Transfected Stable Cell Lines
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Cat. No. : CSC-RR00660
Host Cell : AGS Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR00660 |
| Description | AGS-Luc reporter cell line is engineered to stably express Luciferase reporter gene in AGS cell line. |
| Target Gene | Luciferase |
| Host Cell | AGS |
| Host Cell Species | Homo sapiens (Human) |
| Applications |
1. Gene expression studies 2. Protein localization 3. Drug screening and toxicology 4. Live cell imaging |
| Size | >1x106 frozen cells/vial |
| Stability | