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. : LVG00116Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00116Z |
| Description | Lentivirus particles containing luciferase reporter gene under the control of a minimal promoter and Oct4 response element. |
| Gene | Oct4-Luc |
| 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 Oct4 luciferase reporter lentiviral vector provides a sensitive, specific, and stable readout of Oct4 pathway transcriptional activity, enabling real-time monitoring of pluripotency network dynamics in living cells. Its core design places the luciferase reporter gene under the control of tandem Oct4 response elements upstream of a minimal promoter, ensuring minimal background leakage while maximizing responsiveness to endogenous Oct4 transcriptional activation. The lentiviral vector format supports efficient gene delivery into dividing and non-dividing mammalian cells and achieves genomic integration for sustained expression, making it suitable for long-term studies and clonal tracking without repeated transfection.
In the field of stem cell biology, the Oct4 luciferase reporter lentiviral vector can be used to monitor pluripotency maintenance, detect early loss of pluripotency identity, and evaluate differentiation protocols that downregulate core stem cell factors. During cellular reprogramming to induced pluripotent stem cells, this reporter gene serves as a sensitive indicator of successful transcriptional activation of the endogenous pluripotency network, allowing for comparative evaluation of factor combinations, delivery methods, and culture protocols. In drug discovery and chemical biology, it provides a reliable and easily quantifiable readout for high-throughput or high-content screening of small molecules, biologics, or genetic perturbations that modulate Oct4 signaling, suitable for dose-response and kinetic analyses.
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Shipping was prompt, and the virus titer was as specified. We saw strong expression within 48 hours post-transduction. No need for additional concentration—ready to use!
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