ACAT-1 Polyclonal Antibody, 100ul Mini dry bath Mutations in this gene cause

Mutations in this gene cause cerebellar ataxia in humans

trisomic in derivative 22 syndrome and tetrasomic in cat-eye syndrome

Mutations and loss of expression of netrin suggest that variation in netrin may be involved in cancer development

that multiple polyadenylation sites are utilized in human to generate the 2 different sized mRNAs (5

expression of this intronless gene is significantly up-regulated in two cases of primary colon cancer

ACAT-1 Polyclonal Antibody, 100ul Mini dry bath Mutations in this gene causeACAT1 encodes a mitochondrially localized enzyme (acetyl CoA acetyltransferase 1) that catalyzes the reversible formation of acetoacetyl CoA from two molecules of acetyl CoA. Defects in ACAT1 are associated with 3 ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2 methyl 3 hydroxybutyric acid, 2 methylacetoacetic acid, tiglylglycine, and butanone.