Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
Purification
This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
Immunogène
This ABCB11 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1038-1067 amino acids from the C-terminal region of human ABCB11.
anticorps ABCB11, anticorps Bsep, anticorps ABC16, anticorps BRIC2, anticorps BSEP, anticorps PFIC-2, anticorps PFIC2, anticorps PGY4, anticorps SPGP, anticorps Lith1, anticorps BSEP/SPGP, anticorps Spgp, anticorps ATP binding cassette subfamily B member 11, anticorps bile salt export pump, anticorps ATP-binding cassette, sub-family B (MDR/TAP), member 11, anticorps ABCB11, anticorps LOC100489744, anticorps LOC100565276, anticorps EDI_111220, anticorps EDI_272930, anticorps abcb11, anticorps Abcb11
Sujet
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.