Transfected Stable Cell Lines
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Cat. No. : CSC-RR01140
Host Cell : NIH3T3 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR01140 |
| Description | AP1-Luc/EF1α-mCherry Reporter Cell Line - NIH3T3 |
| Product Type | Signaling pathway reporter cell line |
| Target Gene | AP1-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 |
The AP1-Luc/EF1α-mCherry reporter cell line (based on NIH3T3) is a genetically engineered mouse embryonic fibroblast reporter line. It incorporates a firefly luciferase expression system driven by AP-1 response elements, allowing for the monitoring of AP-1 signaling pathway activation through the detection of bioluminescence. Additionally, the cell line constitutively expresses the fluorescent protein mCherry under the control of the EF1α promoter, providing a stable fluorescent marker for cell identification and tracking. AP-1 (Activator Protein 1) is a transcription factor complex—composed primarily of Jun, Fos, ATF, and related proteins—that plays a critical role in cellular responses to growth factors, cytokines, stress, inflammation, differentiation, and oncogenic stimuli. This dual-reporter system combines a pathway-specific luciferase signal with a constitutive red fluorescent signal, facilitating cell visualization, assessment of culture quality, and the normalization of experimental data.
This reporter cell line is primarily used for in vitro studies of the activation and regulatory mechanisms of the AP-1 pathway. It can be applied to screen for small-molecule compounds, biological agents, natural products, and various genetic interventions that activate or inhibit AP-1-related signaling pathways. Researchers can stimulate the cells—using mitogens, inflammatory mediators, oxidative stressors, or other test substances—and subsequently quantify luciferase activity as an indicator of transcriptional pathway activation. The EF1α-mCherry signal can be used to monitor cell distribution, estimate cell numbers, and detect any changes in cell morphology or viability during experiments. The cell line is suitable for high-throughput screening, mechanism-of-action studies, pathway profiling, toxicity assessment, and the validation of upstream targets within stress-response networks and signaling crosstalk involving MAPK, JNK, p38, and NF-κB.
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We are very satisfied with the AP1-Luc/EF1α-mCherry Reporter Cell Line - NIH3T3. It has been vital for our research into MAPK signaling and cell transformation. The reporter activity is highly specific, and the dual-color system makes data interpretation straightforward. It’s a very cost-effective and reliable solution for monitoring AP-1 transcriptional activity.
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