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The protein encoded by ACAT1 belongs to the acyltransferase family. De plus, nous expédions ACAT1 Anticorps (184) et ACAT1 Protéines (15) et beaucoup plus de produits pour cette protéine.
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High ACAT1 expression is associated with breast cancer.
Insulin (Montrer INS Kits ELISA) promotes progression of colon cancer by upregulation of ACAT1.
ACAT1 exonic mutations that affect ESE sequences may result in aberrant splicing. This may affect the activity of mitochondrial acetoacetyl-CoA thiolase.
compound heterozygous of ACAT1 gene mutations probably underlie the beta-ketothiolase deficiency in our patient
Data indicate that acetyl-CoA (Montrer LPCAT2 Kits ELISA) acetyltransferase (ACAT1) and malate dehydrogenase (MDH2 (Montrer MDH Kits ELISA)) are involved in various drug-resistance-forming mechanisms.
ACAT1, ACACA (Montrer ACACA Kits ELISA), ALDH6A1 (Montrer ALDH6A1 Kits ELISA) and MTHFD1 (Montrer MTHFD1 Kits ELISA) represent novel biomarkers in adipose tissue associated with type 2 diabetes in obese individuals.
the pyruvate dehydrogenase (Montrer PDP Kits ELISA) complex is regulated by Tyr (Montrer TYR Kits ELISA) phosphorylation of PDP1 (Montrer PDP Kits ELISA), which toggles recruitment between ACAT1 and SIRT3 (Montrer SIRT3 Kits ELISA)
these findings indicate that ACAT1 expression could serve as a potential prognostic marker in prostate cancer, specifically in differentiating indolent and aggressive forms of cancer.
ACAT1 expression is substantially elevated in human castration-resistant metastatic prostate cancer tissues.
Data show that the ketone body metabolizing enzymes BDH1 (Montrer BDH1 Kits ELISA), BDH2 (Montrer BDH2 Kits ELISA), OXCT1 (Montrer OXCT1 Kits ELISA) and ACAT1 were expressed at the mRNA and protein level in all glioma cell lines.
Data show that microRNA miR (Montrer MLXIP Kits ELISA)-467b regulates the acetyl-CoA acetyltransferase 1 (ACAT1) expression via targeting ACAT1 (Montrer SOAT1 Kits ELISA) 3' untranslated regions (3'UTR (Montrer UTS2R Kits ELISA)).
In a mouse model, targeting ACAT1 (Montrer SOAT1 Kits ELISA) specifically in a myeloid lineage may benefit atherosclerosis progression by reducing the infiltration of foamy macrophages.
Oxidized low-density lipoprotein activated the TLR4 (Montrer TLR4 Kits ELISA)/MyD88 (Montrer MYD88 Kits ELISA)/NF-kappaB (Montrer NFKB1 Kits ELISA) inflammatory signaling pathway in vascular smooth muscle cell, which upregulates the ACAT1 (Montrer SOAT1 Kits ELISA) expression and promotes VSMC foam cell formation.
Exacerbation of liver fibrosis by ACAT1 (Montrer SOAT1 Kits ELISA) deficiency was dependent on free cholesterol accumulation-induced enhancement of TLR4 (Montrer TLR4 Kits ELISA) signaling.
ACAT1 (Montrer SOAT1 Kits ELISA) plays important roles in hematopoiesis in normal mouse and in Apoe (Montrer APOE Kits ELISA)(-/-) mouse during atherosclerosis development.
ApoA-I (Montrer APOA1 Kits ELISA) Helsinki promotes accumulation of ACAT1 (Montrer SOAT1 Kits ELISA) in a mouse macrophage cell line.
the plaque-modulating effects of K-604 can be explained by stimulation of procollagen production independent of ACAT (Montrer SOAT1 Kits ELISA) inhibition in addition to potent inhibition of macrophage ACAT-1 (Montrer SOAT1 Kits ELISA)
ACAT1 (Montrer SOAT1 Kits ELISA) gene ablation increases 24(S)-hydroxycholesterol content in the brain and ameliorates amyloid pathology in mice with Alzheimer disease.
ACAT1 displays less capacity than ACAT2 to differentiate cholesterol from sitosterol
ACAT1 (Montrer SOAT1 Kits ELISA) knockout macrophages show biochemical changes consistent with increased cytotoxicity and also a novel association with decreased expression of collagen type 3A1.
The transcript abundance of ACAT1 was increased in the more efficient low residual feed intake (RFI) animals and decreased in the less efficient high RFI animals
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.
acetoacetyl Coenzyme A thiolase
, acetoacetyl-CoA thiolase
, acetyl-CoA acetyltransferase, mitochondrial
, acetyl-Coenzyme A acetyltransferase 1
, mitochondrial acetoacetyl-CoA thiolase
, acetyl-Co A acetyltransferase 1 mitochondrial
, acetyl-coenzyme A acetyltransferase 1
, acetyl-Coenzyme A acetyltransferase 1 (acetoacetyl Coenzyme A thiolase)
, acetyl-CoA acetyltransferase 1
, Acetoacetyl-CoA thiolase A
, acetyl-CoA acetyltransferase A, mitochondrial