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The protein encoded by ABCG1 is a member of the superfamily of ATP-binding cassette (ABC) transporters. Additionally we are shipping ABCG1 Kits (34) and ABCG1 Proteins (9) and many more products for this protein.
Showing 10 out of 99 products:
Chinese Hamster Polyclonal ABCG1 Primary Antibody for ICC, IF - ABIN152900
Hu, Abe-Dohmae, Tsujita, Iwamoto, Ogikubo, Otsuka, Kumon, Yokoyama: Biogenesis of HDL by SAA is dependent on ABCA1 in the liver in vivo. in Journal of lipid research 2008
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Human Polyclonal ABCG1 Primary Antibody for IF (p), IHC (p) - ABIN673719
Jia, Song, Yang, Ma, Li, Lu, Cao, Zhang, Zhu, Wang, Leng, Cao, Du, Xu: Effects of Tanshinone IIA on the modulation of miR‑33a and the SREBP‑2/Pcsk9 signaling pathway in hyperlipidemic rats. in Molecular medicine reports 2016
Aortic endothelial cells transcytose high-density lipoproteins by mechanisms that involve either SR-BI (show SCARB1 Antibodies) or ABCG1 but not ABCA1 (show ABCA1 Antibodies).
High ABCG1 expression is associated with glioma.
ABCG1 regulates pulmonary surfactant metabolism
Hepatic free cholesterol content was significantly increased in NASH (show SAMSN1 Antibodies) as compared to non-NASH (show SAMSN1 Antibodies) subjects, while ABCA1 (show ABCA1 Antibodies) and ABCG1 protein levels significantly decreased with NASH (show SAMSN1 Antibodies) and fibrosis progression. The relative expression of miR (show MLXIP Antibodies)-33a and miR (show MLXIP Antibodies)-144 correlated inversely with ABCA1 (show ABCA1 Antibodies) but not with ABCG1 protein levels. miR (show MLXIP Antibodies)-33a/144 and their target gene ABCA1 (show ABCA1 Antibodies) may contribute to the pathogenesis of NASH (show SAMSN1 Antibodies) in morbidly obese subjects.
Understanding the relationship between cholesterol and inflammation in the lung, and the role that ABC (show ABCB6 Antibodies) transporters play in this may illuminate new pathways to target for the treatment of inflammatory lung diseases
Findings suggest that the ABCG1-mediated efflux of cholesterol, but not of 7-ketocholesterol, shows specificity for structural domains of apoA-I (show APOA1 Antibodies) bound to reconstituted HDL (show HSD11B1 Antibodies). Although the mid region alone of apoA-I (show APOA1 Antibodies) associated to rHDL can promote ABCG1-mediated cholesterol efflux, deletion of carboxyl-terminal region 185-243 from full-length apoA-I (show APOA1 Antibodies) diminishes ABCG1-mediated cholesterol efflux.
ABCG1 regulates T cell differentiation into Tregs, highlighting a pathway by which cholesterol accumulation can influence T cell homeostasis in atherosclerosis
Data show that ELOVL7 (show ELOVL7 Antibodies), SOCS3 (show SOCS3 Antibodies), ACSL4 (show ACSL4 Antibodies) and CLU (show CLU Antibodies) were upregulated while PRKAR1A (show PRKAR1A Antibodies) and ABCG1 were downregulated in the phlegm-dampness group.
ABCG1 and ABCG4 (show ABCG4 Antibodies) alter the distribution of gamma-secretase on the plasma membrane, leading to the decreased gamma-secretase activity and suppressed Abeta (show APP Antibodies) secretion
Both the full-length and the short isoforms of ABCG1 can dimerize with ABCG4 (show ABCG4 Antibodies), whereas the ABCG2 (show ABCG2 Antibodies) multidrug transporter is unable to form a heterodimer with ABCG4 (show ABCG4 Antibodies).
DNA methylation (show HELLS Antibodies) at the ABCG1 locus cg06500161 in blood DNA was associated with an increased risk for future type2 diabetes.
Our data indicate that a combination of vildagliptin and pravastatin significantly induces the expression of LXR (show NR1H3 Antibodies)-ABCA1 (show ABCA1 Antibodies)/ABCG1 cascade and improves cholesterol efflux (P > 0.05) in adipocytes. Our data may explain, at least in part, the improvement in HDL (show HSD11B1 Antibodies)-C levels observed in patients receiving both medications
ABCG1 may play a protective role in early-stage atherosclerosis by reducing endothelial activation induced by oscillatory shear stress via suppressing the inflammatory response.
Endothelial cholesterol efflux pathways mediated by ABCA1 (show ABCA1 Antibodies) and ABCG1 are nonredundant and atheroprotective, reflecting preservation of endothelial NO synthase (show NOS Antibodies) activity and suppression of endothelial inflammation, especially in regions of disturbed arterial blood flow.
ABCG1, irrespective of either a leucine or proline at position 550, is an intracellular protein (show CKAP2 Antibodies) that localizes to vesicles of the endosomal pathway where it functions to mobilize sterols away from the endoplasmic reticulum and out of the cell.
our study suggests that MEK1 (show MAP2K1 Antibodies)/2 inhibitors activate macrophage ABCG1 expression/RCT (show FOXE3 Antibodies), and inhibit foam cell formation and lesion development by multiple mechanisms, supporting the concept that ERK1/2 (show MAPK1/3 Antibodies) inhibition is anti-atherogenic
miR-33 augments macrophage lipid rafts and enhances proinflammatory cytokine induction and NF-kappaB activation by LPS. This occurs through an ABCA1- and ABCG1-dependent mechanism and is reversible by interventions upon raft cholesterol and by ABC transporter-inducing liver X receptor agonists.
ABCG1 expression was down-regulated by TLR4 (show TLR4 Antibodies), which induces inflammation and lipid accumulation in vascular smooth muscle cells via PPARgamma (show PPARG Antibodies)/LXRalpha (show NR1H3 Antibodies) signaling.
Visfatin (show NAMPT Antibodies) upregulated CD36 (show CD36 Antibodies) and SRA (show MSR1 Antibodies) expression and downregulated ABCA1 (show ABCA1 Antibodies) and ABCG1 expression, subsequently increased ox-LDL uptake and decreased cholesterol efflux, and finally promoted foam cell formation via the PI3K- and ERK (show EPHB2 Antibodies)-dependent pathways.
The 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 intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the White subfamily. It is involved in macrophage cholesterol and phospholipids transport, and may regulate cellular lipid homeostasis in other cell types. Six alternative splice variants have been identified.
ATP-binding cassette sub-family G member 1
, ATP-binding cassette, sub-family G (WHITE), member 1
, ATP-binding cassette sub-family G member 1-like
, ABC transporter 8
, ATP-binding cassette transporter 8
, ATP-binding cassette transporter member 1 of subfamily G
, homolog of Drosophila white
, white protein homolog (ATP-binding cassette transporter 8)
, ATP-binding cassette 8
, ATP-binding cassette, subfamily G, member 1
, white protein homolog