38-1H2 is a specific antibody that binds precisely to two tandem VHH sequences of LCAR-B38M. These sequences are designed to target two epitopes of the B-cell maturation antigen (BCMA). BCMA is a protein expressed selectively by B-lineage cells, including both normal and malignant plasma cells in multiple myeloma. Ciltacabtagene autoleucel, also known as cilta-cel or Carvykti, is a gene-edited autologous CAR T-cell therapy. It utilizes LCAR and B38M to effectively recognize BCMA-positive cell
Item Information | |
Catalog # | 212002 |
Size/Concentration | 100 Tests |
Price | $550.00 |
Specification |
|
Host Species | Rabbit |
Antibody Type | Monoclonal |
Antibody Format |
Whole lgG |
Clone | 38-1H2 |
Immunogen |
two tandem VHH sequences of LCAR-B38M |
Conjugate |
Alexa Fluor 647 |
Excitation/Emission Ma |
651/667nm |
Storage Buffer |
Aqueous buffered solution containing protein stabilizer and ≤0.05% ProClin 30 |
Preparation and Storage
Shipping | The product is shipped at 2-8°C. |
Stability & Storage |
To provide optimal stability of reagent:
|
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-LCAR-B38M Monoclonal Antibody, 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-LCAR-B38M Monoclonal Antibody, 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.
References
1. Robert O. Carpenter et al., “B-Cell Maturation Antigen Is a Promising Target for Adoptive T-Cell Therapy of Multiple Myeloma,” Clinical Cancer
Research 19, no. 8 (April 15, 2013): 2048–60, https://doi.org/10.1158/1078-0432.CCR-12-2422.
2. Bo Yu, et al., “BCMA-Targeted Immunotherapy for Multiple Myeloma,” Journal of Hematology & Oncology 13, no. 1 (December 2020): 125,
https://doi.org/10.1186/s13045-020-00962-7
Flow Cytometry Protocol
Required Materials
- Rabbit Anti-LCAR-B38M Monoclonal Antibody, Alexa Fluor 647
- Dead Cell Staining Solution
- Additional Fluorochrome-Conjugated Antibodies (as required)
- Red Blood Cell Lysis Solution
- FACS Buffer (PBS containing 2% BSA)
- Anticoagulated Whole Blood or Cell Samples
Protocol for Whole Blood Samples
-
Reagent Addition
- Add 1 μL of Rabbit Anti-LCAR-B38M Monoclonal Antibody, Alexa Fluor 647 to the tube.
- Include dead cell staining solution and any additional fluorochrome-conjugated antibodies as needed.
-
Whole Blood Addition and Mixing
- Pipette 100 μL of well-mixed, anticoagulated whole blood into the tube. Ensure thorough mixing to avoid sample smearing on the tube sides, which could result in incomplete staining.
-
Incubation
- Incubate for 25 minutes in the dark at room temperature (18-25°C) to allow binding.
-
RBC Lysis
- Add Red Blood Cell Lysis Solution, mix gently yet thoroughly, and incubate for 15 minutes in the dark at room temperature.
-
Washing
- Add 500 μL of FACS buffer, mix, and centrifuge at 300g for 5 minutes at room temperature. Aspirate the supernatant completely.
- Repeat this washing step twice for thorough removal of unbound reagents.
-
Resuspension and Flow Cytometry
- 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, then count and assess viability.
-
Cell Suspension
- Adjust the cell suspension to a concentration of up to 1×10^6 nucleated cells per 100 μL of FACS buffer.
-
Antibody and Reagent Addition
- Add 1 μL of Rabbit Anti-LCAR-B38M Monoclonal Antibody, 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 step twice to ensure removal of unbound reagents.
-
Resuspension and Flow Cytometry
- Resuspend cells in an appropriate volume of FACS buffer for analysis by flow cytometry.
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