receptor entry|polymorphism:Genetic variations in ESR1 are correlated with bone mineral density (BMD)

Association analysis shows preliminary evidence for the involvement of this gene in susceptibility to bipolar affective disorder and schizophrenia

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

|disease:Defects in ACAN are the cause of spondyloepiphyseal dysplasia type Kimberley (SEDK)

PKC Alpha Polyclonal Antibody, 100ul[BT-AP07209] Vessels Defects 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