Anti-CD39 antibody [EPR26473-58] (BSA and Azide free)
- BOND RX™ Validated
- RabMAb
- Recombinant
- What is this?
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(2 Reviews)
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- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD39 antibody [EPR26473-58] (BSA and Azide free) (AB300066)
This data was developed using ab300065, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human pancreas tissue labelling with ab300065 at 1/2000 (0.295 μg/ml) followed by a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection) was used. Positive staining on the endothelial cells and smooth muscle of human pancreas.The section was incubated with ab300065 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.
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-CD39 antibody [EPR26473-58] (BSA and Azide free) (AB300066)
This data was developed using ab300065, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human endometrial carcinoma tissue labelling CD39 with ab300065 at 1/2000 (0.295 μg/ml) followed by a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection) was used. Positive staining on the stromal cells of human endometrial carcinoma (PMID : 25403716).The section was incubated with ab300065 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.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CD39 antibody [EPR26473-58] (BSA and Azide free) (AB300066)
This data was developed using ab300065, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 80% Methanol-fixed, 0.1% TritonX-100 permeilized IM-9 (human multiple myeloma B Lymphoblast) cells lebelling CD39 with ab300065 at 1/50 (11.8 μg/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2μg/mL) dilution (Green). Confocal image showing membranous and cytoplasmic staining in IM-9 cell line. Negative control : Jurkat (PMID : 24319640). ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 (2.5μg/ml) dilution (Red). 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 (2μg/mL) dilution.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CD39 antibody [EPR26473-58] (BSA and Azide free) (AB300066)
This data was developed using ab300065, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 80% Methanol-fixed, 0.1% TritonX-100 permeilized Human PBMC cells lebelling CD39 with ab300065 at 1/50 (11.8 μg/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2μg/mL) dilution (Green). Confocal image showing membranous and cytoplasmic staining in human PBMC is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 (2.5μg/ml) dilution (Red). 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 μg/mL) dilution.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD39 antibody [EPR26473-58] (BSA and Azide free) (AB300066)
This data was developed using ab300065, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Human peripheral blood mononuclear cell (PBMC) cells labelling CD39 with ab300065 at 1/500 dilution (0.1μg)/ Right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control. Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody. Gated on viable cells. Cells were stained with rabbit IgG or ab300065. Then stained with anti-CD19 conjugated to Alexa Fluor®647.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD39 antibody [EPR26473-58] (BSA and Azide free) (AB300066)
This data was developed using ab300065, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human liver tissue labelling CD39 with ab300065 at 1/2000 (0.295 μg/ml) followed by a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection) was used. Positive staining on the endothelial cells and smooth muscle of human liver.The section was incubated with ab300065 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.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IP
Supplier Data
Immunoprecipitation - Anti-CD39 antibody [EPR26473-58] (BSA and Azide free) (AB300066)
This data was developed using ab300065, the same antibody clone in a different buffer formulation.
CD39 was immunoprecipitated from 0.35 mg Human placenta tissue lysate 10μg with ab300065 at 1/30 dilution (2μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab300065 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Human placenta tissue lysate 10μg
Lane 2 : ab300065 in Human placenta tissue lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab300065 in Human placenta tissue lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 10 seconds
All lanes:
Immunoprecipitation - Anti-CD39 antibody [EPR26473-58] (<a href='/en-us/products/primary-antibodies/cd39-antibody-epr26473-58-ab300065'>ab300065</a>)
Predicted band size: 58 kDa
false
- IP
Supplier Data
Immunoprecipitation - Anti-CD39 antibody [EPR26473-58] (BSA and Azide free) (AB300066)
This data was developed using ab300065, the same antibody clone in a different buffer formulation.
CD39 was immunoprecipitated from 0.35 mg Human heart tissue lysate 10μg with ab300065 at 1/30 dilution (2μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab300065 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Human heart tissue lysate 10μ
Lane 2 : ab300065 in Human heart tissue lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab300065 in Human heart tissue lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 67 seconds
All lanes:
Immunoprecipitation - Anti-CD39 antibody [EPR26473-58] (<a href='/en-us/products/primary-antibodies/cd39-antibody-epr26473-58-ab300065'>ab300065</a>)
Predicted band size: 58 kDa
false
- WB
Supplier Data
Western blot - Anti-CD39 antibody [EPR26473-58] (BSA and Azide free) (AB300066)
This data was developed using ab300065, the same antibody clone in different buffer formulation.
5% NFDM/TBST was used as blocking and diluting buffer.
Exposure time :
Lane 1 : 10 seconds
Lane 2 and 3 : 103 seconds
Negative control : Jurkat ( PMID : 9077545).
All lanes:
Western blot - Anti-CD39 antibody [EPR26473-58] (<a href='/en-us/products/primary-antibodies/cd39-antibody-epr26473-58-ab300065'>ab300065</a>) at 1/1000 dilution
Lane 1:
IM-9 (Human multiple myeloma B Lymphoblast) whole cell lysate at 20 µg
Lane 2:
THP-1 (Human monocytic leukemia monocyte) whole cell lysate at 20 µg
Lane 3:
Jurkat ( Human T cell leukemia T lymphocyte) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/50000 dilution
Predicted band size: 58 kDa
Observed band size: 78 kDa
false
- WB
Supplier Data
Western blot - Anti-CD39 antibody [EPR26473-58] (BSA and Azide free) (AB300066)
This data was developed using ab300065, the same antibody clone in different buffer formulation.
5% NFDM/TBST was used as blocking and diluting buffer.
Exposure time :
Lane 1:59 seconds
Lane 2:180 seconds
All lanes:
Western blot - Anti-CD39 antibody [EPR26473-58] (<a href='/en-us/products/primary-antibodies/cd39-antibody-epr26473-58-ab300065'>ab300065</a>) at 1/1000 dilution
Lane 1:
Human placenta tissue lysate at 20 µg
Lane 2:
Human heart tissue lysate at 20 µg
Secondary
All lanes:
Western blot - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/1000 dilution
Predicted band size: 58 kDa
Observed band size: 78 kDa
false
Related conjugates and formulations (3)
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Anti-CD39 antibody [EPR26473-58]
-
519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-CD39 antibody [EPR26473-58]
-
578 PE
PE Anti-CD39 antibody [EPR26473-58]
Reactivity data
Product details
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.
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.
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.
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Product protocols
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Target data
Alternative Names
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