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-RR01114
Host Cell : T24 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR01114 |
| Description | Myc-Luc/EF1α-mCherry Reporter Cell Line - T24 |
| Product Type | Signaling pathway reporter cell line |
| Target Gene | Myc-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 Myc-Luc/EF1α-mCherry reporter cell line (based on T24 cells) is a dual-labeled, engineered cellular tool derived from the human bladder transitional cell carcinoma T24 cell line. This model is specifically designed to quantitatively monitor the transcriptional activity of the c-Myc oncogene—a central regulator of cell cycle progression, metabolism, and apoptosis. The genetic architecture of this cell line incorporates a synthetic promoter consisting of multiple tandem c-Myc response elements (MREs) positioned upstream of a firefly luciferase gene. To enhance its utility, the cell line also constitutively expresses the fluorescent protein mCherry under the control of an EF1α promoter. This design provides a reliable internal reference, allowing for the normalization of luciferase signals against cell number, and facilitates long-term live-cell imaging. As these genetic cassettes are stably integrated into the genome, the cell line maintains consistent reporter performance over multiple passages, making it a robust platform for oncology research.
In terms of application, this reporter cell line is primarily used for high-throughput screening (HTS) to identify and validate inhibitors of the Myc signaling pathway. Given that Myc dysregulation is a hallmark of many aggressive cancers, this T24-based reporter line enables sensitive monitoring of drug-induced changes in Myc-mediated transcription via straightforward bioluminescence assays. Beyond drug discovery, it serves as an ideal system for functional genomics studies—such as those involving CRISPR-based gene knockout or RNA interference—aiding in the dissection of the complex regulatory networks that control Myc expression. Furthermore, the inclusion of the red fluorescent marker mCherry allows the cell line to be used in co-culture experiments or as a tracer in xenograft models, enabling the monitoring of tumor growth and reporter activity within a physiological context. By providing both quantitative readouts and visual tracking capabilities, this cell line streamlines the assessment of therapeutic efficacy and the underlying mechanisms of signal transduction.
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We utilized this T24 reporter line to screen small molecules targeting Myc-driven proliferation in bladder cancer. The assay window is wide, and the cells recover well after thawing. It is a high-quality product that streamlined our drug discovery pipeline.
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