ABCA1 (ATP-binding cassette subfamily A member 1) is a transmembrane protein critical for cholesterol efflux and high-density lipoprotein (HDL) formation. ABCA1 Antibodies are tools used to study its role in lipid metabolism, atherosclerosis, and inflammation. These antibodies enable detection of ABCA1 in diverse experimental systems, including Western blot (WB), immunohistochemistry (IHC), immunoprecipitation (IP), and flow cytometry (FCM).
The following table summarizes key ABCA1 antibodies from commercial and academic sources:
Key Features:
Sensitivity: Detects endogenous ABCA1 in human and murine samples (e.g., liver, macrophages, neuroblastoma cells).
Specificity: Cross-reactivity with ABCA3/ABCA4/ABCA7 is excluded in select antibodies (e.g., Abcam’s [EPR27494-57]) .
Validation: Knockout (KO) cell lines and tissues confirm specificity (e.g., Abcam’s AB.H10) .
ABCA1’s biological roles are critical for cardiovascular and metabolic health:
ABCA1 facilitates the transfer of cholesterol and phospholipids to apolipoprotein A-I (apoA-I), forming nascent HDL particles . Defects in ABCA1 cause Tangier disease, characterized by low HDL and atherosclerosis .
ABCA1 modulates lipid rafts in macrophages, suppressing Toll-like receptor 4 (TLR4) signaling and inflammatory cytokine production . Mice lacking ABCA1 show heightened responses to lipopolysaccharides (LPS) .
In LDL receptor-deficient (LDLr⁻/⁻) mice with leukocyte-specific ABCA1 deletion, atherosclerotic lesions are larger, and macrophage infiltration increases . Plasma apoA-I levels are reduced, but HDL cholesterol remains unaffected .
HepG2 Cells: ABCA1 is detected at ~250–300 kDa, with induction by cholesterol or agonists like T0901317 .
Mouse Liver: A 254 kDa band is observed in wild-type but absent in ABCA1 knockout (KO) mice .
Pancreas: Exocrine glandular cells show strong ABCA1 staining, while islet cells exhibit weak positivity .
Lung Tissue: Antigen retrieval with TE buffer (pH 9.0) enhances detection .
KEGG: ath:AT5G61690
STRING: 3702.AT5G61690.1