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. : LVG00094Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00094Z |
| Description | Lentivirus particles containing luciferase reporter gene under the control of a minimal promoter and Glucocorticoid response element (GRE/GR). |
| 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 GR luciferase reporter lentiviral vector is designed to provide a highly sensitive reporting system for studying the glucocorticoid receptor (GR) signaling pathway. These lentiviral particles contain a firefly or Renilla luciferase reporter gene, which is regulated by a minimal promoter and multiple glucocorticoid response elements (GREs). This lentiviral vector system offers several key advantages: stable genomic integration allowing for long-term studies in both dividing and non-dividing cells; high transduction efficiency in a variety of cell types; and stable reporter gene expression even after multiple passages. The GRE-driven design ensures a specific response to glucocorticoid stimulation, while the minimal promoter minimizes basal activity. Compared to transient transfection methods, this system demonstrates significantly higher sensitivity and allows for quantitative measurement of GR activation via luminescence detection.
This reporter lentivirus has broad applications in pharmacological research and molecular biology. It is an excellent tool for screening GR agonists/antagonists, evaluating steroid receptor interactions, and studying glucocorticoid signaling mechanisms. Researchers utilize this system to study GR-mediated gene regulation in various cell models, including primary cells and difficult-to-transfect cell lines. The stable integration characteristic enables the creation of reporter cell lines for long-term drug development projects and high-throughput screening applications. Furthermore, this technology facilitates the study of GR-related diseases, such as inflammation, autoimmune diseases, and metabolic syndrome, by precisely quantifying pathway activation.
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Comparing different GR agonists required a highly sensitive reporter. This lentivirus-based system outperformed our transient transfection experiments significantly. The signal-to-noise ratio was excellent, allowing us to detect subtle differences in potency and efficacy between compounds with great confidence.
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