CGB1 Polyclonal Antibody, 100ul Nucleic Acid Isolation & Purification Missense| nonsense| and frameshift mutations

Missense| nonsense| and frameshift mutations in this enzyme lead to ornithine transcarbamylase deficiency| which causes hyperammonemia

Chromosomal translocations have been characterized between this locus and the PAFAH1B3 (platelet-activating factor acetylhydrolase 1b

and a C-terminal extracellular region with four N-glycosylation sites

Interacts with SYCE1 and SYCE2

subcellular location:Present on the membrane of dendrites and cell bodies but excluded from axonal membrane

CGB1 Polyclonal Antibody, 100ul Nucleic Acid Isolation & Purification Missense| nonsense| and frameshift mutationsThe beta subunit of chorionic gonadotropin (CGB) is encoded by six highly homologous and structurally similar genes that are arranged in tandem and inverted pairs on chromosome 19q13. 3, and contiguous with the luteinizing hormone beta (LHB) subunit gene. The CGB genes are primarily distinguished by differences in the 5' untranscribed region. This gene was originally thought to be one of the two pseudogenes (CGB1 and CGB2) of CGB subunit, however,