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Cat. No. : CSC-RR01161
Host Cell : HEK293 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR01161 |
| Description | NFκB-Luc/EF1α-mCherry Reporter Cell Line - HEK293 |
| Product Type | Signaling pathway reporter cell line |
| Target Gene | NFκB-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 |
NFκB-Luc/EF1α-mCherry Reporter Cell Line - HEK293 is a genetically engineered human embryonic kidney 293 cell line designed for sensitive monitoring of nuclear factor kappa B (NF-κB) pathway activity. The cells stably express a firefly luciferase reporter driven by NF-κB-responsive elements, allowing pathway activation to be quantified through luminescence measurement. In parallel, mCherry is constitutively expressed under the human elongation factor 1 alpha (EF1α) promoter, providing a robust fluorescent marker for cell identification, normalization, and assessment of transfection or treatment-related effects on cell number. NF-κB is a central transcription factor involved in inflammatory signaling, innate and adaptive immune responses, cellular stress, proliferation, and survival. In resting cells, NF-κB is retained in the cytoplasm by inhibitory IκB proteins. Stimulation by cytokines, pathogen-associated molecules, oxidative stress, or other activators promotes IκB degradation and NF-κB nuclear translocation, resulting in transcriptional activation of NF-κB target genes and luciferase expression in this reporter system.
This reporter cell line is designed for the cellular screening and mechanistic study of modulators of the NF-κB signaling pathway. It can be used to evaluate a wide range of substances that regulate NF-κB pathway activity, including anti-inflammatory compounds, immune agonists, kinase inhibitors, biologics, natural products, and therapeutic drug candidates. Typical applications include assessing cellular responses to TNF-α, IL-1β, lipopolysaccharide (LPS), Toll-like receptor (TLR) agonists, and other inflammatory stimuli, as well as determining dose-response relationships, potency, efficacy, and pathway selectivity. The luciferase-based detection method enables rapid, quantitative, and scalable assays in a multi-well plate format, making it well-suited for high-throughput or medium-throughput drug discovery workflows. Furthermore, this cell line can be utilized in research areas such as inflammation, cancer biology, infection, stress responses, and signal transduction—fields in which NF-κB activity is frequently employed as a key functional endpoint.
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We have integrated this NFκB reporter into our primary HTS workflow. The cells grow vigorously and the reporter induction remains stable over long-term culture. The dual-color system is brilliant for ensuring our hits are not just artifacts of cell death.
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