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. : LVG00096Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00096Z |
| Description | Lentivirus particles containing luciferase reporter gene under the control of a minimal promoter and Hedgehog Gli 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 Hedgehog-Gli luciferase reporter lentivirus is a powerful tool for studying the Hedgehog (Hh) signaling pathway, which plays a crucial role in embryonic development and tissue homeostasis. These lentiviral particles contain a luciferase reporter gene driven by a minimal promoter and coupled to Hedgehog Gli response elements, enabling sensitive and quantitative detection of Hh pathway activity. This lentiviral vector system offers several significant advantages: stable integration into both dividing and non-dividing cells, ensuring long-term expression of the reporter gene; and high transduction efficiency, making it suitable for a wide range of cell types, including primary cells. Due to the combination of a minimal promoter and specific response elements, the system exhibits an excellent signal-to-noise ratio, making it more sensitive than traditional reporter gene detection methods. Furthermore, the luciferase reporter gene allows for non-invasive quantitative measurement via bioluminescence imaging, facilitating endpoint and longitudinal studies of Hh pathway regulation.
This reporter lentivirus has broad applications in basic research and drug development. Scientists use it to study Hh pathway activation under various physiological and pathological conditions, including cancer research, as aberrant Hh signaling is associated with many malignancies. The system is particularly valuable for screening small molecule modulators of the Hh pathway, serving as an important tool for developing Hh pathway inhibitors for cancer treatment. Researchers also utilize it to study the interactions between Hh signaling and other developmental pathways, and to characterize gene mutations affecting pathway components. The lentiviral vector format allows for the creation of stable reporter cell lines, which can be used for high-throughput screening of compound libraries.
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The clear, quantifiable luciferase readout allowed us to efficiently dissect the compound’s mechanism of action and downstream effects compared to controls.
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