Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : LVG00007Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00007Z |
| Description | Lentivirus particles containing first generation of anti-CD20 CAR (chimeric antigen receptor) scFv-CD3zeta. |
| Gene | MS4A1 |
| Titer | Varies lot by lot, for example, ≥1*10^7 TU/mL, ≥1*10^8 TU/mL, ≥1*10^9 TU/mL etc. |
| Size | Varies lot by lot, for example, 100 ul, 500 ul, 1 mL etc. |
| Storage | Store at -80℃. Avoid multiple freeze/thaw cycles. |
| Shipping | Frozen on dry ice |
| Summary | Creative Biogene ensures high-quality lentivirus particles by optimizing and standardizing production protocols and performing stringent quality control (QC). The specific QC experiments performed vary between lentivirus particle lots. |
| Mycoplasma | Creative Biogene routinely tests for mycoplasma contamination using a mycoplasma detection kit. Cell lines are maintained for approximately 20 passages before being discarded and replaced with a new vial of early passage cells. Approximately 2 weeks after thawing, cell culture supernatants are tested for mycoplasma contamination. Creative Biogene ensures that lentiviral products are free of mycoplasma contamination. |
| Purity | Creative Biogene evaluates the level of impurities, such as residual host cell DNA or proteins, in prepared lentiviral vectors to ensure they meet quality standards. |
| Sterility | The lentiviral samples were inoculated into cell culture medium for about 5 days and the growth of bacteria and fungi was tested. Creative Biogene ensures that the lentiviral products are free of microbial contamination. |
| Transducibility | Upon requirement, Creative Biogene can perform in vitro or in vivo transduction assays to evaluate the ability of lentivirus to deliver genetic material into target cells, and assess gene expression and functional activities. |
| Proviral Identity Confirmation | All Creative Biogene lentiviral vectors are confirmed to have correctly integrated provirus using PCR. This test involves transducing cells with serial dilutions of the lentiviral vector, harvesting the cells a few days later, and isolating genomic DNA. This DNA is then used as a template to amplify a portion of the expected lentiviral insert. |
| Gene Name | MS4A1 membrane-spanning 4-domains, subfamily A, member 1 [ Homo sapiens ] |
| Gene Symbol | MS4A1 |
| Synonyms | B1; S7; Bp35; CD20; CVID5; MS4A2; LEU-16 |
| Gene Description | membrane-spanning 4-domains, subfamily A, member 1 |
| Gene ID | 931 |
| Uni Prot ID | P11836 |
| m RNA Refseq | NM_021950.3 |
| Protein Refseq | NP_068769.2 |
| Chromosome Location | 11q12 |
| Pathway | Hematopoietic cell lineage, organism-specific biosystem; Hematopoietic cell lineage, conserved biosystem; |
| MIM | 112210 |
The scFv(CD20)-CD3zeta CAR-T lentivirus is a research-grade lentiviral particle preparation designed to deliver a first-generation anti-CD20 chimeric antigen receptor (CAR), which is composed of a CD20-specific single-chain variable fragment (scFv) fused to a CD3ζ signaling domain. This vector is constructed on a modern, safety-engineered lentiviral backbone, supporting durable genomic integration and long-term expression in human T cells, enabling sustained CAR expression on the cell surface for long-term functional assessment. The platform emphasizes high functional consistency, reliable gene delivery to primary cells, and reduced risk of promoter silencing, supporting reproducible experiments at multiple time points.
This lentiviral product is suitable for a wide range of applications in the field of CD20-targeted immunotherapy, including drug discovery, preclinical research, and translational method development. It supports in vitro modeling of CD20-expressing B-cell malignancies, including studies of diseases such as non-Hodgkin lymphoma, chronic lymphocytic leukemia, and mantle cell lymphoma. Researchers can utilize this system to assess the impact of antigen density dependence, epitope accessibility, and microenvironmental factors on CAR function, enabling hypothesis-driven comparisons across different cell states, tumor models, and co-stimulatory pathways. Furthermore, it can be integrated into target validation, off-target risk assessment in normal B cell subsets, and exploratory safety pharmacology platforms, providing a basis for rational design choices for subsequent constructs. In vivo, this tool can be used for fundamental modeling of antitumor activity and persistence in appropriate animal models, helping to assess exposure-response relationships and resistance mechanisms.
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Lentivirus titer was higher than claimed! Achieved >90% transduction efficiency in primary T-cells without optimization. Critical for our time-sensitive immunotherapy project.
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