For research use only
| Cat No. | ABC-RC023Y |
| Product Type | Reporter Stable Cell Lines |
| Cell Type | B Lymphocyte |
| Species | Human |
| Host Cell | RPMI-8226 |
| Source Organ | Peripheral Blood |
| Disease | Myeloma |
| Storage | Liquid Nitrogen |
BCMA Knockout RPMI-8226/Luciferase Cell Line by AcceGen enables dual-mode myeloma studies with BCMA signaling research and bioluminescent tumor tracking.
BCMA Knockout RPMI-8226/Luciferase Cell Line is a human multiple myeloma model generated from RPMI-8226 cells using CRISPR/Cas9-mediated knockout of BCMA (B-cell maturation antigen) combined with stable luciferase reporter integration. This dual-modified line maintains plasma cell morphology and characteristic markers (CD38, CD138), while enabling highly sensitive, non-invasive tumor tracking through bioluminescence imaging. It serves as a critical negative control for evaluating BCMA-targeted therapies such as CAR-T and antibody-drug conjugates, while supporting research into BCMA-independent signaling and resistance pathways. Suitable for in vitro assays and in vivo tumor modeling, this line provides a robust tool for preclinical drug screening and mechanism studies. All cells are cryopreserved at low passage (<P20) and rigorously tested free of HIV-1, HBV, HCV, syphilis, mycoplasma, fungi, yeast, and bacteria.
| Species | Human |
| Cat.No | ABC-RC023Y |
| Product Category | Transfected Stable Cell Lines |
| Size/Quantity | 1 vial |
| Cell Type | B Lymphocyte |
| Growth Mode | Suspension |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Peripheral Blood |
| Disease | Myeloma |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Reporter Stable Cell Lines |
| Host Cell | RPMI-8226 |
| Gene Info | BCMA Knockout / Luciferase |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
BCMA Knockout RPMI-8226/Luciferase Cell Line enables sensitive monitoring of tumor dynamics in BCMA-targeting therapy development. The bioluminescent reporter allows quantitative assessment of tumor growth and drug response in vivo, while the BCMA knockout provides a critical control for validating target specificity of immunotherapies. Ideal for studying BCMA-independent resistance mechanisms and evaluating next-generation myeloma treatments.