Use your antibodies-online credentials, if available.
抗Human ABCA1 抗体:
抗Rat (Rattus) ABCA1 抗体:
抗Mouse (Murine) ABCA1 抗体:
Chicken Polyclonal ABCA1 Primary Antibody for ChIP, ELISA - ABIN152883
Krimbou, Denis, Haidar, Carrier, Marcil, Genest: Molecular interactions between apoE and ABCA1: impact on apoE lipidation. in Journal of lipid research 2004
Show all 253 Pubmed References
Chicken Polyclonal ABCA1 Primary Antibody for ELISA, ICC - ABIN268847
Burgess, Kiss, Zheng, Zachariah, Marcel: Trypsin-sensitive and lipid-containing sites of the macrophage extracellular matrix bind apolipoprotein A-I and participate in ABCA1-dependent cholesterol efflux. in The Journal of biological chemistry 2002
Show all 13 Pubmed References
Chicken Polyclonal ABCA1 Primary Antibody for ELISA, IHC (fro) - ABIN268848
Murthy, Born, Mathur, Field: LXR/RXR activation enhances basolateral efflux of cholesterol in CaCo-2 cells. in Journal of lipid research 2002
Show all 13 Pubmed References
Mouse (Murine) Monoclonal ABCA1 Primary Antibody for IHC (p), WB - ABIN268899
Zhou, Choi, Li, Xu, Herz: LRP1 controls cPLA2 phosphorylation, ABCA1 expression and cellular cholesterol export. in PLoS ONE 2009
Show all 6 Pubmed References
Human Monoclonal ABCA1 Primary Antibody for CyTOF, FACS - ABIN4277133
Wang, Zhang, Chou, Liang, Gu, Ma: Cyclosporine stimulates the renal epithelial sodium channel by elevating cholesterol. in American journal of physiology. Renal physiology 2009
Show all 5 Pubmed References
Human Polyclonal ABCA1 Primary Antibody for WB - ABIN3043773
Shang, Yu, Wang, Chen, Fang, Yang, Zhou, Nie, Zhou, Zhou: Fibroblast growth factor 21 enhances cholesterol efflux in THP-1 macrophage-derived foam cells. in Molecular medicine reports 2014
Show all 5 Pubmed References
Human Polyclonal ABCA1 Primary Antibody for WB - ABIN3044206
Chen: Effects of Chinese Herbal Compound "Xuemai Ning"on Rabbit Atherosclerosis Model and Expression of ABCA1. in International journal of biomedical science : IJBS 2013
Show all 5 Pubmed References
Cow (Bovine) Polyclonal ABCA1 Primary Antibody for WB - ABIN2781512
Fu, Mukhamedova, Ip, DSouza, Henley, DiTommaso, Kesani, Ditiatkovski, Jones, Lane, Jennings, Smyth, Kile, Sviridov: ABCA12 regulates ABCA1-dependent cholesterol efflux from macrophages and the development of atherosclerosis. in Cell metabolism 2013
Chicken Polyclonal ABCA1 Primary Antibody for ELISA, FACS - ABIN446266
Ingram, Crowther, Little, Freeman, Harliwong, Veleva, Hassall, Remke, Taylor, Hallahan: ABC transporter activity linked to radiation resistance and molecular subtype in pediatric medulloblastoma. in Experimental hematology & oncology 2013
Mouse (Murine) Monoclonal ABCA1 Primary Antibody for FACS, IF - ABIN2477218
Zarubica, Trompier, Chimini: ABCA1, from pathology to membrane function. in Pflügers Archiv : European journal of physiology 2007
identified HuR (显示 ELAVL1 抗体) as a novel posttranscriptional regulator of ABCA1 expression and cellular cholesterol homeostasis, thereby opening new avenues for increasing cholesterol efflux from atherosclerotic foam macrophages and raising circulat-ing HDL (显示 HSD11B1 抗体) cholesterol levels.
Hepatic ABCA1 deficiency results in increased hepatic triglyceride and ANGPTL3 (显示 ANGPTL3 抗体) secretion, potentially underlying the elevated plasma triglyceride levels in Tangier disease patients.
ABCA1-derived nascent high-density lipoprotein-apolipoprotein AI (显示 APOA1 抗体) and lipids metabolically segregate.
Hepatic free cholesterol content was significantly increased in NASH (显示 SAMSN1 抗体) as compared to non-NASH (显示 SAMSN1 抗体) subjects, while ABCA1 and ABCG1 (显示 ABCG1 抗体) protein levels significantly decreased with NASH (显示 SAMSN1 抗体) and fibrosis progression. The relative expression of miR (显示 MLXIP 抗体)-33a and miR (显示 MLXIP 抗体)-144 correlated inversely with ABCA1 but not with ABCG1 (显示 ABCG1 抗体) protein levels. miR (显示 MLXIP 抗体)-33a/144 and their target gene ABCA1 may contribute to the pathogenesis of NASH (显示 SAMSN1 抗体) in morbidly obese subjects.
