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. : LVG00095Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00095Z |
| Description | Lentivirus particles containing luciferase reporter gene under the control of a minimal promoter and Heat Shock response element (HSE/HSF1). |
| 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 HSF1 luciferase reporter gene lentiviral vector is a powerful research tool specifically designed for studying the heat shock response pathway and the activity of HSF1 (Heat Shock Factor 1). This lentiviral vector contains a luciferase reporter gene regulated by a minimal promoter and a heat shock response element (HSE/HSF1). The lentiviral delivery system offers several key advantages: it efficiently and stably transduces both dividing and non-dividing cells, enables long-term gene expression through genomic integration, and allows for the selection of stable cell lines. This reporter construct is specifically designed to respond to HSF1 activation, making it highly sensitive to heat shock and other cellular stresses that trigger the heat shock response pathway.
This reporter gene lentivirus has broad applications in biomedical research and drug discovery. Scientists primarily use it to study cellular stress responses, particularly the activation and regulation of the HSF1-mediated pathway under various stress conditions (e.g., heat shock, oxidative stress, or chemical stress). This system is crucial for screening and characterizing compounds that modulate HSF1 activity, including potential therapeutic drugs targeting protein homeostasis pathways. Researchers can utilize this tool to investigate the induction mechanisms of heat shock proteins (HSPs), protein folding diseases, and cellular responses to environmental stressors. The luciferase reporter gene provides quantitative measurements through luminescence detection, enabling high-throughput screening applications. Furthermore, the lentiviral delivery system allows for the creation of stable reporter gene cell lines, which can be used for long-term studies of HSF1 dynamics or for monitoring stress responses over time in various experimental models, including primary cells that are difficult to transfect using traditional methods.
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