Transfected Stable Cell Lines
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Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : CSC-RR01095
Host Cell : PANC-1 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR01095 |
| Description | ISRE-Luc/EF1α-mCherry Reporter Cell Line - PANC-1 |
| Product Type | Signaling pathway reporter cell line |
| Target Gene | ISRE-Luc/EF1α-mCherry |
| Host Cell | PANC-1 |
| 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 |
The ISRE-Luc/EF1α-mCherry Reporter Cell Line - PANC-1 is a dual-reporter human pancreatic carcinoma cell line specifically developed for monitoring the Interferon-Stimulated Response Element (ISRE) signaling pathway. It stably integrates the firefly luciferase gene driven by a promoter containing multiple tandem ISRE repeats, enabling quantitative and sensitive measurement of type I and type III interferon-induced transcriptional activation. Concurrently, the cell line constitutively expresses mCherry red fluorescent protein under the control of the strong EF1α promoter, serving as an internal control for cell viability, signal normalization, and direct visual monitoring. Established from the human PANC-1 line, this model delivers high signal-to-noise performance for studying innate immune signaling in pancreatic cancer cells.
This specialized cell line is ideal for high-throughput screening of immunomodulatory compounds, small molecules, and biological agents that activate or inhibit the JAK-STAT/ISRE signaling cascade. Researchers utilize it to measure cell-based interferon activity, assess host antiviral signaling responses, and analyze tumor cell reactivity to cytokine therapies. By normalizing inducible firefly luciferase luminescence against baseline mCherry fluorescence, accurate evaluation of pathway activity is maintained while controlling for cell density variation or compound toxicity. Furthermore, the constitutive mCherry reporter facilitates real-time cell tracking, live-cell imaging, and flow cytometry assays, making it a valuable tool for oncology, immunology, and targeted drug discovery workflows.
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We utilized this ISRE-Luc PANC-1 line to study Type I interferon signaling pathways. The cell line is very responsive to IFN treatment, providing a high dynamic range for our luciferase assays. The co-expressed mCherry marker is extremely helpful for visualizing the cells before running the lysis steps.
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