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. : LVIM050Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVIM050Z |
| Description | This lentivirus expresses SV40 Large T Antigen under the control of CMV promoter. It also contains blasticidin resistance gene for selection. This virus can be used for cell immortalization. |
| Gene | SV40 Large T Antigen |
| 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. |
CMV-SV40/LTA (Bla) lentiviral particles are sophisticated tools for gene manipulation and cell engineering, designed to efficiently deliver the SV40 large T antigen (LTA) gene to target cells. This lentiviral vector system utilizes a robust cytomegalovirus (CMV) promoter, ensuring stable expression of the SV40 LTA transgene in a variety of mammalian cell types. The introduced blast fungicide resistance gene (Bla) provides an effective screening mechanism, enabling researchers to enrich stably transduced cells under blast fungicide treatment. HIV-1-derived lentiviral vectors offer numerous inherent advantages, including the ability to transduce both dividing and non-dividing cells, long-term transgene expression through genome integration, and good safety due to their self-inactivation (SIN) design. The high titers achievable with these particles further enhance their application value, enabling efficient gene delivery even in difficult-to-transduce cell types such as primary cells or stem cells.
The primary application of these lentiviral particles is in cell immortalization, a key technology for extending the lifespan of primary cells that otherwise age after a limited number of passages in vitro. The SV40 large T antigen is a potent oncoprotein that inactivates key tumor suppressor proteins such as p53 and retinoblastoma protein (pRb), thereby bypassing cellular senescence checkpoints and achieving unlimited proliferation. This immortalization capability is crucial for constructing stable cell lines from tissues that are difficult to culture long-term, such as human epithelial cells, fibroblasts, and specialized cell types like hepatocytes or neurons. These immortalized cells retain many physiological characteristics of their primary cells, making them ideal models for studying disease mechanisms, drug screening, toxicological assessments, and molecular signaling pathways. In addition to immortalization, lentiviral particles can also be used in functional genomics research to explore the role of SV40 LTA in cell transformation, DNA replication, and viral pathogenesis.
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Following the recommended protocol, we achieved high transduction rates with minimal optimization. The immortalized cells have been growing stably for months—great product!
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