KPCD2 Polyclonal Antibody, 100ul Stepper leading to rapid and transient

leading to rapid and transient activation of numerous intracellular signaling pathways

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and macular dystrophy syndrome (EEMS)

Mutations in this gene are associated with retinal degenerative diseases including retinitis pigmentosa type 35 (RP35) and cone-rod dystrophy type 10 (CORD10)

through the regulatory roles of CDK4 and p53 in cell cycle G1 progression

KPCD2 Polyclonal Antibody, 100ul Stepper leading to rapid and transientThe protein encoded by this gene belongs to the protein kinase D (PKD) family of serine threonine protein kinases. This kinase can be activated by phorbol esters as well as by gastrin via the cholecystokinin B receptor (CCKBR) in gastric cancer cells. It can bind to diacylglycerol (DAG) in the trans Golgi network (TGN) and may regulate basolateral membrane protein exit from TGN. Alternative splicing results in multiple transcript variants encoding