ACAT-1 Polyclonal Antibody, 100ul Mini dry bath This gene encodes a member

This gene encodes a member of the steroid-thyroid hormone-retinoid receptor superfamily

LXN encodes the only known protein inhibitor of zinc-dependent metallocarboxypeptidases

Mutations in this gene cause cerebellar ataxia in humans

Plasmid vectors have been constructed utilizing the MBP domain that allow the synthesis of high levels of MBP-fusion proteins that can be purified in a one step procedure by affinity chromatography cross linked amylose resin

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

ACAT-1 Polyclonal Antibody, 100ul Mini dry bath This gene encodes a memberACAT1 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.