GPT Rabbit Polyclonal Antibody, 100ul Live Cell Imaging 2004 [PubMed 15175245])

2004 [PubMed 15175245])

NPR was determined to be a member of a distinct pentraxin protein subfamily

Compared to other members of this family

a developmental disorder caused by deletion of multiple genes at 7q11

and is further upregulated on neutrophil activation and during monocyte to macrophage differentiation

GPT Rabbit Polyclonal Antibody, 100ul Live Cell Imaging 2004 [PubMed 15175245])The protein encoded by this gene is an enzyme that catalyzes the first step in the dolichol linked oligosaccharide pathway for glycoprotein biosynthesis. This enzyme belongs to the glycosyltransferase family 4. This protein is an integral membrane protein of the endoplasmic reticulum. The congenital disorder of glycosylation type Ij is caused by mutation in the gene encoding this enzyme.