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. : LVG00110Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00110Z |
| Description | Lentivirus particles containing luciferase reporter gene under the control of a minimal promoter and Nanog response element. |
| 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 Nanog luciferase reporter lentivirus is a ready-to-use, replication-deficient lentiviral vector engineered to convert Nanog pathway activity into a sensitive luminescent signal. This vector places the firefly luciferase reporter gene under the control of a minimal promoter containing multiple Nanog response elements, resulting in very low background signal and a wide dynamic range upon pathway activation. Because the reporter gene integrates into the host genome, it supports stable, long-term expression during cell division, making it ideal for long-term studies without the need for repeated transfections. Broad host tropism pseudotyping technology enables efficient transduction of a wide variety of human and murine cell types, including stem cells and difficult-to-transfect cell lines. Furthermore, the vector incorporates typical lentiviral backbone optimizations to promote high expression, high integration efficiency, and genetic stability.
This reporter gene is broadly applicable to any field requiring quantitative, real-time analysis of Nanog pathway dynamics. In pluripotent stem cell research, it can continuously monitor the self-renewal status of cells, helping to optimize culture conditions and media formulations for maintaining or regulating pluripotency. During cell reprogramming, the reporter gene can dynamically reflect Nanog activation kinetics, assisting researchers in comparing different reprogramming protocols, evaluating donor cell sources, and characterizing the transition from partially reprogrammed to fully reprogrammed states. In directed differentiation, it can serve as an early indicator of pluripotency loss and help benchmark lineage differentiation protocols.
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We successfully transduced THP-1 and RAW264.7 cells with high efficiency. The virus integrates well and maintains stable expression.
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