Transfected Stable Cell Lines
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Cat. No. : CSC-RR01190
Host Cell : ECA-109 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR01190 |
| Description | This cell line is engineered to stably exprress GFP and luciferase (GFP/Luc) reporter genes in ECA109 cells. It is a useful tool for both fluorescent and bioluminescent tracking of ECA109 cells. |
| Product Type | Bioluminescent Reporter Cell Lines/Fluorescent Reporter Cell Lines |
| Target Gene | GFP/Luc |
| Host Cell | ECA-109 |
| Host Cell Species | Homo sapiens (Human) |
| Applications | in vitro cell tracking and in vivo cell imaging |
| 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 |
ECA109 is an adherent human cancer cell line associated with esophageal squamous cell carcinoma and has been used extensively in experimental studies of esophageal tumor biology. The cells display epithelial growth characteristics and can form tumors in immunodeficient mice under appropriate experimental conditions. GFP/Luc Reporter Cell Line - ECA109 is an engineered derivative expressing green fluorescent protein and firefly luciferase. GFP enables direct visualization of reporter-positive cells by fluorescence microscopy or flow cytometry, while luciferase produces bioluminescence after exposure to a compatible luciferin substrate. These complementary signals allow researchers to identify the cells visually and obtain a sensitive quantitative measurement from the same model.
The dual-reporter line is suitable for studying esophageal cancer cell proliferation, survival, migration, invasion, and treatment response. GFP fluorescence can be used to examine cell morphology, localization, and interactions with stromal or immune cells in two-dimensional cultures, spheroids, and other co-culture systems. Luciferase provides a convenient readout for viability and cytotoxicity assays, supporting compound screening and comparisons of chemotherapy, targeted agents, biologics, or combination treatments. In xenograft studies, bioluminescence imaging may allow repeated, non-invasive monitoring of tumor establishment, growth, dissemination, and therapeutic response in the same animal. GFP can complement these measurements by supporting ex vivo imaging and identification of reporter-positive cells in excised tissues. Together, the two reporters make this line useful for mechanistic studies, drug-response evaluation, and preclinical imaging research involving esophageal squamous cell carcinoma.
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The ECA109 GFP/Luc line has been great for tracking cells by microscopy and for quantitative readouts in drug screens. Quick to recover after thawing and consistent across passages.
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