Transfected Stable Cell Lines
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Cat. No. : CSC-RR00725
Host Cell : SGC7901 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR00725 |
| Description | SGC7901-Luc reporter cell line is engineered to stably express Luciferase reporter gene in human gastric adenocarcinoma cell line SGC7901. |
| Product Type | Stable cell line constitutively expressing luciferase reporter gene |
| Target Gene | Luc |
| Host Cell | SGC7901 |
| Host Cell Species | Homo sapiens (Human) |
| Reporter | Luciferase reporter gene |
| Applications |
1) in vitro cell tracking by bioluminescent signal 2) monitor in vivo tumor growth using the 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) Luciferase activity assay 2) 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 |
SGC-7901 cells are a human gastric adenocarcinoma–derived cell line widely used as an in vitro model for studying gastric cancer biology and tumor progression of the digestive system. These cells are characterized by epithelial-like morphology, high proliferative capacity, and genetic alterations commonly associated with poorly differentiated gastric carcinoma. SGC-7901 cells exhibit dysregulated signaling pathways involved in cell proliferation, apoptosis resistance, invasion, and epithelial–mesenchymal transition (EMT), making them suitable for investigating mechanisms underlying gastric tumor growth and metastasis. The Luciferase Reporter Cell Line – SGC-7901 is generated by stable integration of a luciferase reporter construct driven by pathway-responsive elements or transcription factor–specific promoters into the parental SGC-7901 background, enabling real-time and quantitative monitoring of transcriptional and signaling activities while preserving the intrinsic biological properties of the original gastric cancer cell line.
The Luciferase Reporter Cell Line – SGC-7901 is widely applied in gastric cancer research, oncogenic signaling studies, and anti-tumor drug screening. It is particularly useful for evaluating key pathways implicated in gastric carcinoma progression, including PI3K/AKT/mTOR, MAPK/ERK, NF-κB, Wnt/β-catenin, and TGF-β/SMAD signaling, which are closely associated with tumor growth, metastasis, and therapy resistance. The luciferase reporter system provides a sensitive and reliable quantitative readout for assessing pathway activation or inhibition in response to pharmacological compounds, biologics, or genetic modulation. This model is commonly used in high-throughput screening of anti-gastric cancer agents, as well as in mechanistic studies of tumor invasion, angiogenesis, and apoptotic regulation. Its stability, reproducibility, and strong signal sensitivity make it a valuable platform for both basic research and preclinical evaluation of targeted therapies for gastric cancer.
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We use the SGC7901 luciferase reporter line routinely for wound-healing migration assays and compound toxicity screening. The cells maintain their adherent, epithelial morphology, and the luciferase signal is linear across a wide cell density range. After six months of continuous use, we have not observed any signal attenuation.
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