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. : LVIM051Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVIM051Z |
| Description | This lentivirus expresses SV40 Large T Antigen under the control of CMV promoter. It also contains GFP reporter gene and 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(GFP, Bla) lentiviral particles are cutting-edge tools in gene manipulation and cell engineering. These genetically engineered particles deliver the SV40 large T antigen (LTA) gene under the control of a potent CMV promoter, ensuring high levels of constitutive expression in transduced cells. A key advantage of this lentiviral system lies in its dual-function design: it integrates a GFP reporter gene for real-time visualization of transduction efficiency and cell localization, and also integrates a blastcin resistance gene (Bla) to facilitate screening for stably transduced cells via antibiotics. Furthermore, the lentiviral vector backbone offers other advantages, such as efficient integration into both dividing and non-dividing cells, broad tropism across various mammalian cell types, and stable long-term transgenic expression—all of which outperform transient transfection methods.
This multifunctional lentiviral system is particularly important in cell immortalization research. SV40 LTA can inactivate tumor suppressor pathways (such as p53 and Rb), thereby promoting the generation of proliferating cell lines from finite-lived primary tissues. These immortalized cells retain key physiological characteristics, enabling long-term experiments such as drug screening, toxicology assessment, and cellular pathway mechanism studies—experiments impossible in senescent primary cells. In addition to immortalization, these viral particles also support gene function analysis in difficult-to-transfect cells (such as neurons or stem cells), the construction of reporter gene cell lines for high-content screening, and the creation of disease models (where sustained LTA expression mimics oncogenic transformation).
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The viral titer was accurate, and we observed no contamination issues. The particles were potent, and even low MOIs gave us satisfactory results.
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