CK096 Rabbit Polyclonal Antibody, 50ul Cell Function Analysis Mutations in this gene have

Mutations in this gene have been associated with disruption of the retinal pigment epithelium (RPE) phagocytosis pathway and onset of autosomal recessive retinitis pigmentosa (RP)

This isoform requires magnesium for its function and cleaves specific sites in A+U-rich regions of RNA

Reduced expression of this gene resulted in DNA replication defects| consistent with the demonstrated role for this gene in Simian Virus 40 (SV40) viral replication

This gene encodes a member of the carbohydrate kinase PfkB family

and couples to Gs thus stimulating adenylate cyclase

CK096 Rabbit Polyclonal Antibody, 50ul Cell Function Analysis Mutations in this gene have