WB result of ACAT2 Recombinant Rabbit mAb
Primary antibody: ACAT2 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: Hela whole cell lysate 25 μg
Lane 2: Hep G2 whole cell lysate 25 μg
Lane 3: MOLT-4 whole cell lysate 25 μg
Lane 4: Jurkat whole cell lysate 25 μg
Secondary antibody: Goat Anti-Rabbit IgG (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 41 kDa
Observed MW: 39 kDa
Product Details
Product Details
Product Specification
| Host | Rabbit |
| Antigen | ACAT2 |
| Location | Cytoplasm |
| Accession | Q9BWD1 |
| Antibody Type | Recombinant mAb |
| Isotype | IgG |
| Application | WB |
| Reactivity | Hu, Ms, Rt, Mk |
| Positive Sample | HeLa, HepG2, MOLT-4, Jurkat, mouse liver, mouse brain, mouse kidney, rat liver, rat brain, rat kidney, COS-7 |
| Purification | Protein A |
| Concentration | 0.5 mg/ml |
| Conjugation | Unconjugated |
| Physical Appearance | Liquid |
| Storage Buffer | PBS, 40% Glycerol, 0.05% BSA, 0.02% sodium azide |
| Stability & Storage | 12 months from date of receipt / reconstitution, -20 °C as supplied |
Dilution
| application | dilution | species |
| WB | 1:1000-1:5000 | Hu, Ms, Rt, Mk |
Background
ACAT2 (acyl-CoA:cholesterol acyltransferase 2) is a membrane-bound enzyme predominantly expressed in hepatocytes and intestinal mucosal cells. Unlike the broadly expressed ACAT1 isoenzyme, its function exhibits pronounced tissue specificity. The enzyme consists of 526 amino acids with a molecular weight of approximately 46 kDa, and its mRNA expression is coordinately regulated by the intestine-specific transcription factors Cdx2 and HNF1α. In normal hepatocytes, Cdx2 levels are extremely low, whereas elevated Cdx2 in hepatocellular carcinoma can lead to upregulated ACAT2 expression. Functionally, ACAT2 catalyzes the esterification of free cholesterol with long-chain acyl-CoA to generate cholesteryl esters, with its active site facing the endoplasmic reticulum lumen—in stark contrast to the cytosolic orientation of ACAT1. This unique topology determines that the primary physiological function of ACAT2 is to generate cholesteryl esters for the assembly and secretion of apolipoprotein B (apoB), participating in the absorption of dietary cholesterol in the intestine and providing the cholesteryl ester core for VLDL assembly in the liver. Gene knockout studies have confirmed that ACAT2-deficient mice show significantly restricted intestinal cholesterol absorption, markedly reduced cholesteryl ester content in hepatic and plasma lipoproteins, and are almost completely resistant to atherosclerosis in the ApoE-deficient background, establishing the critical role of ACAT2-derived cholesteryl esters in atherogenic lipoproteins. In addition, ACAT2 has been found to possess immunomodulatory functions in the tumor microenvironment, promoting M2-like polarization of tumor-associated macrophages to suppress CD8⁺ T cell activity, thereby driving tumor progression. Given its tissue distribution specificity and its central role in cholesterol absorption and the generation of atherogenic lipoproteins, ACAT2 has become an important target for drug development in the treatment of hypercholesterolemia and coronary heart disease.
Picture
Picture
Western Blot
WB result of ACAT2 Recombinant Rabbit mAb
Primary antibody: ACAT2 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: mouse liver lysate 25 μg
Lane 2: mouse brain lysate 25 μg
Lane 3: mouse kidney lysate 25 μg
Secondary antibody: Goat Anti-Rabbit IgG (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 41 kDa
Observed MW: 39 kDa
WB result of ACAT2 Recombinant Rabbit mAb
Primary antibody: ACAT2 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: rat liver lysate 25 μg
Lane 2: rat brain lysate 25 μg
Lane 3: rat kidney lysate 25 μg
Secondary antibody: Goat Anti-Rabbit IgG (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 41 kDa
Observed MW: 39 kDa
WB result of ACAT2 Recombinant Rabbit mAb
Primary antibody: ACAT2 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: COS-7 whole cell lysate 25 μg
Secondary antibody: Goat Anti-Rabbit IgG (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 41 kDa
Observed MW: 39 kDa
