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. : LVG00090Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00090Z |
| Description | Lentivirus particles containing luciferase reporter gene under the control of a minimal promoter and ER stress Activating Transcription Factor 6 (ATF6) 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 ATF6 luciferase reporter lentiviral vector is a genetically engineered viral vector system designed for sensitive and quantitative monitoring of endoplasmic reticulum (ER) stress via the ATF6 signaling pathway. This lentiviral vector contains a firefly luciferase reporter gene driven by a minimal promoter, which is serially linked to multiple ATF6 response elements (ER stress response elements). The lentiviral delivery system offers several significant advantages: high transduction efficiency in both dividing and non-dividing cells, stable genomic integration for long-term studies, and consistent reporter gene expression across cell populations. Compared to transient transfection methods, this lentiviral approach provides more reliable and reproducible results while minimizing experimental variability.
This ATF6 reporter lentivirus has broad applications in ER stress research and drug discovery. Scientists primarily utilize it to study the unfolded protein response (UPR) pathway mediated by ATF6 activation under ER stress conditions. The luciferase reporter gene allows for quantitative measurement of ATF6 transcriptional activity through simple luminescence detection, facilitating high-throughput screening of compounds that modulate ER stress. Researchers can apply this tool to study ATF6 activation in various disease models, including neurodegenerative diseases, diabetes, cancer, and inflammatory diseases where ER stress plays a pathological role. The system is particularly valuable for identifying novel ER stress modulators, characterizing ATF6 pathway inhibitors/activators, and understanding cellular responses to pharmacological ER stressors such as tunicamycin or thapsigargin. Furthermore, the lentiviral vector format makes it suitable for generating stable reporter cell lines for long-term mechanistic studies or repeated drug screening.
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We were impressed by the high sensitivity of the ATF6 Luciferase Reporter Lentivirus. It allowed us to detect even minimal changes in ATF6 activation levels, which was crucial for our cellular stress response investigations.
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