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In summary, lipolytic enzyme ACOT8 is frequently upregulated in HCC (zeige FAM126A Proteine) clinical specimens. More importantly, ACOT8 silencing leads to inhibition of cell growth in HCC (zeige FAM126A Proteine) in vitro.
Acyl-CoA thioesterase 8 is a specific protein related to nodal metastasis and prognosis of lung adenocarcinoma.
ACOT4 (zeige ACOT4 Proteine) 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 (zeige SREBF2 Proteine) modulates brain palmitoyl-coa hydrolase gene transcription.
An isoform of long-chain acyl-CoA hydrolase (zeige ACOT1 Proteine) 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