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- Tel: 858.663.9055
- Email: info@nsjbio.com
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Acetyl-CoA acetyltransferase, mitochondrial, also known as acetoacetyl-CoA thiolase, is an enzyme that in humans is encoded by the ACAT1 (Acetyl-Coenzyme A acetyltransferase 1) gene. 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.
Optimal dilution of the Acetyl-CoA acetyltransferase antibody should be determined by the researcher.
An E.coli-derived human recombinant protein (S10-Q404) was used as the immunogen for the Acetyl-CoA acetyltransferase antibody.
After reconstitution, the Acetyl-CoA acetyltransferase antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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