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-RR01042
Host Cell : J82 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR01042 |
| Description | J82-mScarlet/LUC cell line is engineered to co-express mScarlet and luciferase reporter genes in J82 cells. mScarlet and luciferase are useful biomarkers and are widely used in cell research to label and monitor various types of cells. This cell line is a powerful tool in both fluorescent and bioluminescent tracking of J82 cells. |
| Product Type | Stable cell line expressing mScarlet and luciferase reporter genes |
| Target Gene | mScarlet/LUC |
| Host Cell | J82 |
| Host Cell Species | Homo sapiens (Human) |
| Applications |
1) in vitro cell tracking by both the fluorescent and bioluminescent signal 2) monitor in vivo tumor growth using both the fluorescence and bioluminescence signal 3) anticancer drug development |
| Size | One vial of frozen cells, typically >1x10^6cells/vial |
| Stability | This cell line is stable at least 10 passages. |
| Quality Control |
1) fluorescence detection under microscopy 2) in vitro cell luciferase assay 3) mycoplasma detection |
| 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 |
| 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 |
J82 is a human urinary bladder carcinoma cell line established from a high-grade transitional cell carcinoma of the bladder. The cell line is characterized by aggressive growth behavior, high invasive capacity, and significant tumorigenic potential, making it a widely used model for studying advanced urothelial carcinoma. J82 cells harbor molecular alterations commonly associated with bladder cancer progression and have been extensively employed in investigations of oncogenic signaling, tumor invasion, metastasis, and therapeutic resistance. Owing to its aggressive phenotype, the cell line serves as a valuable platform for evaluating novel treatment strategies and elucidating mechanisms underlying bladder cancer development. The mScarlet/LUC Reporter Cell Line - J82 is generated through stable integration of the red fluorescent protein mScarlet and firefly luciferase (LUC) reporter genes into parental J82 cells. This dual-reporter system enables sensitive fluorescence imaging and quantitative bioluminescence monitoring while preserving the biological characteristics and tumorigenic properties of the original cell line.
The J82-mScarlet/LUC reporter cell line is widely utilized in bladder cancer research for dynamic assessment of tumor progression and therapeutic efficacy. Luciferase expression enables non-invasive, longitudinal monitoring of tumor burden, local invasion, and metastatic dissemination through bioluminescence imaging in xenograft models, allowing real-time evaluation of disease progression and treatment response. Meanwhile, mScarlet expression provides bright and stable red fluorescence for high-resolution visualization of cellular morphology, proliferation, migration, invasion, and tissue localization. This model is particularly valuable for screening anti-cancer compounds, evaluating targeted therapies, and investigating mechanisms of chemotherapy resistance in advanced urothelial carcinoma. In addition, the dual-reporter platform supports studies of epithelial–mesenchymal transition, tumor–microenvironment interactions, cancer stem cell-associated properties, and signaling pathways involved in bladder cancer aggressiveness and metastasis. With stable reporter expression and robust imaging performance, the J82-mScarlet/LUC cell line serves as a reliable and reproducible tool for preclinical drug development and translational research in bladder cancer.
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Establishing orthotopic bladder cancer models is traditionally challenging, but these J82 reporter cells made non-invasive tracking incredibly straightforward. The dual reporters are uniformly expressed across the population, and cell viability upon thawing was over 90%. Highly recommended.
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