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The protein encoded by ABCG8 is a member of the superfamily of ATP-binding cassette (ABC) transporters. Additionally we are shipping ABCG8 Proteins (6) and many more products for this protein.
Showing 10 out of 78 products:
Human Monoclonal ABCG8 Primary Antibody for ICC, IF - ABIN4277252
Graf, Yu, Li, Gerard, Tuma, Cohen, Hobbs: ABCG5 and ABCG8 are obligate heterodimers for protein trafficking and biliary cholesterol excretion. in The Journal of biological chemistry 2003
Show all 7 Pubmed References
Human Polyclonal ABCG8 Primary Antibody for ICC, IF - ABIN152894
Mathur, Watt, Field: Regulation of intestinal NPC1L1 expression by dietary fish oil and docosahexaenoic acid. in Journal of lipid research 2007
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Human Polyclonal ABCG8 Primary Antibody for WB - ABIN152887
Garcia, Wilund, Arca, Zuliani, Fellin, Maioli, Calandra, Bertolini, Cossu, Grishin, Barnes, Cohen, Hobbs: Autosomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor protein. in Science (New York, N.Y.) 2001
Show all 8 Pubmed References
Polyclonal ABCG8 Primary Antibody for WB - ABIN540800
Remaley, Bark, Walts, Freeman, Shulenin, Annilo, Elgin, Rhodes, Joyce, Dean, Santamarina-Fojo, Brewer: Comparative genome analysis of potential regulatory elements in the ABCG5-ABCG8 gene cluster. in Biochemical and biophysical research communications 2002
Show all 5 Pubmed References
Human Polyclonal ABCG8 Primary Antibody for ICC, IF - ABIN4277253
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 ABCG8 Primary Antibody for WB - ABIN438154
Maqdasy, El Hajjaji, Baptissart, Viennois, Oumeddour, Brugnon, Trousson, Tauveron, Volle, Lobaccaro, Baron: Identification of the Functions of Liver X Receptor-β in Sertoli Cells Using a Targeted Expression-Rescue Model. in Endocrinology 2015
ABCG8 genetic variants may have role in the development of cholelithiasis in patients with Gaucher disease type 1.
Genetic polymorphism within the ABCG8 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 (show ABCB6 Antibodies) sterol transporter
A polymorphism of the sterol transporter ABCG8 has been associated with the prevalence of end-stage renal disease
Mutation in ABCG8 is associated with sitosterolaemia.
ATP-binding cassette (ABC (show ABCB6 Antibodies)) transporters G5 (ABCG5 (show ABCG5 Antibodies)) and G8 (ABCG8) form an obligate heterodimer that limits intestinal absorption and facilitates biliary secretion of cholesterol and phytosterols.
ABCG5 (show ABCG5 Antibodies)/8 variants are associated with susceptibility to coronary heart disease.
Sitosterolemia is caused by a genetic defect of sterolins (ABCG5 (show ABCG5 Antibodies)/ABCG8) mapped to the STSL (show ABCG5 Antibodies) locus. Polymorphic variations in STSL (show ABCG5 Antibodies) have been linked to lipid levels and gallstone disease
HRD1 (show SYVN1 Antibodies) and RMA1 may therefore be negative regulators of disease-associated transporter ABCG5 (show ABCG5 Antibodies)/ABCG8.
MI and gallstones, 2 seemingly unrelated diseases, are intrinsically linked via the function of the ABCG5 (show ABCG5 Antibodies)/8 cholesterol transporter.
The ABCG5 (show ABCG5 Antibodies)/G8-independent pathway plays an important role in regulating biliary cholesterol secretion, and gallstone formation, which works independently of the ABCG5 (show ABCG5 Antibodies)/G8 pathway.
ABCG5 (show ABCG5 Antibodies)/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 (show LEPR Antibodies) strain. Both G5 and G8 protein levels increased as did total biliary cholesterol
The data demonstrate that Abcg5 (show ABCG5 Antibodies)/Abcg8 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 (show ABCG5 Antibodies)/ABCG8) mapped to the STSL locus. Polymorphic variations in STSL have been linked to lipid levels and gallstone disease
The absence of an ABCG5 (show ABCG5 Antibodies)/ABCG8 expression.
biliary cholesterol mass secretion under maximal bile salt-stimulated conditions is fully dependent on ABCG5 (show ABCG5 Antibodies)/G8
This study is the first to report such toxic effects of phytosterol accumulation in ABCG5 (show ABCG5 Antibodies)/G8 knockout mice.
handling of sterols by the intestine involves both G5G8 and ACAT2 but that an additional factor (possibly Niemann-Pick C1-like 1) may be key in determining absorption efficiency
The ABCG5 (show ABCG5 Antibodies) ABCG8 sterol transporter opposes the development of fatty liver disease and loss of glycemic control independently of phytosterol accumulation
high expression levels of both ATP-binding cassette sub-family G member 5 (show ABCG5 Antibodies) and 8 (ABCG5 (show ABCG5 Antibodies) and ABCG8) were present in bovine liver and digestive tract samples, and in the mammary gland
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 to exclude non-cholesterol sterol entry at the intestinal level, promote excretion of cholesterol and sterols into bile, and to facilitate transport of sterols back into the intestinal lumen. It is expressed in a tissue-specific manner in the liver, intestine, and gallbladder. This gene is tandemly arrayed on chromosome 2, in a head-to-head orientation with family member ABCG5. Mutations in this gene may contribute to sterol accumulation and atherosclerosis, and have been observed in patients with sitosterolemia.
ATP-binding cassette, sub-family G (WHITE), member 8 (sterolin 2)
, sterolin 2
, ATP-binding cassette sub-family G member 8
, ATP-binding cassette, sub-family G (WHITE), member 8
, ATP-binding cassette sub-family G member 8-like
, ATP-binding cassette, subfamily G, member 8