Rabbit Recombinant Monoclonal Mesothelin antibody. Carrier free. Suitable for IP, WB, IHC-P and reacts with Mouse samples.
pH: 7.2 - 7.4
Constituents: PBS
IP | WB | IHC-P | |
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Mouse | Tested | Tested | Tested |
Species | Dilution info | Notes |
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Species Mouse | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Mouse | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Mouse | Dilution info 1/500 | Notes - |
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Membrane-anchored forms may play a role in cellular adhesion. Megakaryocyte-potentiating factor (MPF) may potentiate megakaryocyte colony formation.
Mes, Mpf, Msln, Mesothelin, Pre-pro-megakaryocyte-potentiating factor
Rabbit Recombinant Monoclonal Mesothelin antibody. Carrier free. Suitable for IP, WB, IHC-P and reacts with Mouse samples.
pH: 7.2 - 7.4
Constituents: PBS
This antibody recognizes a different epitope of Mesothelin compared to ab187063.
ab232219 is the carrier-free version of Anti-Mesothelin antibody [EPR17823-69] ab213174.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
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 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
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.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
Mesothelin was immunoprecipitated from 1 mg NIH/3T3 (mouse embryo fibroblast cell line) whole cell lysate with Anti-Mesothelin antibody [EPR17823-69] ab213174 at 1/40 dilution. Western blot was performed from the immunoprecipitate using Anti-Mesothelin antibody [EPR17823-69] ab213174 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366), was used for detection at 1/10000 dilution.
Lane 1: NIH/3T3 whole cell lysate 10 μg (Input).
Lane 2: Anti-Mesothelin antibody [EPR17823-69] ab213174 IP NIH/3T3 whole cell lysate (+).
Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-Mesothelin antibody [EPR17823-69] ab213174 in NIH/3T3 whole cell lysate (-)
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 3 seconds.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Mesothelin antibody [EPR17823-69] ab213174).
All lanes: Immunoprecipitation - Anti-Mesothelin antibody [EPR17823-69] (Anti-Mesothelin antibody [EPR17823-69] ab213174)
Predicted band size: 69 kDa
Observed band size: 40 kDa, 70 kDa
Exposure time: 3s
Blocking and dilution buffer: 5% NFDM /TBST.
The expression profile observed is consistent with what has been described in the literature (PMID: 16857795; PMID: 17332303).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Mesothelin antibody [EPR17823-69] ab213174).
All lanes: Western blot - Anti-Mesothelin antibody [EPR17823-69] (Anti-Mesothelin antibody [EPR17823-69] ab213174) at 1/1000 dilution
Lane 1: NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 10 µg
Lane 2: Mouse lung lysate at 10 µg
All lanes: Goat Anti-Rabbit IgG Peroxidase Conjugate, specific to the non-reduced form of IgG at 1/10000 dilution
Developed using the ECL technique.
Predicted band size: 69 kDa
Observed band size: 40 kDa, 71 kDa
Exposure time: 3min
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Mesothelin antibody [EPR17823-69] ab213174).
Immunohistochemical analysis of paraffin-embedded mouse lung labelling Mesothelin with Anti-Mesothelin antibody [EPR17823-69] ab213174 at 1/500 dilution, followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP).
Positive staining on mesothelium of mouse lung.
The section was incubated with Anti-Mesothelin antibody [EPR17823-69] ab213174 at 4°C overnight.
Counterstained with Hematoxylin.
Heat mediated antigen retrieval was performed using Antigen Retrieval Buffer (100X Tris-EDTA Buffer, pH 9.0) ab93684 (Tris/EDTA buffer, pH 9.0).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Mesothelin antibody [EPR17823-69] ab213174).
Immunohistochemical analysis of paraffin-embedded mouse spleen labelling Mesothelin with Anti-Mesothelin antibody [EPR17823-69] ab213174 at 1/500 dilution, followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP).
Positive staining on mesothelium of mouse spleen.
The section was incubated with Anti-Mesothelin antibody [EPR17823-69] ab213174 at 4°C overnight.
Counterstained with Hematoxylin.
Heat mediated antigen retrieval was performed using Antigen Retrieval Buffer (100X Tris-EDTA Buffer, pH 9.0) ab93684 (Tris/EDTA buffer, pH 9.0).
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