GPT Rabbit Polyclonal Antibody, 100ul Live Cell Imaging Compared to other members of

Compared to other members of this family

The most abundant form of NF-kappa-B is NFKB1 complexed with the product of this gene

Defects in ACAT1 are associated with 3-ketothiolase deficiency

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

GPT Rabbit Polyclonal Antibody, 100ul Live Cell Imaging Compared to other members ofThe 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.