ACAT1

gene product
ACAT, THIL
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. [provided by RefSeq, Feb 2009]
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540 antibodies from 35 providers.

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AntibodyRefsTypeWBELICCIPIHCFC
Atlas Antibodies
2 antibodies
Novus Biologicals
20 antibodies
GeneTex
8 antibodies
NovoPro Bioscience Inc.
11 antibodies
Proteintech Group
1 antibody
Acris Antibodies GmbH
13 antibodies
antibodies-online
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Biorbyt
28 antibodies
OriGene
14 antibodies
Abnova Corporation
12 antibodies
LifeSpan BioSciences, Inc.
57 antibodies
Invitrogen Antibodies
6 antibodies
Antibodies.com
4 antibodies
Aviva Systems Biology
7 antibodies
Bioworld Technology, Inc
2 antibodies
NSJ Bioreagents
3 antibodies
Affinity Biosciences
1 antibody
Arigo
4 antibodies
Abgent
8 antibodies
St John's Laboratory
7 antibodies
Everest Biotech
2 antibodies
ProSci
8 antibodies
Boster Biological Technology
1 antibody
Cell Signaling Technology, Inc
1 antibody
Abbkine Scientific Co.Ltd.
1 antibody
Creative Biolabs
9 antibodies
United States Biological
66 antibodies
MyBioSource
9 antibodies
RayBiotech, Inc.
6 antibodies
RabMAbs
2 antibodies
Creative Diagnostics
5 antibodies
Sigma-Aldrich
3 antibodies
Abbexa
3 antibodies
GenWay
1 antibody