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-RR01078
Host Cell : SGC7901 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR01078 |
| Description | NFκB-Luc/EF1α-mCherry Reporter Cell Line - SGC-7901 |
| Product Type | Signaling pathway reporter cell line |
| Target Gene | NFκB-Luc/EF1α-mCherry |
| Host Cell | SGC7901 |
| 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 |
SGC-7901 is a human gastric adenocarcinoma cell line originally isolated from a metastatic lymph node of a female patient with advanced stomach cancer. It grows as an adherent epithelial monolayer and is widely used as a representative gastric cancer model for studying tumor proliferation, drug response, and inflammation-linked signaling. The NFκB-Luc/EF1α-mCherry Reporter Cell Line - SGC-7901 is built on this background by stably integrating a firefly luciferase reporter driven by multiple NFκB response elements, together with an mCherry fluorescent marker and a puromycin resistance cassette under the constitutive EF1α promoter. The dual readouts (luciferase for quantitative signal, mCherry for visual confirmation of successful transduction and cell viability) make it easy to verify NFκB pathway activation in real time without the need for additional staining or lysis-based normalization controls.
This reporter line is most often deployed in inflammation, oncology, and drug discovery workflows that require sensitive monitoring of NFκB activity in a gastric cancer context. Common applications include screening small-molecule inhibitors or natural-product libraries that target upstream kinases (IKK, TAK1) or downstream regulators of the canonical NFκB cascade, evaluating the inflammatory effects of cytokines such as TNF-α, IL-1β, or LPS in a tumor-relevant background, and characterizing the crosstalk between NFκB and other oncogenic pathways active in gastric cancer. Because the line carries an mCherry internal control, it is also useful for normalization in high-content imaging, for tracking tumor cells in co-culture or invasion assays, and as a stable background for CRISPR or RNAi-based target validation studies where baseline NFκB readouts need to remain consistent across passages.
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We needed a reliable reporter system to test anti-inflammatory drugs, and this NFκB cell line performed perfectly. The luciferase induction upon TNF-alpha stimulation is significant and consistent. It was ready to use right out of the box, which streamlined our screening workflow significantly.
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