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. : LVIM066Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVIM066Z |
| Description | This lentivirus expresses SV40 Large T Antigen under the control of EF1a promoter. It also contains Zeocin 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. |
EF1a-SV40/LTA(Zeo) Lentiviral Particles are high-titer, replication-incompetent viral vectors designed for the stable integration and expression of the Simian Virus 40 (SV40) Large T Antigen in mammalian cells. The expression is driven by the human Elongation Factor-1 alpha (EF1a) promoter, which provides high-level, constitutive transcriptional activity across a wide variety of cell types, including primary cells, stem cells, and hematopoietic lineages where other promoters might be prone to epigenetic silencing. The inclusion of the SV40 Large T Antigen (LTA) allows for the modulation of host cell cycle regulatory pathways, specifically through the inhibition of p53 and retinoblastoma (Rb) proteins. The vector also incorporates a Zeocin resistance gene as a selectable marker, enabling the rapid and precise generation of stable cell populations following transduction. These particles are typically concentrated and purified to ensure high efficiency and low cellular toxicity during the infection process.
These lentiviral particles are most commonly used for the immortalization of primary cells to establish continuous cell lines. By overriding natural senescence pathways, researchers can create stable models for long-term studies that would otherwise be impossible with finite primary cultures. This capability is essential in fields such as drug discovery, toxicology, and basic cell biology where a consistent cell supply is required. The SV40 Large T Antigen is also frequently utilized to enhance the expression of proteins in transient transfection systems. In cells expressing LTA, plasmids containing an SV40 origin of replication can undergo episomal amplification, leading to significantly higher yields of recombinant proteins or viral progeny. These particles also find utility in oncology research for studying transformation mechanisms, as well as in the development of specialized packaging cell lines for viral vector production. By providing a reliable method for stable LTA expression, these lentiviral particles facilitate the creation of robust experimental platforms for diverse molecular and cellular research needs.
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Particles were well-packaged and free of replication-competent virus (RCV). Transduction was efficient without causing excessive cytotoxicity, indicating high-quality lentiviral production.
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