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In summary, lipolytic enzyme ACOT8 is frequently upregulated in HCC clinical specimens. More importantly, ACOT8 silencing leads to inhibition of cell growth in HCC in vitro.
Acyl-CoA thioesterase 8 is a specific protein related to nodal metastasis and prognosis of lung adenocarcinoma.
ACOT4 and ACOT8 are responsible for the termination of beta-oxidation of dicarboxylic acids of medium-chain length with the concomitant release of the corresponding free acids
SREBP2 modulates brain palmitoyl-coa hydrolase gene transcription.
An isoform of long-chain acyl-CoA hydrolase may be responsible for the nafamostat hydrolysis in human liver cytosol.
The protein encoded by this gene is a peroxisomal thioesterase that appears to be involved more in the oxidation of fatty acids rather than in their formation. The encoded protein can bind to the human immunodeficiency virus-1 protein Nef, and mediate Nef-induced down-regulation of CD4 in T-cells.
peroxisomal acyl-CoA thioesterase
, acyl-coenzyme A thioesterase 8
, peroxisomal acyl-CoA thioesterase 1
, acyl-CoA thioesterase 8
, HIV-Nef associated acyl-CoA thioesterase
, choloyl-CoA hydrolase
, choloyl-coenzyme A thioesterase
, long-chain fatty-acyl-CoA hydrolase
, palmitoyl-CoA hydrolase
, peroxisomal acyl-coenzyme A thioester hydrolase 1
, peroxisomal long-chain acyl-CoA thioesterase 1
, thioesterase II
, thioesterase III
, peroxisomal acyl-CoA thioesterase 2
, 4,8-dimethylnonanoyl-CoA thioesterase
, 48-dimethylnonanoyl-CoA thioesterase