Anti-ABCB11/BSEP antibody [EPR22670-64] - BSA and Azide free (ab256536)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR22670-64] to ABCB11/BSEP - BSA and Azide free
- Suitable for: Flow Cyt (Intra), IHC-P, ICC/IF
- Reacts with: Human
Overview
-
Product name
Anti-ABCB11/BSEP antibody [EPR22670-64] - BSA and Azide free
See all ABCB11/BSEP primary antibodies -
Description
Rabbit monoclonal [EPR22670-64] to ABCB11/BSEP - BSA and Azide free -
Host species
Rabbit -
Tested applications
Suitable for: Flow Cyt (Intra), IHC-P, ICC/IFmore details
Unsuitable for: IP or WB -
Species reactivity
Reacts with: Human -
Immunogen
Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.
-
Positive control
- IHC-P: Human hepatocellular carcinoma and liver tissue. ICC/IF: HEK-293T cells transfected with myc-tagged BSEP. Flow Cyt (intra): HEK-293T cells transfected with myc-tagged BSEP.
-
General notes
ab256536 is the carrier-free version of ab255605.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Properties
-
Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. Do Not Freeze. -
Storage buffer
pH: 7.2
Constituent: PBS -
Carrier free
Yes -
Concentration information loading...
-
Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
EPR22670-64 -
Isotype
IgG -
Research areas
Images
-
Immunohistochemical analysis of paraffin-embedded human liver tissue labeling BSEP with ab255605 at 1/500 dilution (1.288µg/ml) followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP). Positive staining in canaliculi of human liver (PMID: 26182153) is observed. Counterstained with hematoxylin. Heat mediated antigen retrieval using ab93684 (Tris/EDTA buffer, pH 9.0).
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab255605).
-
Immunohistochemical analysis of paraffin-embedded human hepatocellular carcinoma tissue labeling BSEP with ab255605 at 1/ 500 dilution (1.288µg/ml) followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP). Positive staining in canaliculi of human hepatocellular carcinoma (PMID: 26735860) is observed.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab255605).
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
-
Immunohistochemical analysis of paraffin-embedded human cholangiocarcinomas tissue labeling BSEP with ab255605 at 1/500 dilution (1.288µg/ml) followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP). Negative staining in human cholangiocarcinomas (PMID: 26735860) is observed. Counterstained with hematoxylin. Heat mediated antigen retrieval using ab93684 (Tris/EDTA buffer, pH 9.0).
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab255605).
-
Flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol permeabilized HEK-293T (human embryonic kidney epithelial cell) transfected with myc-tagged BSEP expression vector cells labeling BSEP with ab255605 at 1/600 dilution (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as the secondary antibody. Gated on myc(+) population.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab255605).
-
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HEK-293T (human embryonic kidney epithelial cell) cells labeling BSEP with ab255605 at 1/100, (6.4µg/ml) dilution, followed by ab150077 AlexaFluor® 488 Goat anti-Rabbit secondary antibody at 1/1000, (2µg/ml) dilution (Green). Confocal image showing membranous and cytoplasmic staining in 293T cells transfected with myc-tagged BSEP expression vector. ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (Red). The nuclear counterstain was DAPI (Blue).
Negative control: myc-transfected cells.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is ab150077 AlexaFluor® 488 Goat anti-Rabbit secondary at 1/1000, 2µg/ml dilution.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab255605).
-