ACAT1 polyclonal, anti-human, mouse

Background:
This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene 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.

Synonyms: ACAT, MAT, T2, THIL

Cellular Location: Mitochondrion

Immunogen:
Recombinant protein of human ACAT1

Gene Symbol: ACAT1

Gene ID: 38

Swiss prot: P24752

Calculated MW: 45kDa

Recommended dilution:
WB 1:500-2000, IF 1:50-200,

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.