PLCB1 Polyclonal Antibody, 100ul Centrifugal Filter Mutations in this gene have

Mutations in this gene have been associated with autosomal mental retardation-39 and autism spectrum disorder

Members of this family have identical structural organization that consists of an N-terminal coiled-coil motif

The members of this family share structural similarity

tumor necrosis factor receptor

Type XXI collagen is localized to tissues containing type I collagen and maintains the integrity of the extracellular matrix

PLCB1 Polyclonal Antibody, 100ul Centrifugal Filter Mutations in this gene haveThe protein encoded by this gene catalyzes the formation of inositol 1,4,5 trisphosphate and diacylglycerol from phosphatidylinositol 4,5 bisphosphate. This reaction uses calcium as a cofactor and plays an important role in the intracellular transduction of many extracellular signals. This gene is activated by two G protein alpha subunits, alpha q and alpha 11. Two transcript variants encoding different isoforms have been found for this gene.