Understanding the relationship between cholesterol and inflammation in the lung, and the role that ABC (显示 ABCB6 抗体) transporters play in this may illuminate new pathways to target for the treatment of inflammatory lung diseases
ABCA1 was mainly located on trophoblast membranes. Decreased ABCA1 expression in trophoblasts reduced the cholesterol efflux of trophoblasts (P < 0.01). while increased ABCA1 expression in trophoblasts reduced the cholesterol efflux of trophoblasts (P < 0.05). ABCA1 was uniformly expressed on the cell membrane, cytoplasm, and nucleus of macrophages.
AMPK (显示 PRKAA1 抗体) activates LXRalpha (显示 NR1H3 抗体) and ABCA1 expression in human macrophages
Microparticles are lipoprotein-sized structures created by the ABCA1 transporter, and contribute approximately 30% of ABCA1-and apoA-I (显示 APOA1 抗体) mediated cholesterol efflux. MPs release from cells consists, in part, of exosomes and depends on the same pathway used for HDL (显示 HSD11B1 抗体) biogenesis.
there is an NFATc1 (显示 NFATC1 抗体)/ABCA1-dependent mechanism in which local TNF (显示 TNF 抗体) is sufficient to cause free cholesterol-dependent podocyte injury irrespective of TNF (显示 TNF 抗体), TNFR1 (显示 TNFRSF1A 抗体), or TNFR2 (显示 TNFRSF1B 抗体) serum levels
Reduced platelet count, but no major platelet function abnormalities, are associated with loss-of-function ATP-binding cassette-1 gene mutations.
our results highlight the importance of the LXR (显示 NR1H3 抗体)/ABCA1 system in brain pericytes and suggest a new role for these cells in brain cholesterol homeostasis.
The expression and distribution of the bovine ABCA1 transporter using quantitative PCR and the sequencing of the entire ABCA1 coding region, including the proximal promoter region, are reported.
Aortic endothelial cells transcytose high-density lipoproteins by mechanisms that involve either SR-BI (显示 SCARB1 抗体) or ABCG1 (显示 ABCG1 抗体) but not ABCA1.
ABCA1 promoter variants affect transcription activity and plasma HDL (显示 HSD11B1 抗体) level in pigs
ABCA1 was up-regulated in monocytes of hypercholesterolemic pigs via oxidized-LDL and prior to development coronary atherosclerosis.
Both region-specific and ubiquitous (ABCA1) phenotype changes were identified as early prelesional responses of the endothelium to hypercholesterolemia
CSL112 elevation of ABCA1-dependent efflux may target atherosclerotic plaque for cholesterol removal.
Rutaecarpine was identified to be a candidate that protected ApoE (显示 APOE 抗体)(-/-) mice from developing atherosclerosis through preferentially promoting activities of ABCA1 and SR-BI (显示 SCARB1 抗体) within RCT (显示 FOXE3 抗体).
Abca1 has a protective role in atherosclerosis, it exerts detrimental effects on cardiac function after myocardial infarction
Caveolin-1 (显示 CAV1 抗体) enhances internalization and degradation of ABCA1 by its association with ABCA1
an important role for hepatic ABCA1 in regulating secretory trafficking and modulating VLDL expansion during the TG accretion phase of hepatic lipoprotein particle assembly
These studies showed that following brain ischemia, reactive astrocytes become phagocytic and engulf debris via the ABCA1 pathway.
PCSK9 (显示 PCSK9 抗体) plays a direct role on Abca1-mediated cholesterol efflux through a downregulation of Abca1 gene and Abca1 protein expression. This extrahepatic effect may influence relevant steps in the pathogenesis of atherosclerosis, such as foam cell formation.
apoA-I (显示 APOA1 抗体)/ABCA1-mediated cholesterol efflux without STAT3 (显示 STAT3 抗体) activation can reduce proinflammatory cytokine expression in macrophages.
Our data indicate that a combination of vildagliptin and pravastatin significantly induces the expression of LXR (显示 NR1H3 抗体)-ABCA1/ABCG1 (显示 ABCG1 抗体) cascade and improves cholesterol efflux (P > 0.05) in adipocytes. Our data may explain, at least in part, the improvement in HDL (显示 HSD11B1 抗体)-C levels observed in patients receiving both medications
The findings obtained from apoE (显示 APOE 抗体)-/- mice provide epigenetic insights into how EZH2 (显示 EZH2 抗体) increases the risk of atherosclerotic heart disease. One of the pathways by which EZH2 (显示 EZH2 抗体) leads to lipid accumulation and foam cell formation is via epigenetic downregulation of ABCA1 expression.
The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. With cholesterol as its substrate, this protein functions as a cholesteral efflux pump in the cellular lipid removal pathway. Mutations in this gene have been associated with Tangier's disease and familial high-density lipoprotein deficiency.
ATP-binding cassette sub-family A member 1
, ATP-binding cassette transporter A1
, cholesterol efflux regulatory protein
, ATP-binding cassette, sub-family A (ABC1), member 1
, ATP-binding cassette, sub-family A member 1
, ATP-binding cassette transporter 1
, Cholesterol efflux regulatory protein
, ATP-binding cassette transporter
, ATP-binding cassette, sub-family A member 1-like
, ATP-binding cassette sub-family A member 1-like
, ATP-binding cassette 1