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Cat. No. : CSC-RR01132
Host Cell : U87MG Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR01132 |
| Description | NFκB-Luc/EF1α-mCherry Reporter Cell Line - U87MG |
| Product Type | Signaling pathway reporter cell line |
| Target Gene | NFκB-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 |
NFκB-Luc/EF1α-mCherry Reporter Cell Line - U87MG is a genetically engineered human glioblastoma cell line derived from the parental U87MG model. The cells contain a luciferase reporter gene controlled by an NFκB-responsive promoter, allowing activation of the NFκB signaling pathway to be quantified through luminescence. They also stably express mCherry under the EF1α promoter, providing a constitutive red fluorescent signal for visual identification, cell tracking, and normalization of cell number or viability. This dual-reporter design combines pathway-specific bioluminescence with stable fluorescence, making the cell line suitable for reproducible, real-time analysis of NFκB activity in a glioblastoma-relevant cellular background.
The reporter cell line is primarily used to evaluate compounds, biologics, genetic interventions, and cellular stimuli that regulate NFκB signaling. It can support high-throughput screening for NFκB inhibitors or activators, mechanism-of-action studies, and investigations of inflammatory, immune, stress, and survival pathways in glioblastoma cells. The luciferase readout provides a sensitive, quantitative measure of transcriptional activity, while mCherry fluorescence enables routine culture monitoring, imaging, cell counting, and quality control. Researchers may apply the model to assess responses to cytokines such as TNF-α or IL-1β, examine pathway modulation induced by pharmacological treatments, and compare gene knockdown or overexpression conditions. It is also useful for studying tumor–immune interactions, screening anti-inflammatory or anticancer candidates, and establishing co-culture or drug-response assays.
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This is an excellent reporter cell line for studying the inflammatory microenvironment of glioblastoma. The NFκB-Luc response is rapid and highly sensitive to TNFα stimulation. The inclusion of the mCherry reporter ensures that we can distinguish between pathway inhibition and general cytotoxicity, which is critical for our drug discovery efforts.
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