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. : LVIM026Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVIM026Z |
| Description | This lentivirus expresses human MYC under the control of EF1a promoter. It also contains RFP reporter gene and blasticidin 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(RFP, Bla) lentiviral particles are a cutting-edge tool for gene manipulation in mammalian cells. Genetically engineered, they enable efficient and flexible delivery of the human MYC oncogene. The EF1a promoter drives stable MYC gene expression, ensuring consistent protein levels across transduced cell populations. This lentiviral vector integrates two key selection markers: a red fluorescent protein (RFP) reporter gene for real-time monitoring of transduction efficiency via fluorescence microscopy or flow cytometry; and a blastcinidyl resistance gene (Bla) for stable selection of transduced cells in culture. The lentiviral platform itself offers significant advantages, including the ability to infect both dividing and non-dividing cells, long-term sustained transgene expression through genome integration, and broad tropism across multiple cell types.
The primary application of EF1a-hMYC(RFP, Bla) lentiviral particles is in cell immortalization, where overexpression of MYC can suppress senescence pathways, thereby extending the lifespan of primary cells or difficult-to-culture cell lines. This is of significant value for establishing stable cell models from patient-derived samples, primary epithelial cells, or stem cells (which have limited in vitro proliferative capacity). Researchers can rapidly generate immortalized cell lines by transducing target cells and subsequently screening for blastomycin; RFP markers immediately confirm successful transduction. Beyond immortalization, these particles facilitate MYC-focused tumorigenesis research, enabling the investigation of MYC-driven signaling pathways, metabolic reprogramming, and tumorigenesis in cancer models. The dual-selection markers also allow for synergistic experiments with other genetic elements or drug therapies. Furthermore, the resulting cell lines can serve as a stable platform for high-throughput drug screening, functional genomics, and disease modeling—particularly in areas where MYC dysregulation plays a pathophysiological role, such as oncology, regenerative medicine, and aging research.
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