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Cat. No. : CSC-RR01144
Host Cell : NIH3T3 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR01144 |
| Description | p53-Luc/EF1α-mCherry Reporter Cell Line - NIH3T3 |
| Product Type | Signaling pathway reporter cell line |
| Target Gene | p53-Luc/EF1α-mCherry |
| Host Cell | NIH3T3 |
| Host Cell Species | Mus musculus (Mouse) |
| 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 |
The p53-Luc/EF1α-mCherry Reporter Cell Line - NIH3T3 is a genetically engineered mouse fibroblast cell line developed from the widely used NIH3T3 background. It contains a p53-responsive luciferase reporter system, in which luciferase expression is controlled by p53 response elements, together with an EF1α-driven mCherry fluorescent marker. The p53-Luc reporter enables quantitative monitoring of p53 transcriptional activity through luminescence, while mCherry fluorescence provides a convenient indicator of reporter-cell identity, transduction efficiency, and cell distribution. As a stable reporter model, it is suitable for experiments requiring consistent and reproducible assessment of p53 pathway activation.
This reporter cell line is primarily used to study p53 signaling, a key pathway involved in DNA damage responses, cell-cycle regulation, senescence, and apoptosis. Treatment with genotoxic agents, oxidative stressors, radiation, or pathway-modulating compounds can induce p53 activity, resulting in increased luciferase expression that can be measured with a luminescence assay. The system is therefore useful for screening compounds that activate or inhibit p53-dependent transcription, evaluating the biological effects of anticancer agents, and investigating mechanisms associated with tumor suppressor regulation. The mCherry signal supports complementary fluorescence-based observation, allowing researchers to monitor cell morphology, localization, and relative cell abundance during experiments. In addition, the line can be applied to pathway validation, toxicity studies, drug-response profiling, and high-throughput screening.
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We used the p53-Luc/EF1α-mCherry NIH3T3 cell line for our DNA damage pathway research, and the results were outstanding. The mCherry signal provided a seamless way to normalize for cell viability and transfection efficiency. The p53-driven luciferase activity showed a high induction fold-change following treatment, making our data highly reproducible and statistically significant.
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