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. : LVG00083Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00083Z |
| Description | Lentivirus particles containing luciferase reporter gene under the control of a minimal promoter and beta-Catenin/Wnt TCF-LEF 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 Wnt/β-catenin/TCF-LEF Luciferase Reporter Lentivirus offers a powerful tool for studying Wnt signaling pathway activity, featuring high-titer lentiviral particles that ensure efficient and stable transduction of both dividing and non-dividing cells. This system contains a firefly luciferase reporter gene driven by a minimal promoter coupled with multiple TCF/LEF response elements, enabling sensitive detection of β-catenin-mediated transcriptional activity. The lentiviral vector provides distinct advantages, including long-term stable expression through genomic integration, broad cellular tropism, and the ability to establish reporter cell lines with consistent responsiveness. Compared to transient transfection methods, this lentiviral approach yields more reproducible results with lower inter-experimental variability.
This reporter system has become indispensable for both basic research and drug discovery applications involving the Wnt pathway. Researchers routinely employ it to monitor Wnt/β-catenin signaling activation in diverse experimental settings, including stem cell differentiation studies, cancer research (particularly in colorectal and hepatocellular carcinomas), and developmental biology investigations. Pharmaceutical scientists utilize this tool for high-throughput screening of Wnt pathway modulators, evaluating both agonists and inhibitors. The system proves particularly valuable for studying crosstalk between Wnt signaling and other pathways, identifying novel pathway components through functional genomics approaches, and validating therapeutic targets.
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We were impressed by the consistency of the reporter virus in multiple experiments. The product reliably produced robust luminescent signals across different experimental setups, making it a dependable tool for our signaling studies.
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