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. : LVIM025Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVIM025Z |
| Description | This lentivirus expresses human MYC under the control of EF1a promoter. It also contains GFP reporter gene and puromycin resistance gene for selection. This virus can be used for cell immortalization. |
| Gene | MYC |
| 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. |
| Target Gene | MYC |
| Background | This gene encodes human lysozyme, whose natural substrate is the bacterial cell wall peptidoglycan (cleaving the beta[1-4]glycosidic linkages between N-acetylmuramic acid and N-acetylglucosamine). Lysozyme is one of the antimicrobial agents found in human milk, and is also present in spleen, lung, kidney, white blood cells, plasma, saliva, and tears. The protein has antibacterial activity against a number of bacterial species. Missense mutations in this gene have been identified in heritable renal amyloidosis. [provided by RefSeq, Oct 2014] |
EF1a-hMYC(GFP, Puro) lentiviral particles represent a cutting-edge tool for gene manipulation in cell biology research. This genetically engineered lentiviral vector system expresses the human MYC oncogene under the control of a highly efficient EF1a promoter, ensuring stable and sustained expression in transduced cells. The vector integrates two key selection markers: a GFP reporter gene for real-time visualization of transduction efficiency and cell localization; and a puromycin resistance gene for rapid and stable screening of successfully transduced cells. Utilizing lentiviral delivery technology, the system achieves high transduction efficiency in both dividing and non-dividing cell types, and stable genome integration enables long-term transgene expression. Its self-inactivation (SIN) design minimizes the risk of insertional mutations while maintaining robust promoter activity.
This lentiviral particle system is particularly important in cell immortalization research because sustained MYC expression can bypass the senescence mechanisms of primary cells. By extending the replication life of previously short-lived cell cultures, researchers can establish stable cell lines for long-term experiments in cancer biology, regenerative medicine, and drug discovery platforms. The GFP reporter gene allows for non-invasive monitoring of transduction success rate and transgene expression dynamics via fluorescence microscopy or flow cytometry, while puromycin screening ensures cell population homogeneity by removing untransduced cells. The system's applications extend to functional genomics research, exploring the role of MYC in cell cycle regulation, apoptosis resistance, metabolic reprogramming, and stem cell maintenance. Furthermore, the system facilitates the development of disease models for tumorigenesis research and provides a platform for screening therapeutics targeting the MYC-driven pathway.
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From purchase to data, it took only two weeks. The virus is highly active, allowing for immediate, stress-free experimentation, helping to rapidly advance research.
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