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The protein encoded by ABCG5 is a member of the superfamily of ATP-binding cassette (ABC) transporters. Zusätzlich bieten wir Ihnen ABCG5 Proteine (5) und ABCG5 Kits (1) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 45 products:
Human Polyclonal ABCG5 Primary Antibody für IF (p), IHC (p) - ABIN708371
Wang, Xiaoling, Pingting, Shuqiang, Yuaner: Chronic unpredictable mild stress combined with a high-fat diets aggravates atherosclerosis in rats. in Lipids in health and disease 2014
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Human Monoclonal ABCG5 Primary Antibody für FACS, IHC - ABIN1724857
Johnson, Lee, Pickert, Urbatsch: Bile acids stimulate ATP hydrolysis in the purified cholesterol transporter ABCG5/G8. in Biochemistry 2010
Show all 2 Pubmed References
Human Polyclonal ABCG5 Primary Antibody für IHC, IHC (p) - ABIN4277248
Ahn, Jang, Jun, Lee, Shin: Expression of liver X receptor correlates with intrahepatic inflammation and fibrosis in patients with nonalcoholic fatty liver disease. in Digestive diseases and sciences 2014
Human Polyclonal ABCG5 Primary Antibody für WB - ABIN4892532
Huang, Wang, Quan, Wang, Yang, Zhong: Lactobacillus acidophilus ATCC 4356 prevents atherosclerosis via inhibition of intestinal cholesterol absorption in apolipoprotein E-knockout mice. in Applied and environmental microbiology 2014
ABCG5 gene variants were not associated with cholelithiasis in patients with Gaucher disease type 1.
Genetic variations in ABCG5, CYP7A1 (zeige CYP7A1 Antikörper), and DHCR7 (zeige DHCR7 Antikörper) may contribute to differing responses of serum cholesterol to dairy intake among healthy adults.
ABCG5 Gene Variants are associated with Sitosterolemia and Familial Mediterranean Fever (zeige MEFV Antikörper).
first case of a Mexican family with sitosterolemia carrying two new ABCG5 gene mutations
Genetic polymorphism within the ABCG5 gene is a risk factor for diabetes.
crystallization in lipid bilayers to determine the X-ray structure of human G5G8 in a nucleotide-free state at 3.9 A resolution, generating the first atomic model of an ABC (zeige ABCB6 Antikörper) sterol transporter
ATP-binding cassette (ABC (zeige ABCB6 Antikörper)) transporters G5 (ABCG5) and G8 (ABCG8 (zeige ABCG8 Antikörper)) form an obligate heterodimer that limits intestinal absorption and facilitates biliary secretion of cholesterol and phytosterols.
ABCG5/8 variants are associated with susceptibility to coronary heart disease.
Sitosterolemia is caused by a genetic defect of sterolins (ABCG5/ABCG8 (zeige ABCG8 Antikörper)) mapped to the STSL locus. Polymorphic variations in STSL have been linked to lipid levels and gallstone disease
HRD1 (zeige SYVN1 Antikörper) and RMA1 may therefore be negative regulators of disease-associated transporter ABCG5/ABCG8 (zeige ABCG8 Antikörper).
high expression levels of both ATP-binding cassette sub-family G member 5 and 8 (ABCG5 and ABCG8 (zeige ABCG8 Antikörper)) were present in bovine liver and digestive tract samples, and in the mammary gland
ABCG5 and ABCG8 (zeige ABCG8 Antikörper) mRNA levels were significantly increased in cholesterol group and less increased in myriocin group, relative to that in normal group.
The ABCG5/G8-independent pathway plays an important role in regulating biliary cholesterol secretion, and gallstone formation, which works independently of the ABCG5/G8 pathway.
ABCG5/G8 mediate mass biliary cholesterol secretion but not from a reverse cholesterol transport-relevant pool.
AdGRP78 reduced expression of lipogenic genes and plasma triglycerides in the db/db (zeige LEPR Antikörper) strain. Both G5 and G8 protein levels increased as did total biliary cholesterol
The data demonstrate that Abcg5/Abcg8 (zeige ABCG8 Antikörper) deficiency reduces the uptake and secretion of both dietary triacylglycerols and cholesterol by the intestine, suggesting a novel role for the sterol transporter in the formation and secretion of chylomicrons.
Sitosterolemia is caused by a genetic defect of sterolins (ABCG5/ABCG8 (zeige ABCG8 Antikörper)) mapped to the STSL (zeige ABCG8 Antikörper) locus. Polymorphic variations in STSL (zeige ABCG8 Antikörper) have been linked to lipid levels and gallstone disease
The absence of an ABCG5/ABCG8 (zeige ABCG8 Antikörper) expression.
Mice with deficient Abcg2 (zeige ABCG2 Antikörper) have features of inflammatory DCM and that the reversibility of myocardial T cell infiltration provides a novel model for investigating the progression of myocardial fibrosis.
biliary cholesterol mass secretion under maximal bile salt-stimulated conditions is fully dependent on ABCG5/G8
This study is the first to report such toxic effects of phytosterol accumulation in ABCG5/G8 knockout mice.
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. The protein encoded by this gene functions as a half-transporter to limit intestinal absorption and promote biliary excretion of sterols. It is expressed in a tissue-specific manner in the liver, colon, and intestine. This gene is tandemly arrayed on chromosome 2, in a head-to-head orientation with family member ABCG8. Mutations in this gene may contribute to sterol accumulation and atheroschlerosis, and have been observed in patients with sitosterolemia.
ATP-binding cassette, sub-family G (WHITE), member 5 (sterolin 1)
, ATP-binding cassette sub-family G member 5
, sterolin 1
, ATP-binding cassette transporter
, ATP-binding cassette, sub-family G (WHITE), member 5
, ATP-binding cassette sub-family G member 5-like
, ATP-binding cassette, subfamily G, member 5
, ATP-binding cassette sub-family G (WHITE) member 5 (sterolin 1)