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CBF/NF-Y/YY1 Luciferase Reporter Lentivirus

For research use only. Not intended for any clinical use.

Cat. No. :   LVG00091Z

Storage :   -80℃ Shipping :   Frozen on dry ice

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Cat. No. LVG00091Z
Description Lentivirus particles containing luciferase reporter gene under the control of a minimal promoter and ER Stress CBF/NF-Y/YY1 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.
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The CBF/NF-Y/YY1 luciferase reporter lentiviral vector is a powerful tool for studying the transcriptional regulation of genes controlled by CBF/NF-Y/YY1 response elements. This lentiviral vector contains a luciferase reporter gene driven by a minimal promoter and an ER stress-responsive CBF/NF-Y/YY1 response element, enabling sensitive quantitative detection of transcriptional activity. The lentiviral delivery system offers several advantages, including high transduction efficiency in both dividing and non-dividing cells, stable integration into the host genome for long-term expression, and the ability to infect a wide range of cell types. Furthermore, the use of a minimal promoter reduces background noise, ensuring a high signal-to-noise ratio for accurate measurements.

This reporter system is particularly suitable for studying the molecular mechanisms of ER stress responses mediated by CBF/NF-Y/YY1 transcription factors. Researchers can use it to screen for compounds or conditions that modulate the activity of these transcription factors, investigate the effects of gene perturbations on their regulatory pathways, or monitor dynamic changes in transcriptional activity in real-time. The luciferase reporter gene provides quantitative readouts, enabling high-throughput screening and dose-response analysis. Additionally, the stable integration feature allows for the creation of cell lines with stable reporter gene expression, facilitating long-term studies and reducing experimental variability. This system is widely applicable in fields such as cancer research, immunology, and neurodegenerative diseases, where ER stress and its regulatory pathways play a crucial role.

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Customer Reviews
Exceptional Consistency

The consistency of our results improved remarkably after incorporating this lentiviral reporter. Each experiment provided clear, quantifiable data, enabling us to confidently interpret CBF/NF-Y/YY1-mediated cellular pathways.

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