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IP3R-I Polyclonal Antibody, 100ul[BT-AP04604] Primary Antibodies APOBEC3A is a member of

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IP3R-I Polyclonal Antibody, 100ul[BT-AP04604] Primary Antibodies APOBEC3A 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.

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Description

APOBEC3A is a member of the cytidine deaminase gene family

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

C8 is a component of the complement system and contains three polypeptides

Among its related pathways are Alzheimer's disease and Respiratory electron transport

IP3R-I Polyclonal Antibody, 100ul[BT-AP04604] Primary Antibodies APOBEC3A 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.

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