The rabbit monoclonal antibody 1F5 specifically binds to the scFv region of a CD20-specific human monoclonal antibody (mAb, clone 2C6). CD20 (cluster of differentiate 20) is a protein that is expressed on the surface of B cells, starting at the pre-B cell stage and also on mature B cells in the bone marrow and in the periphery. CD20 is not expressed on hematopoietic stem cells, pro-B cells, or normal plasma cells. The scFv region of 2C6 has been used to develop CD20-specific chimeric antigen receptor (CAR) T cells utilized in clinical trials.
Item Information |
|
Catalog # | 202405 |
Size/Concentration | 25 tests |
Price | $480.00 |
Specification |
|
Host Species | Rabbit |
Antibody Type | Monoclonal |
Antibody Format |
Whole IgG |
Reactivity | Human |
Immunogen | scFv region of a CD20-specific Human mAb clone 2C6 |
Storage Buffer | Aqueouus buffered solution containing protein stabilizer and ≤0.05% ProClin 300 |
Conjugate |
PE |
Preparation & Storage
- Store undiluted at 2-8°C.
- Avoid prolonged exposure to light.
- 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-Human 2C6 scFv Monoclonal Antibody, PE 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-Human 2C6 scFv Monoclonal Antibody, PE, 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. 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-Human 2C6 scFv Monoclonal Antibody, PE
- Dead Cell Staining Solution
- Additional Fluorochrome-Conjugated Antibodies (optional)
- Red Blood Cell Lysis Solution
- FACS Buffer (PBS with 2% BSA)
- Anticoagulated Whole Blood or Cell Samples
Protocol for Whole Blood Samples
-
Initial Reagent Addition
- Add 1 μL of Rabbit Anti-Human 2C6 scFv Monoclonal Antibody, PE to the tube.
- Introduce dead cell staining solution and any other fluorochrome-conjugated antibodies required.
-
Sample Addition and Mixing
- Pipette 100 μL of well-mixed, anticoagulated whole blood into the tube, ensuring gentle and thorough mixing to prevent sample smearing on tube sides.
-
Incubation
- Incubate for 25 minutes in the dark at room temperature (18-25°C).
-
Red Blood Cell Lysis
- Add Red Blood Cell Lysis Solution, mix gently and thoroughly, then incubate for 15 minutes in the dark at room temperature.
-
Washing
- Add 500 μL FACS buffer, mix, centrifuge at 300g for 5 minutes at room temperature, and completely aspirate the supernatant.
- Repeat this step twice to ensure thorough removal of unbound reagents.
-
Resuspension and Analysis
- Resuspend 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. Count cells and assess viability.
-
Cell Suspension Adjustment
- Adjust cell suspension to a concentration of up to 1×10^6 nucleated cells per 100 μL of buffer.
-
Reagent Addition
- Add 1 μL of Rabbit Anti-Human 2C6 scFv Monoclonal Antibody, PE, 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 FACS buffer, mix well, and centrifuge at 300g for 5 minutes at room temperature. Aspirate the supernatant completely.
- Repeat this washing step twice.
-
Final Resuspension and Flow Cytometry
- Resuspend cells in an appropriate volume of FACS buffer for flow cytometry analysis.
Notes
- The inclusion of isotype controls is recommended, especially when establishing new staining panels or experimental conditions, to provide insights into nonspecific binding levels.
Tabd 1 Content