Anti-ADA2 antibody [EPR25430-131] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal CECR1 antibody. Carrier free. Suitable for Flow Cyt (Intra), IHC-P, WB and reacts with Human samples.
View Alternative Names
ADGF, CECR1, IDGFL, ADA2, Adenosine deaminase 2, Cat eye syndrome critical region protein 1
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ADA2 antibody [EPR25430-131] - BSA and Azide free (AB288305)
This data was developed using 288296, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human skeletal muscle tissue labelling ADA2 with ab288296 (0.259 μg/ml) at 1/2000 dilution followed by a ready to use LeicaDS9800 (Bond®, Polymer Refine Detection). Negative control : No staining on human skeletal muscle. The section was incubated with ab288296 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond®, Polymer Refine Detection) was used.
Antigen Retrieval : Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ADA2 antibody [EPR25430-131] - BSA and Azide free (AB288305)
This data was developed using 288296, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human tonsil tissue labelling ADA2 with ab288296 at 1/2000 dilution followed by a ready to use LeicaDS9800 (Bond®, Polymer Refine Detection). Cytoplasmic staining on human tonsil. The section was incubated with ab288296 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond®, Polymer Refine Detection).
Antigen Retrieval : Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ADA2 antibody [EPR25430-131] - BSA and Azide free (AB288305)
This data was developed using 288296, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human colon tissue labelling ADA2 with ab288296 (0.259 μg/ml) at 1/2000 dilution followed by a ready to use LeicaDS9800 (Bond®, Polymer Refine Detection). Cytoplasmic staining on human colon. The section was incubated with ab288296 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond®, Polymer Refine Detection).
Antigen Retrieval : Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-ADA2 antibody [EPR25430-131] - BSA and Azide free (AB288305)
This data was developed using 288296, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized HUVEC (human umbilical vein endothelial cell, Left) / MOLT-4 (human lymphoblastic leukemia T lymphoblast, Right) cells labelling ADA2 with ab288296 at 1/50 dilution (1μg)(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, ab150081) at 1/2000 dilution was used as the secondary antibody.
Low expression : HUVEC (PMID : 24552284, 32743071).
- WB
Supplier Data
Western blot - Anti-ADA2 antibody [EPR25430-131] - BSA and Azide free (AB288305)
This data was developed using 288296, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Exposure time : Lane 1-2 : 70 seconds; Lane 3 : 7.75 seconds
All lanes:
Western blot - Anti-ADA2 antibody [EPR25430-131] (<a href='/en-us/products/primary-antibodies/ada2-antibody-epr25430-131-ab288296'>ab288296</a>) at 1/1000 dilution
Lane 1:
Human plasma at 20 µL
Lane 2:
Human heart tissue lysate at 20 µg
Lane 3:
Human lung tissue lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Predicted band size: 58 kDa
Observed band size: 58 kDa
false
- WB
Supplier Data
Western blot - Anti-ADA2 antibody [EPR25430-131] - BSA and Azide free (AB288305)
This data was developed using 288296, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Low expression : HUVEC(PMID : 24552284, 32743071)
Exposure time : 5.5 seconds
All lanes:
Western blot - Anti-ADA2 antibody [EPR25430-131] (<a href='/en-us/products/primary-antibodies/ada2-antibody-epr25430-131-ab288296'>ab288296</a>) at 1/1000 dilution
Lane 1:
MOLT-4 (human lymphoblastic leukemia T lymphoblast) whole cell lysate at 20 µg
Lane 2:
THP-1 (human monocytic leukemia monocyte) whole cell lysate at 20 µg
Lane 3:
U937 (human histiocytic lymphoma monocyte) whole cell lysate at 20 µg
Lane 4:
HUVEC (human umbilical vein endothelial cell) whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Predicted band size: 58 kDa
Observed band size: 58 kDa
false
Related conjugates and formulations (1)
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Anti-ADA2 antibody [EPR25430-131]
Reactivity data
Product details
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
ADA2 plays an important role in modulating immune system activity and inflammation. Unlike its counterpart ADA1 ADA2 does not function as a monomer but as part of a larger protein complex. It participates in the maturation and differentiation of monocytes into macrophages and dendritic cells influencing both innate and adaptive immune responses. ADA2's functions suggest it has an effect on the vascular and immune system health.
Pathways
ADA2 holds a significant place in the adenosine signaling pathway where it regulates the balance between adenosine and inosine levels. This balance affects the extracellular signaling pathways that influence immune cell activity. ADA2 also interacts with other proteins in the inflammatory pathways notably influencing cytokine activity. Through these pathways it shows regulatory connections with proteins like CD39 and CD73 which also engage in purinergic signaling.
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