ARG45828

anti-Zebrafish ABCB11 antibody

anti-Zebrafish ABCB11 antibody for IHC-Formalin-fixed paraffin-embedded sections and Zebrafish

Overview

Product Description Rabbit Polyclonal antibody recognizes ABCB11
Tested Reactivity Zfsh
Tested Application IHC-P
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name ABCB11
Antigen Species Zebrafish
Conjugation Un-conjugated
Alternate Names ABCB11; ATP-binding cassette, sub-family B (MDR/TAP), member 11; SPGP; ABC16; BRIC2; PGY4; Bile salt export pump; PFIC2; PFIC-2; ATP-binding cassette sub-family B member 11; BSEP

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P2-5 μg/ml
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Affinity chromatography purified
Buffer 0.9% NaCl, 0.2% Na2HPO4, 0.02% Sodium azide and 50% glycerol.
Preservative 0.02% Sodium azide
Stabilizer 50% glycerol
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Gene Symbol ABCB11
Gene Full Name ATP-binding cassette, sub-family B (MDR/TAP), member 11
Background The membrane-associated 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 MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is the major canalicular bile salt export pump in man. Mutations in this gene cause a form of progressive familial intrahepatic cholestases which are a group of inherited disorders with severe cholestatic liver disease from early infancy. [provided by RefSeq, Jul 2008]
Function Involved in the ATP-dependent secretion of bile salts into the canaliculus of hepatocytes. [UniProt]
Cellular Localization Endosomeautomatic annotation; Membrane. [UniProt]
Calculated MW 146 kDa
PTM Ubl conjugation. [UniProt]