IP3R-I Polyclonal Antibody, 100ul[BT-AP04604] Primary Antibodies NBPF1 is a member of

NBPF1 is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1

and CC3 (CC for conserved cytoplasmic)

controlling transcriptional programs involved in lipid homeostasis and inflammation

Thus gene encodes the regulatory light chain associated with cardiac myosin beta (or slow) heavy chain

IP3R-I Polyclonal Antibody, 100ul[BT-AP04604] Primary Antibodies NBPF1 is a member ofITPR1 (inositol 1,4,5 trisphosphate receptor type 1) 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 ITPR1 cause spinocerebellar ataxia type 15, a disease associated with an heterogeneous group of cerebellar disorders. Multiple transcript variants have been identified for ITPR1.