ACAT1 Antibody (YA1971)(PBS only)
(Synonyms: T2; MAT; ACAT; THIL)ACAT1 Antibody (YA1971) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to ACAT1.
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Host:
Rabbit
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Isotype:
IgG
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Application:
WB, IP
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Reactivity :
Human
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Formulation:
Supplied in PBS, pH 7.4.
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Conjugation:
Non-conjugated
Applications
| Application |
WB
WB: Western Blot
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IP
IP: Immunoprecipitation
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|---|---|---|
| Dilution Ratio | 1:500-1:1000 | 1:20 |
Product Details
ACAT1 Antibody (YA1971) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to ACAT1.
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Host Rabbit
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Species ReactivityHuman
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Observed Molecular WeightObserved band size: 45 kDaNote: Due to possible protein modifications or aggregation, the molecular weight should be confirmed by actual measurement, and the predicted value is for reference only.
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Calculated Molecular Weight Predicted band size: 45 kDa
A synthetic peptide of human ACAT1
Affinity Purified
Non-conjugated
IgG
Product Properties
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Appearance
Solution
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Formulation
Supplied in PBS, pH 7.4.
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Storage & Stability
Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.
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Shipping
Shipping with blue ice.
Background
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Function
ACAT1, also termed sterol O-acyltransferase 1 (SOAT1), is an endoplasmic reticulum-associated enzyme that catalyzes the conversion of free cholesterol and long-chain fatty acyl-CoA into cholesteryl esters, thereby maintaining intracellular cholesterol homeostasis and promoting lipid droplet formation[1][5]. Mechanistically, ACAT1-mediated cholesterol esterification limits excess free cholesterol accumulation and regulates cholesterol storage, linking membrane cholesterol balance to cellular metabolic adaptation[1][6]. In macrophages, increased cholesterol influx activates ACAT1 and drives cholesteryl ester deposition, a process closely associated with foam-cell formation and early atherosclerotic lesion development[7][2]. Experimental inhibition of ACAT activity enhances the pool of free cholesterol available for efflux and alters macrophage cholesterol metabolism, making ACAT1 a widely studied target in atherosclerosis models[7][2]. Beyond cardiovascular disease, dysregulated ACAT1-dependent cholesterol esterification has been reported in cancer and neurodegenerative disorders, where elevated cholesteryl ester accumulation is linked to altered cellular cholesterol handling[5][1][3]. Compared with the related isoform ACAT2/SOAT2, which is enriched in intestine and liver and participates in lipoprotein-associated cholesteryl ester production, ACAT1 is broadly expressed in peripheral tissues and is the dominant isoform involved in macrophage cholesterol storage and foam-cell biology[6][4]. For experimental applications, inhibitors including avasimibe and the ACAT1-selective compound K-604 have been used to investigate cholesterol esterification, plaque remodeling, and disease-associated lipid metabolic pathways[2][8].
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Subcellular Localization
Mitochondrion
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Isoforms & Post-Translational Modification
P24752 has 2 isomers: P24752-1: 45200 Da (predicted); P24752-2: 17175 Da (predicted).
Succinylation at Lys-268, adjacent to a coenzyme A binding site. Desuccinylated by SIRT5 (By similarity) -
Subunit
Homotetramer
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SwissProt ID
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Synonyms
T2; MAT; ACAT; THIL
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Research Field
Tags & Cell Markers
Documentation
References
[1]. Bhattacharjee P, et al. Targeting Sterol O-Acyltransferase/Acyl-CoA:Cholesterol Acyltransferase (ACAT): A Perspective on Small-Molecule Inhibitors and Their Therapeutic Potential. J Med Chem. 2022 Dec 22;65(24):16062-16098. [Content Brief]
[2]. Hai Q, et al. Acyl-Coenzyme A: Cholesterol Acyltransferase (ACAT) in Cholesterol Metabolism: From Its Discovery to Clinical Trials and the Genomics Era. Metabolites. 2021;11(8):543. [Content Brief]
[3]. Kiros M, et al. Trends in HIV-1 pretreatment drug resistance and HIV-1 variant dynamics among antiretroviral therapy-naive Ethiopians from 2003 to 2018: a pooled sequence analysis. Virol J. 2023 Oct 25;20(1):243. [Content Brief]
[8]. Bocan TM, et al. The ACAT inhibitor avasimibe reduces macrophages and matrix metalloproteinase expression in atherosclerotic lesions of hypercholesterolemic rabbits. Arterioscler Thromb Vasc Biol. 2000 Jan;20(1):70-9. [Content Brief]