You are viewing an incomplete version of our website. Please click to reload the website as full version.

ATP-Binding Cassette, Sub-Family G (WHITE), Member 8 Proteins (ABCG8)

The protein encoded by ABCG8 is a member of the superfamily of ATP-binding cassette (ABC) transporters. Additionally we are shipping ABCG8 Antibodies (62) and ABCG8 Kits (8) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
ABCG8 64241 Q9H221
ABCG8 67470 Q9DBM0
Rat ABCG8 ABCG8 155192 P58428
How to order from antibodies-online
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • Order online
  • orders@antibodies-online.com

Top ABCG8 Proteins at antibodies-online.com

Showing 4 out of 4 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
Insect Cells Human rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Log in to see 59 to 64 Days
$8,623.45
Details
HOST_Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
Insect Cells Mouse rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Log in to see 59 to 64 Days
$6,052.17
Details

ABCG8 Proteins by Origin and Source

Origin Expressed in Conjugate
Human ,
,
Mouse (Murine) ,
,

More Proteins for ATP-Binding Cassette, Sub-Family G (WHITE), Member 8 (ABCG8) Interaction Partners

Human ATP-Binding Cassette, Sub-Family G (WHITE), Member 8 (ABCG8) interaction partners

  1. Genetic polymorphism within the ABCG8 gene is a risk factor for diabetes.

  2. 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 Proteins) sterol transporter

  3. A polymorphism of the sterol transporter ABCG8 has been associated with the prevalence of end-stage renal disease

  4. Mutation in ABCG8 is associated with sitosterolaemia.

  5. ATP-binding cassette (ABC (show ABCB6 Proteins)) transporters G5 (ABCG5 (show ABCG5 Proteins)) and G8 (ABCG8) form an obligate heterodimer that limits intestinal absorption and facilitates biliary secretion of cholesterol and phytosterols.

  6. ABCG5 (show ABCG5 Proteins)/8 variants are associated with susceptibility to coronary heart disease.

  7. Sitosterolemia is caused by a genetic defect of sterolins (ABCG5 (show ABCG5 Proteins)/ABCG8) mapped to the STSL (show ABCG5 Proteins) locus. Polymorphic variations in STSL (show ABCG5 Proteins) have been linked to lipid levels and gallstone disease

  8. HRD1 (show SYVN1 Proteins) and RMA1 may therefore be negative regulators of disease-associated transporter ABCG5 (show ABCG5 Proteins)/ABCG8.

  9. MI and gallstones, 2 seemingly unrelated diseases, are intrinsically linked via the function of the ABCG5 (show ABCG5 Proteins)/8 cholesterol transporter.

  10. A single nucleotide polymorphism of ABCG8 is associated with fasting plasma glucose levels in a cross-sectional study but do not predict hyperglycemia or incident type 2 diabetes. [meta-analysis]

Mouse (Murine) ATP-Binding Cassette, Sub-Family G (WHITE), Member 8 (ABCG8) interaction partners

  1. ABCG5 (show ABCG5 Proteins)/G8 mediate mass biliary cholesterol secretion but not from a reverse cholesterol transport-relevant pool.

  2. AdGRP78 reduced expression of lipogenic genes and plasma triglycerides in the db/db (show LEPR Proteins) strain. Both G5 and G8 protein levels increased as did total biliary cholesterol

  3. The data demonstrate that Abcg5 (show ABCG5 Proteins)/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.

  4. Sitosterolemia is caused by a genetic defect of sterolins (ABCG5 (show ABCG5 Proteins)/ABCG8) mapped to the STSL locus. Polymorphic variations in STSL have been linked to lipid levels and gallstone disease

  5. The absence of an ABCG5 (show ABCG5 Proteins)/ABCG8 expression.

  6. biliary cholesterol mass secretion under maximal bile salt-stimulated conditions is fully dependent on ABCG5 (show ABCG5 Proteins)/G8

  7. This study is the first to report such toxic effects of phytosterol accumulation in ABCG5 (show ABCG5 Proteins)/G8 knockout mice.

  8. 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

  9. The ABCG5 (show ABCG5 Proteins) ABCG8 sterol transporter opposes the development of fatty liver disease and loss of glycemic control independently of phytosterol accumulation

  10. ABCG5 (show ABCG5 Proteins)/G8 deficiency in mice markedly raises triglyceride levels by impairing triglyceride catabolism and by increasing liver and intestinal triglyceride secretion.

Cow (Bovine) ATP-Binding Cassette, Sub-Family G (WHITE), Member 8 (ABCG8) interaction partners

  1. high expression levels of both ATP-binding cassette sub-family G member 5 (show ABCG5 Proteins) and 8 (ABCG5 (show ABCG5 Proteins) and ABCG8) were present in bovine liver and digestive tract samples, and in the mammary gland

ABCG8 Protein Profile

Protein Summary

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.

Gene names and symbols associated with ABCG8

  • ATP-binding cassette, sub-family G (WHITE), member 8 (ABCG8)
  • ATP-binding cassette sub-family G member 8 (PTRG_02054)
  • ABC transporter G family protein (abcG8)
  • ATP-binding cassette, sub-family G (WHITE), member 8 (abcg8)
  • ATP-binding cassette, sub-family G (WHITE), member 8 (Abcg8)
  • ATP-binding cassette, subfamily G (WHITE), member 8 (Abcg8)
  • 1300003C16Rik protein
  • AI114946 protein
  • DDBDRAFT_0167690 protein
  • DDBDRAFT_0191232 protein
  • DDB_0167690 protein
  • DDB_0191232 protein
  • GBD4 protein
  • sterolin-2 protein
  • STSL protein
  • zgc:172358 protein

Protein level used designations for ABCG8

ATP-binding cassette, sub-family G (WHITE), member 8 (sterolin 2) , sterolin 2 , ATP-binding cassette sub-family G member 8 , sterolin-2 , 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

GENE ID SPECIES
100069071 Equus caballus
421402 Gallus gallus
470363 Pan troglodytes
6338845 Pyrenophora tritici-repentis Pt-1C-BFP
8619568 Dictyostelium discoideum AX4
100033372 Monodelphis domestica
100136850 Danio rerio
100350554 Oryctolagus cuniculus
100402530 Callithrix jacchus
100445033 Pongo abelii
100466630 Ailuropoda melanoleuca
100601594 Nomascus leucogenys
64241 Homo sapiens
67470 Mus musculus
474571 Canis lupus familiaris
100048963 Sus scrofa
508829 Bos taurus
155192 Rattus norvegicus
Selected quality suppliers for ABCG8 Proteins (ABCG8)
Did you look for something else?