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- Tel: 858.663.9055
- Email: info@nsjbio.com
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Acetyl-CoA acetyltransferase 1 is a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in the gene encoding ACAT1 are associated with the alpha-methylacetoaceticaciduria disorder,an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone.
Titration of the ACAT1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.
A portion of amino acids 296-329 from the human protein was used as the immunogen for this ACAT1 antibody.
Aliquot the ACAT1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
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