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TNFαPro-Luc/EF1α-mCherry Reporter Cell Line - NIH3T3

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

Cat. No. :   CSC-RR01139

Host Cell :   NIH3T3 Size :   >1x106 frozen cells/vial

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Cell Line Information

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Cat. No. CSC-RR01139
Description TNFαPro-Luc/EF1α-mCherry Reporter Cell Line - NIH3T3
Product Type Signaling pathway reporter cell line
Target Gene TNFαPro-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
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TNFαPro-Luc/EF1α-mCherry Reporter Cell Line - NIH3T3 is a genetically engineered mouse embryonic fibroblast cell line derived from NIH3T3 cells. It contains a luciferase reporter gene controlled by the promoter region of tumor necrosis factor alpha (TNFα), allowing TNFα promoter activity to be monitored through a quantifiable luminescent signal. The cell line also constitutively expresses mCherry under the control of the EF1α promoter, providing a stable fluorescent marker for identifying and tracking the cells. With the biological characteristics of NIH3T3 fibroblasts and dual luciferase–fluorescence readouts, this reporter system offers a convenient and sensitive platform for studying inflammatory signaling and transcriptional regulation. Luciferase activity generally reflects changes in TNFα promoter activation, while mCherry fluorescence can be used for cell localization, transfection assessment, and normalization of cell numbers.

This reporter cell line is suitable for investigating the molecular mechanisms that regulate TNFα expression in inflammatory and immune-related pathways. It can be used to evaluate the effects of cytokines, pathogen-associated stimuli, small-molecule compounds, biologics, and gene-editing approaches on TNFα transcriptional activity. The system is particularly useful for screening anti-inflammatory drugs and identifying compounds that either suppress or enhance TNFα-related signaling. Researchers may also apply it to study the activation of pathways such as NF-κB, MAPK, and other transcriptional networks involved in inflammatory responses. In addition, the line supports high-throughput screening, promoter activity analysis, pathway validation, and comparative assessment of treatment conditions. The mCherry signal provides an independent visual reference, helping distinguish changes in reporter activity from variations caused by cell density, viability, or experimental handling.

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Customer Reviews
Ideal for High-Throughput Anti-inflammatory Screening

This TNFα promoter reporter line has been instrumental in our drug discovery pipeline. The sensitivity to TNFα pathway modulators is excellent. We particularly appreciate the stability of the EF1α-mCherry marker, which allows for real-time monitoring of cell health during long-term assays. The quality of the cell line exceeded our expectations.

United States

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