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. : LVIM059Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVIM059Z |
| Description | This lentivirus expresses SV40 Large T Antigen under the control of EF1a 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. |
The EF1a-SV40/LTA(Bla) Lentiviral Particles represent a specialized genetic tool designed for the robust and stable expression of the Simian Virus 40 Large T Antigen (SV40 LTA) in mammalian systems. This lentiviral vector utilizes the human elongation factor 1 alpha (EF1a) promoter, which is highly valued for its ability to drive strong, constitutive transgene expression across a wide variety of cell types, including primary, stem, and progenitor cells where other promoters might face silencing. The SV40 LTA itself is a potent viral oncoprotein that functions by inactivating key host tumor suppressor proteins, specifically p53 and the retinoblastoma (pRb) family, thereby promoting continuous cell cycle progression. To ensure the reliability of experimental outcomes, the particles incorporate a blasticidin resistance gene (Bla), which serves as a selectable marker for the rapid isolation of successfully transduced cells. This third-generation, replication-deficient system is engineered for high biosafety and efficient integration into the host genome, providing a permanent genetic modification solution.
The primary application of these lentiviral particles is the immortalization of primary cell lines, allowing researchers to extend the proliferative lifespan of cells that would otherwise undergo senescence. By bypassing natural cell cycle checkpoints, the SV40 LTA enables the creation of stable, long-term cell models from finite clinical or primary tissue samples. Beyond immortalization, these particles are extensively utilized in molecular biology to investigate the mechanisms of viral oncogenesis, DNA replication, and cellular transformation. The use of a lentiviral delivery system is particularly advantageous for hard-to-transfect cell populations, ensuring high transduction efficiency and uniform expression within the culture. Additionally, the blasticidin selection marker streamlines the generation of stable cell pools, making this tool indispensable for high-throughput screening, protein production assays, and functional genomics studies where consistent protein expression is required over multiple passages.
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The performance of this lentiviral system exceeded our expectations. It provided a reliable option for our cell line development projects.
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