IP3R-I(Phospho Ser1764) Polyclonal Antibody, 20ul Peptide Modification including cysteine- and serine- rich

including cysteine- and serine- rich regions

The encoded protein is described as a hexacoordinate hemoglobin which binds ligand differently from the pentacoordinate hemoglobins involved in oxygen transport

This gene previously was referred to as NEDD6 (neural precursor cell expressed

Mutation of this cleavage site causes autosomal dominant hypophosphatemic rickets (ADHR)

They are expressed in single layer epithelial tissues of the body

IP3R-I(Phospho Ser1764) Polyclonal Antibody, 20ul Peptide Modification including cysteine- and serine- richThis gene encodes an intracellular receptor for inositol 1,4,5 trisphosphate. Upon stimulation by inositol 1,4,5 trisphosphate, this receptor mediates calcium release from the endoplasmic reticulum. Mutations in this gene cause spinocerebellar ataxia type 15, a disease associated with an heterogeneous group of cerebellar disorders. Multiple transcript variants have been identified for this gene.