Antibody data
- Antibody Data
- Antigen structure
- References [8]
- Comments [0]
- Validations
- Western blot [1]
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- Product number
- ABIN152887 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-ATP-Binding Cassette, Sub-Family G (WHITE), Member 8 (ABCG8) (N-Term) antibody
- Antibody type
- Polyclonal
- Description
- Immunogen affinity purified
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- N-Term
- Vial size
- 0.1 mL
- Storage
- Store at 4°C. Do not freeze.
- Handling
- Do not freeze.
Submitted references Identification of the Functions of Liver X Receptor-β in Sertoli Cells Using a Targeted Expression-Rescue Model.
Inhibition of post-translational N-glycosylation by HRD1 that controls the fate of ABCG5/8 transporter.
Role of the ABCG8 19H risk allele in cholesterol absorption and gallstone disease.
Regulation of intestinal NPC1L1 expression by dietary fish oil and docosahexaenoic acid.
Efflux of sphingomyelin, cholesterol, and phosphatidylcholine by ABCG1.
Role of ABCG1 and other ABCG family members in lipid metabolism.
Autosomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor protein.
Two genes that map to the STSL locus cause sitosterolemia: genomic structure and spectrum of mutations involving sterolin-1 and sterolin-2, encoded by ABCG5 and ABCG8, respectively.
Maqdasy S, El Hajjaji FZ, Baptissart M, Viennois E, Oumeddour A, Brugnon F, Trousson A, Tauveron I, Volle D, Lobaccaro JM, Baron S
Endocrinology 2015 Dec;156(12):4545-57
Endocrinology 2015 Dec;156(12):4545-57
Inhibition of post-translational N-glycosylation by HRD1 that controls the fate of ABCG5/8 transporter.
Suzuki S, Shuto T, Sato T, Kaneko M, Takada T, Suico MA, Cyr DM, Suzuki H, Kai H
Scientific reports 2014 Mar 3;4:4258
Scientific reports 2014 Mar 3;4:4258
Role of the ABCG8 19H risk allele in cholesterol absorption and gallstone disease.
Renner O, Lütjohann D, Richter D, Strohmeyer A, Schimmel S, Müller O, Stange EF, Harsch S
BMC gastroenterology 2013 Feb 13;13:30
BMC gastroenterology 2013 Feb 13;13:30
Regulation of intestinal NPC1L1 expression by dietary fish oil and docosahexaenoic acid.
Mathur SN, Watt KR, Field FJ
Journal of lipid research 2007 Feb;48(2):395-404
Journal of lipid research 2007 Feb;48(2):395-404
Efflux of sphingomyelin, cholesterol, and phosphatidylcholine by ABCG1.
Kobayashi A, Takanezawa Y, Hirata T, Shimizu Y, Misasa K, Kioka N, Arai H, Ueda K, Matsuo M
Journal of lipid research 2006 Aug;47(8):1791-802
Journal of lipid research 2006 Aug;47(8):1791-802
Role of ABCG1 and other ABCG family members in lipid metabolism.
Schmitz G, Langmann T, Heimerl S
Journal of lipid research 2001 Oct;42(10):1513-20
Journal of lipid research 2001 Oct;42(10):1513-20
Autosomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor protein.
Garcia CK, Wilund K, Arca M, Zuliani G, Fellin R, Maioli M, Calandra S, Bertolini S, Cossu F, Grishin N, Barnes R, Cohen JC, Hobbs HH
Science (New York, N.Y.) 2001 May 18;292(5520):1394-8
Science (New York, N.Y.) 2001 May 18;292(5520):1394-8
Two genes that map to the STSL locus cause sitosterolemia: genomic structure and spectrum of mutations involving sterolin-1 and sterolin-2, encoded by ABCG5 and ABCG8, respectively.
Lu K, Lee MH, Hazard S, Brooks-Wilson A, Hidaka H, Kojima H, Ose L, Stalenhoef AF, Mietinnen T, Bjorkhem I, Bruckert E, Pandya A, Brewer HB Jr, Salen G, Dean M, Srivastava A, Patel SB
American journal of human genetics 2001 Aug;69(2):278-90
American journal of human genetics 2001 Aug;69(2):278-90
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