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Cat. No. : CSC-RR01133
Host Cell : U87MG Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR01133 |
| Description | p53-Luc/EF1α-mCherry Reporter Cell Line - U87MG |
| Product Type | Signaling pathway reporter cell line |
| Target Gene | p53-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 |
The p53-Luc/EF1α-mCherry reporter cell line (based on U87MG) is a genetically engineered human glioblastoma model derived from the U87MG cell line. It incorporates a firefly luciferase reporter gene driven by a p53-responsive promoter, enabling the quantitative monitoring of transcriptional activity regulated by the p53 signaling pathway. Additionally, the mCherry fluorescent protein is constitutively expressed under the control of the EF1α promoter, providing a stable fluorescent marker for the identification and tracking of these reporter cells. This dual-reporter system combines an inducible luminescent signal with a continuous red fluorescent signal, allowing researchers to assess p53 pathway activation while simultaneously observing cell distribution, morphology, and viability.
The p53-Luc/EF1α-mCherry reporter cell line (based on U87MG) is well-suited for investigating p53-mediated responses within the context of glioblastoma biology and anticancer drug development. It can be utilized to screen for small-molecule compounds, biologics, and combination therapies that activate or inhibit p53-dependent transcription. The luciferase signal intensity serves as a sensitive and quantifiable readout for dose-response studies, high-throughput screening, and the analysis of pathway regulation during mechanism-of-action studies. The constitutively expressed mCherry signal facilitates the normalization of experimental data and supports applications such as live-cell imaging, cell counting, transduction monitoring, and quality control. Furthermore, this model can be applied to research concerning DNA damage, cellular stress, apoptosis, therapeutic resistance, and gene regulation. By integrating a pathway-specific reporter system with a stable fluorescent reference, this cell line enhances experimental consistency and provides a practical platform for translational research focused on the p53 signaling pathway in glioblastoma.
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The cells are easy to culture and provide a very reliable luciferase readout. Creative Biogene’s technical support was also very helpful in providing detailed protocols.
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