Anti-PD-L1 antibody [EPR23546-160] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal PD-L1 antibody. Carrier free. Suitable for ICC/IF, Flow Cyt and reacts with Mouse samples.
View Alternative Names
CD274, B7h1, Pdcd1l1, Pdcd1lg1, Pdl1, Cd274, Programmed cell death 1 ligand 1, PD-L1, PDCD1 ligand 1, Programmed death ligand 1, B7 homolog 1, B7-H1
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-PD-L1 antibody [EPR23546-160] - BSA and Azide free (AB275384)
This data was developed using ab252436, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized RAW 264.7 cells labelling PD-L1 with ab252436 at 1/50 (10.42 ug/ml) dilution, followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution (Green). Confocal image showing membranous staining in RAW 264.7 cell line after treatment with IFN-γ (100 ng/ml) for 24h. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.
- Flow Cyt
Unknown
Flow Cytometry - Anti-PD-L1 antibody [EPR23546-160] - BSA and Azide free (AB275384)
This data was developed using ab252436, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of A20 (Mouse reticulum sarcoma B lymphocyte) cells labelling PD-L1 with ab252436 at 1/500 dilution (0.1ug) (Red), compared with a Rabbit monoclonal IgG (ab172730) isotype contro l(Black), and an unlabelled 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 viable cells.
- Flow Cyt
Unknown
Flow Cytometry - Anti-PD-L1 antibody [EPR23546-160] - BSA and Azide free (AB275384)
This data was developed using ab252436, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Mouse splenocyte cells labelling PD-L1 with ab252436 at 1/500 dilution (0.1ug) (Right) compared with a Rabbit monoclonal IgG (ab172730) isotype control (Left).
A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as the secondary antibody.
Gated on viable MHC II (I-A/I-E) positive cells.PD-L1 is highly expressed on DC cells as described in literature (PMID : 22902234).
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-PD-L1 antibody [EPR23546-160] - BSA and Azide free (AB275384)
This data was developed using ab252436, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized A20 cells labelling PD-L1 with ab252436 at 1/50 (10.42 ug/ml) dilution, followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution (Green). Confocal image showing membranous staining in A20 cell line. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.
- Flow Cyt
Lab
Flow Cytometry - Anti-PD-L1 antibody [EPR23546-160] - BSA and Azide free (AB275384)
This data was developed using ab252436, the same antibody clone in a different buffer formulation.
Flow cytometry staining of C57BL/6 mouse splenocytes with ab252436 (right) or Recombinant Rabbit IgG, monoclonal [EPR25A] - Isotype Control (left). Cells were incubated for 30 min on ice in 1x PBS containing 10μg/ml anti CD16/CD32 and 10% normal goat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody ab252436 or Recombinant Rabbit IgG, monoclonal [EPR25A] - Isotype Control (1x 106in 100 μl at 10.0 μg/ml (1/209)) for 30min on ice. The cells were simultaneously stained with CD3.
The secondary antibody Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed was incubated at 1/4000 for 30min on ice
Acquisition of >30000 events were collected using a 50 mW Blue laser (488nm) and 525/40 bandpass filter. Events were gated on live cells.
Related conjugates and formulations (2)
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Anti-PD-L1 antibody [EPR23546-160]
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Anti-PD-L1 antibody [EPR23546-160] - BSA and Azide free (Detector)
Reactivity data
Product details
ab275384 is the carrier-free version of ab252436.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
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 batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. 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 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
PD-L1 plays a central role in immune evasion mechanisms utilized by tumors. It is not part of a larger protein complex but directly interacts with PD-1 and CD80. When PD-L1 binds to PD-1 it sends inhibitory signals leading to decreased T cell activation and proliferation allowing cancer cells to avoid immune destruction. PD-L1 expression provides a mechanism for tumors to suppress immune surveillance facilitating tumor progression.
Pathways
PD-L1 is integral to the immune checkpoint pathway which is an important regulator of immune response. The interaction between PD-L1 and PD-1 provides a mechanism for immune tolerance which is part of the broader adaptive immune system pathway. PD-L1 is related to other immune checkpoint proteins such as CTLA-4 in its function to limit autoreactivity and promote immune homeostasis.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com