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NFκB-Luc/EF1α-mCherry Reporter Cell Line - HepG2

For research use only. Not intended for any clinical use.

Cat. No. :   CSC-RR01068

Host Cell :   HepG2 Size :   >1x106 frozen cells/vial

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Cat. No. CSC-RR01068
Description NFκB-Luc/EF1α-mCherry Reporter Cell Line - HepG2
Product Type Signaling pathway reporter cell line
Target Gene NFκB-Luc/EF1α-mCherry
Host Cell HepG2
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
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The HepG2 cell line, derived from human hepatocellular carcinoma tissue, remains one of the most reliable models for studying human liver function, drug metabolism, and toxicology due to its retention of hepatocyte-like characteristics. The NFkB-Luc/EF1α-mCherry Reporter Cell Line - HepG2 is a genetically engineered version of this model designed for the sensitive detection of NF-kappa B (NF-κB) pathway activity. This specific line features a dual-reporter system: the firefly luciferase gene is controlled by a synthetic promoter containing multiple NF-κB response elements, while the mCherry fluorescent protein is constitutively expressed under the EF1α promoter. This configuration allows for the quantitative measurement of transcriptional activation through bioluminescence, alongside a stable red fluorescent signal that serves as an internal control for cell density, viability, and normalization across different experimental conditions.

This reporter system is particularly effective for high-throughput screening of anti-inflammatory drugs and the assessment of liver-specific inflammatory responses. By monitoring luciferase expression, researchers can accurately gauge the activation of the NF-κB pathway in response to external stimuli like TNF-alpha or interleukin-1 beta, which are critical in the study of chronic liver diseases and immune regulation. The integration of mCherry provides a distinct advantage by allowing for real-time monitoring of cell health, ensuring that any observed reduction in luciferase activity is a result of pathway inhibition rather than non-specific drug-induced cell death. Consequently, this cell line is a powerful tool for investigating the molecular mechanisms of liver inflammation, exploring the effects of various cytokines, and developing therapeutic interventions for conditions such as hepatitis and non-alcoholic fatty liver disease. The stability and reproducibility of the reporter signals make it ideal for long-term assays and complex drug toxicity evaluations in the pharmaceutical industry.

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Customer Reviews
Highly recommended for anyone studying hepatic inflammation.

NFκB is a tricky pathway due to potential high background, but this Creative Biogene cell line performs beautifully. We used it for inflammation modeling in HepG2 cells. The dual-reporter design is a lifesaver for eliminating false positives caused by cytotoxicity. Highly recommended for anyone studying hepatic inflammation.

United States

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