IP3R-I Polyclonal Antibody, 50ul[BT-AP04604] ssDNA Synthesis Defects in PEX19 are a

Defects in PEX19 are a cause of Zellweger syndrome (ZWS)

|subunit:Part of the core histone deacetylase (HDAC) complex composed of HDAC1| HDAC2| RBBP4 and RBBP7

the MutS protein helps in the recognition of mismatched nucleotides prior to their repair

Engulfment and cell motility protein 1 interact with dedicator of cytokinesis proteins to promote phagocytosis and cell migration

contains seven transmembrane domains

IP3R-I Polyclonal Antibody, 50ul[BT-AP04604] ssDNA Synthesis Defects in PEX19 are aITPR1 (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.