The rabbit monoclonal antibody R2L specifically binds to the scFv region of a CD19-specific mouse monoclonal antibody (mAb, clone FMC63). CD19 antigen is a B-cell specific cell surface antigen, which is expressed in all B-cell lineage malignancies and normal B-cells. The scFv region of FMC63 has been used to develop CD19-specific chimeric antigen receptor (CAR) T cells utilized in clinical trials.
Item Information | |
Catalog # | 203401 |
Size/Concentration | 25 tests |
Price | $530.00 |
Specification | |
Host Species | Rabbit |
Antibody Type | Monoclonal |
Antibody Format |
Whole IgG |
Reactivity | Mouse |
Immunogen | scFv region of a CD19-specific mouse mAb clone FMC |
Storage Buffer | Aqueouus buffered solution containing protein stabilizer and ≤0.05% ProClin 300 |
Conjugate |
Alexa Fluor 647 |
Preparation & Storage
- Store undiluted at 2-8°C.
- Avoid prolonged exposure to light.
- Avoid freeze/thaw cycle of the reagent.
- The monoclonal antibody was purified by Protein A.
- The antibody was conjugated with PE under optimum conditions, and unincorporated dye was removed
FACS Protocol
BioSwan reagents can be used with or without an isotype control to assess the amount of nonspecific antibody binding.
(Optional) For Whole Blood Sample
1. Pipette 1 μL Rabbit Anti-Mouse FMC63 scFv Monoclonal Antibody (R2L), Alexa Fluor 647 into the bottom of the tube.
2. Add dead cell staining solution and additional fluorochrome conjugated antibodies into the bottom of the tube.
3. Pipette 100 μL of well-mixed, anticoagulated whole blood into the bottom of the tube. Mix gently and thoroughly.
Note Avoid smearing sample down the side of the tube. If the sample remains on the side of the tube, it will not be stained with the reagents.
4. Incubate for 25 minutes in the dark at room temperature (18-25°C).
5. Pipette Red Blood Cell Lysis Solution to the tube. Mix gently and thoroughly. Incubate for 15 minutes in the dark at room temperature (18-25°C).
6. Add 500 μL FACS buffer to the tube. Mix well and centrifuge at 300g for 5 minutes at room temperature (18-25°C). Aspirate supernatant
completely.
7. Repeat step 6 twice.
8. Add a suitable amount of FACS buffer to resuspend cell and analysis by flow cytometry.
(Optional) For Cell Sample
1. Harvest the cells and wash the cells twice by FACS buffer.
2. Count the cells number and the viability.
3. Resuspend the cell suspension to a concentration up to 1×106 nucleated cells per 100 μL of buffer.
4. Add 1 μL Rabbit Anti-Mouse FMC63 scFv Monoclonal Antibody (R2L), Alexa Fluor 647, dead cell staining solution and additional fluorochrome. Mix gently and thoroughly.
5. Incubate for 25 minutes in the dark at room temperature (18-25°C).
6. Add 500 μL FACS buffer to the tube. Mix well and centrifuge at 300 g for 5 minutes at room temperature (18-25°C). Aspirate supernatant completely.
7. Repeat step 6 twice.
8. Add a suitable amount of FACS buffer to resuspend cell and analysis by flow cytometry.
Product Notices
1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
2. Caution: Antibody solutions containing ProClin 300 should be handled with care. Do not take internally and avoid all contact with the skin, mucosa and eyes.
Intellectual Product Notices
1. This product is provided under an intellectual property license from Life Technologies Corporation. The transfer of this product is conditioned on the buyer using the purchased product solely in research conducted by the buyer and the buyer must not (1) use this product or its components
for (a) diagnostic, therapeutic or prophylactic purposes; or (b) manufacturing or quality assurance or quality control, and/or (2) sell or transfer this product or its components for resale, whether or not resold for use in research. For information on purchasing a license to this product for purposes other than as described above, contact Life Technologies Corporation, 5781 Van Allen Way, Carlsbad, CA 92008 USA or outlicensing@thermofisher.com.
2. Conditions: The information disclosed herein is not to be construed as a recommendation to use the above product in violation of any patents.
BioSwan will not be held responsible for patent infringement or other violations that may occur with the use of our products. Purchase does not
include or carry any right to resell or transfer this product either as a stand-alone product or as a component of another product. Any use of this product other than the permitted use without the express written authorization of BioSwan Company is strictly prohibited.
For Research Use Only. Not for use in diagnostic or therapeutic procedures. Not for resales. BioSwan, the BioSwan Logo and all other trademarks are property of BioSwan Laboratories, Co., Ltd.
Flow Cytometry Protocol
Required Reagents
- Rabbit Anti-Mouse FMC63 scFv Monoclonal Antibody (R2L), Alexa Fluor 647
- Dead Cell Staining Solution
- Additional Fluorochrome-Conjugated Antibodies
- Red Blood Cell Lysis Solution
- FACS Buffer (PBS containing 2% BSA)
- Anticoagulated Whole Blood or Cell Samples
Protocol for Whole Blood Samples
-
Antibody and Reagent Addition
- Add 1 μL of Rabbit Anti-Mouse FMC63 scFv Monoclonal Antibody (R2L), Alexa Fluor 647 into a tube.
- Incorporate dead cell staining solution and any other necessary fluorochrome-conjugated antibodies.
-
Whole Blood Addition and Mixing
- Pipette 100 μL of well-mixed, anticoagulated whole blood into the tube, ensuring gentle and thorough mixing to avoid smearing the sample on the tube’s sides.
-
Incubation
- Incubate the mixture for 25 minutes in the dark at room temperature (18-25°C).
-
RBC Lysis
- Add Red Blood Cell Lysis Solution, mix gently and thoroughly, and incubate for 15 minutes in the dark at room temperature.
-
Washing
- Add 500 μL of FACS buffer to the tube, mix well, and centrifuge at 300g for 5 minutes at room temperature. Completely aspirate the supernatant.
- Repeat the wash step twice to ensure thorough removal of unbound reagents.
-
Resuspension and Flow Cytometry Analysis
- Resuspend the cells in a suitable volume of FACS buffer and proceed to flow cytometry analysis.
Protocol for Cell Samples
-
Cell Preparation
- Harvest and wash cells twice with FACS buffer. Perform cell counting and viability assessment.
-
Cell Suspension
- Adjust the cell suspension to a concentration of up to 1×10^6 nucleated cells per 100 μL of buffer.
-
Antibody and Reagent Addition
- Add 1 μL of Rabbit Anti-Mouse FMC63 scFv Monoclonal Antibody (R2L), Alexa Fluor 647, along with dead cell staining solution and any additional fluorochromes. Mix gently and thoroughly.
-
Incubation
- Incubate for 25 minutes in the dark at room temperature (18-25°C).
-
Washing
- Add 500 μL of FACS buffer, mix well, and centrifuge at 300g for 5 minutes at room temperature. Aspirate the supernatant completely.
- Repeat this wash step twice to ensure the removal of unbound reagents.
-
Resuspension and Flow Cytometry Analysis
- Resuspend the cells in an appropriate volume of FACS buffer and analyze by flow cytometry.
Notes
- The use of isotype controls is recommended for accurately assessing nonspecific binding, especially when establishing new antibody panels or experimental conditions.
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