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-RR01113
Host Cell : T24 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR01113 |
| Description | ISRE-Luc/EF1α-mCherry Reporter Cell Line - T24 |
| Product Type | Signaling pathway reporter cell line |
| Target Gene | ISRE-Luc/EF1α-mCherry |
| Host Cell | T24 |
| 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 - T24 is a stable human bladder carcinoma cell line designed to quantitatively monitor the activation of the JAK-STAT signaling pathway. This dual-reporter system incorporates the Firefly luciferase gene under the transcriptional control of a promoter containing multiple Interferon-Stimulated Response Elements (ISRE). When Type I or Type III interferons bind to their respective receptors, they trigger a signaling cascade that results in the binding of transcription factors to the ISRE, subsequently driving luciferase expression in a concentration-dependent manner. For improved reliability, the cell line constitutively expresses mCherry fluorescent protein under the elongation factor 1-alpha (EF1α) promoter. This internal marker facilitates the normalization of luciferase signals against cell density and serves as a tool for visual verification and selection during experimental procedures.
In the context of biomedical research and drug development, this reporter cell line offers a streamlined platform for investigating innate immune responses and screening therapeutic candidates. It is extensively used in high-throughput assays to evaluate the potency of interferon-based drugs and to identify small molecules that modulate the JAK-STAT pathway, which is central to antiviral defense and tumor immunology. Beyond drug screening, the T24 reporter line is effective for studying viral interference with host signaling and for assessing the bioactivity of cytokines in complex biological matrices. Its stable expression profile and robust bioluminescent output make it an essential tool for characterizing the efficacy of anti-inflammatory compounds and validating the molecular targets of novel immunotherapies within an epithelial cell background.
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The ISRE element activation provides clear readouts of interferon stimulation, while the mCherry reporter eliminates the need for additional fluorescent staining. Perfect for high-content screening platforms.
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