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Cat. No. : CSC-RR01158
Host Cell : HEK293 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR01158 |
| Description | ARE-Luc/EF1α-mCherry Reporter Cell Line - HEK293 |
| Product Type | Signaling pathway reporter cell line |
| Target Gene | ARE-Luc/EF1α-mCherry |
| Host Cell | HEK293 |
| Host Cell Species | Homo sapiens (Human) |
| Applications | Signaling pathway studies and screening assay |
| Size | One vial of frozen cells, typically >1x10^6cells/vial |
| Stability | This cell line is stable at least 10 passages. |
| Storage | Liquid nitrogen |
| Shipping | Dry ice |
| Revival | Rapidly thaw cells in a 37°C water bath. Transfer contents into a tube containing pre-warmed media. Centrifuge cells and seed into a 25 cm2 flask containing pre-warmed media. |
| Growth Properties | Adherent cell line |
| Mycoplasma | Negative |
| Format | One frozen vial containing millions of cells |
| Storage | Liquid nitrogen |
| Safety Considerations |
The following safety precautions should be observed. 1. Use pipette aids to prevent ingestion and keep aerosols down to a minimum. 2. No eating, drinking or smoking while handling the stable line. 3. Wash hands after handling the stable line and before leaving the lab. 4. Decontaminate work surface with disinfectant or 70% ethanol before and after working with stable cells. 5. All waste should be considered hazardous. 6. Dispose of all liquid waste after each experiment and treat with bleach. |
| Ship | Dry ice |
ARE-Luc/EF1α-mCherry Reporter Cell Line – HEK293 is a genetically engineered human embryonic kidney 293 cell line designed for sensitive monitoring of antioxidant response element (ARE)-dependent transcriptional activity. The reporter construct contains luciferase driven by an ARE-responsive promoter, enabling quantitative detection of signaling mediated primarily by the Nrf2/Keap1 pathway. In parallel, mCherry fluorescent protein is constitutively expressed under the human EF1α promoter, providing a stable visual marker for cell identification, culture monitoring, and normalization of cell number or transduction efficiency. HEK293 cells offer robust growth characteristics, high transfectability, and reliable assay performance, making this dual-reporter cell line a convenient tool for oxidative stress research. Upon activation of ARE-regulated transcription, luciferase expression increases and can be measured using standard luminescence-based assays, while the red fluorescent signal supports rapid observation by fluorescence microscopy or flow cytometry.
This reporter cell line is well-suited for screening compounds that activate or inhibit the Nrf2/ARE signaling pathway, including antioxidants, electrophilic compounds, environmental chemicals, natural products, and drug candidates. It can be used to assess cellular responses to oxidative stress, investigate the mechanisms of action of redox-active molecules, and characterize regulators of cytoprotective gene expression. The constitutive expression of EF1α-mCherry is particularly useful for high-content imaging, the optimization of cell-based assays, and experiments requiring the verification of cell viability, morphology, or culture consistency. In drug discovery, this cell line can be employed for the initial screening and subsequent validation of potential Nrf2 modulators. Furthermore, it has applications in toxicology, where it can be used to evaluate the risk of a test substance inducing oxidative stress. By combining bioluminescence and fluorescence detection, this system provides a practical and versatile platform for pathway analysis, compound characterization, and the development of assays targeting antioxidant defense mechanisms.
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We utilized this ARE reporter cell line to screen for antioxidant compounds. The Nrf2-mediated luciferase induction was clear and dose-dependent. Having the constitutive mCherry expression helped us distinguish between true pathway inhibition and potential cytotoxicity of our compounds.
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