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Cat. No. : CSC-RR01129
Host Cell : U87MG Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR01129 |
| Description | ARE-Luc/EF1α-mCherry Reporter Cell Line - U87MG |
| Product Type | Signaling pathway reporter cell line |
| Target Gene | ARE-Luc/EF1α-mCherry |
| Host Cell | U87MG |
| 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 - U87MG is a genetically engineered human glioblastoma cell line derived from U87MG cells. It contains an antioxidant response element (ARE)-driven luciferase reporter system for monitoring the transcriptional activity of the Nrf2/ARE signaling pathway, together with an EF1α promoter-driven mCherry fluorescent marker for stable cell identification and experimental tracking. The luciferase signal reflects changes in ARE-dependent gene expression and can be quantified using a luminescence-based assay, while mCherry fluorescence provides a convenient visual indicator of cell presence, morphology, and transduction stability. This dual-reporter design combines sensitive pathway analysis with straightforward fluorescence monitoring in a well-established glioblastoma cellular background.
This reporter cell line is primarily intended for research on the Nrf2/ARE pathway, oxidative stress, antioxidant responses, and cytoprotective mechanisms in glioblastoma cells. It can be used to evaluate compounds that activate or inhibit ARE-mediated transcription, screen potential antioxidants and electrophilic agents, and investigate the molecular effects of environmental stressors, pharmaceutical candidates, and natural products. The system is also useful for studying drug-induced oxidative responses, cellular defense mechanisms, and signaling interactions associated with tumor biology. In high-throughput screening, luciferase measurements enable rapid and quantitative comparison of pathway activity across multiple treatment conditions, whereas mCherry fluorescence supports cell number estimation, assay quality control, and visualization of cellular distribution. Researchers may further apply this model to mechanism-of-action studies, preliminary toxicity evaluation, combination treatment assessment, and validation of Nrf2-related targets.
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For our research into Nrf2/ARE signaling, this reporter cell line has been invaluable. The U87MG cells maintain their expected morphology and growth characteristics while providing a sensitive readout of oxidative stress levels. The integration of mCherry under the EF1α promoter is a brilliant touch for normalizing results across different treatment concentrations.
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