GPT Rabbit Polyclonal Antibody, 100ul Live Cell Imaging Defects in ACAT1 are associated

Defects in ACAT1 are associated with 3-ketothiolase deficiency

The encoded protein may inhibit c-Jun N-terminal kinase (JNK) independently of CDC42 binding

It is a lectin that binds to sialylated glycoconjugates and mediates certain myelin-neuron cell-cell interactions

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

|Contains a central domain (substrate domain) containing multiple potential SH2-binding sites and a C-terminal domain containing a divergent helix-loop-helix (HLH) motif

GPT Rabbit Polyclonal Antibody, 100ul Live Cell Imaging Defects in ACAT1 are associatedThe 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.