ATP-Binding Cassette, Sub-Family B (MDR/TAP), Member 11 (ABCB11) (C-Term) Peptide
| Name | ATP-Binding Cassette, Sub-Family B (MDR/TAP), Member 11 (ABCB11) |
| Synonyms | BSEP, PGY4, SPGP, ABC16, BRIC2, PFIC2, PFIC-2, Bsep, Lith1, Spgp, ABCB11, BSEP/SPGP |
| Binding Site |
C-Term |
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1 reference available |
| Certificates | ISO 9001:2008 |
| Catalog no. | ABIN695581 |
| Quantity | 0.1 mg |
| Price | 49.50 $ Plus shipping costs $45.00 |
| Shipping to |
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| Availability | Will be delivered in 2 to 3 Business Days |
Additional Information
| Immunogen | Synthetic peptide |
| Characteristics | Blocking peptide for ABCB11 (C-term) antibody ABIN390059 |
| Specificity | The synthetic peptide sequence used to generate the antibody AP6110a was selected from the C-term region of human ABCB11 . A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay. |
| Comments |
Background: ABCB11 is involved in the ATP-dependent secretion of bile salts into the canaliculus of hepatocytes. It is expressed predominatly, if not exclusively, in the liver, where it is further localized to the canilicular microvilli and to subcanilicular vesicles fo the hepatocytes. Structurally, ABCB11 is a multifunctional polypeptide with two homologus halves, each containing a hydrophobic membrane-anchoring domain and an ATP binding cassette (ABC) domain. Defects in ABCB11 are the cause of progressive familial intrahepatic cholestasis 2 (PFIC2). PFIC2 is an inherited liver disease of childhood which is characterized by cholestasis and normal serum gamma-glutamyltransferase activity. Defects in ABCB11 are also found in cases of chronic intrahepatic cholestasis without obvious familial history of chronic liver disease. |
Application Details
| Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles |
| Restrictions | For Research Use only |
Publications
| Product |
Strautnieks, Bull, Knisely et al.: "A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis." in: Nature genetics, Vol. 20, Issue 3, pp. 233-8, 1998 (PubMed).
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