Anti-CD27 antibody [EPR27428-9] - BSA and Azide free
- Recombinant
- RabMAb
- What is this?
Be the first to review this product! Submit a review
|
(0 Publication)
Rabbit Recombinant Monoclonal CD27 antibody. Carrier free. Suitable for Flow Cyt, ICC/IF and reacts with Transfected cell line - Mouse, Human, Mouse, Rat samples.
View Alternative Names
CD27, Tnfrsf7, Cd27, CD27 antigen, CD27L receptor, T-cell activation antigen CD27, Tumor necrosis factor receptor superfamily member 7
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD27 antibody [EPR27428-9] - BSA and Azide free (AB316960)
This data was developed using ab316959, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Isotype (Left) / 293T cells transfected with a mouse CD27 expression vector containing a myc-His-tag® (Middle) / 293T cells transfected with an empty expression vector containing a myc-His-tag® (Right) cells labelling CD27 with ab316959 at 1/5000 dilution (0.01ug) / Middle and Right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control.
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Cells were co-stained with Myc tag conjugated to Alexa Fluor®647.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD27 antibody [EPR27428-9] - BSA and Azide free (AB316960)
This data was developed using ab316959, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Human PBMC (human peripheral blood mononuclear cell) cells labelling CD27 with ab316959 at 1/500 dilution (0.1ug)/right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control.
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Cells were co-stained with anti CD11b conjugated to BV510.
Gated on viable cells.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD27 antibody [EPR27428-9] - BSA and Azide free (AB316960)
This data was developed using ab316959, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Human PBMC (human peripheral blood mononuclear cell) cells labelling CD27 with ab316959 at 1/500 dilution (0.1ug)/right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control.
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Cells were co-stained with anti CD3 conjugated to Alexa Fluor®647.
Gated on viable cells.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD27 antibody [EPR27428-9] - BSA and Azide free (AB316960)
This data was developed using ab316959, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Mouse PBMC cells labelling CD27 with ab316959 at 1/500 dilution (0.1ug)/right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control.
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Cells were co-stained with anti CD11b conjugated to BV510.
Gated on viable cells.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD27 antibody [EPR27428-9] - BSA and Azide free (AB316960)
This data was developed using ab316959, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Mouse PBMC cells labelling CD27 with ab316959 at 1/500 dilution (0.1ug)/right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control.
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Cells were co-stained with anti CD3 conjugated to Alexa Fluor®647.
Gated on viable cells.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD27 antibody [EPR27428-9] - BSA and Azide free (AB316960)
This data was developed using ab316959, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Rat PBMC cells labelling CD27 with ab316959 at 1/500 dilution (0.1ug)/right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control.
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Cells were co-stained with anti CD3 conjugated to Alexa Fluor®647.
Gated on viable cells.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CD27 antibody [EPR27428-9] - BSA and Azide free (AB316960)
This data was developed using ab316959, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Tween-20 permeabilized mouse PBMC (Mouse primary peripheral blood mononuclear cell) cells labelling CD27 with ab316959 at 1/50 (9.94 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 ug/ml) dilution (Green).
Confocal image showing cytoplasmic staining in subsets of mouse PBMCs (shown in green), which is partly co-localised with CD3(shown in magenta). Nuclear DNA was labeled with DAPI (shown in blue).
Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8).
Anti-rat CD3 mouse monoclonal antibody (Alexa Fluor® 647) was used to counterstain at 1/100 (5ug/ml) dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/ml) dilution.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CD27 antibody [EPR27428-9] - BSA and Azide free (AB316960)
This data was developed using ab316959, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Tween-20 permeabilized mouse PBMC (Mouse primary peripheral blood mononuclear cell) cells labelling CD27 with ab316959 at 1/50 (9.94 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 ug/ml) dilution (Green).
Confocal image showing cytoplasmic staining in subsets of mouse PBMCs (shown in green), which is not co-localised with CD11b (shown in magenta). Nuclear DNA was labeled with DAPI (shown in blue).
Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8).
ab8878 Anti-CD11b Rat monoclonal antibody was used to counterstain at 1/200 (2.5ug/ml) dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/ml) dilution.
Related conjugates and formulations (5)
-
Anti-CD27 antibody [EPR27428-9]
-
519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-CD27 antibody [EPR27428-9]
-
617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-CD27 antibody [EPR27428-9]
-
665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-CD27 antibody [EPR27428-9]
-
578 PE
PE Anti-CD27 antibody [EPR27428-9]
Reactivity data
Product details
ab316960 is the carrirer-free version of ab316959.
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
One finds CD27 at the heart of cellular immune responses. It does not function alone; instead it typically forms part of a receptor-ligand complex with CD70 which influences T cell and B cell activities. This interaction promotes cell survival and plays a role in the activation of NF-kB and MAPK8/JNK signaling pathways which are essential for immune response regulation. These pathways ensure that the body's immune cells can efficiently respond to pathogens.
Pathways
CD27 actively integrates into the NF-kB and mTOR signaling pathways which are important for regulating immune and inflammatory responses. Through these pathways CD27 works closely with proteins like TRAF2 and TRAF3 which are adapter molecules that transmit signals from the receptor. These signaling pathways provide a framework for understanding how CD27 and associated proteins work together to control immune cell behavior facilitating coordinated immune defense mechanisms.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
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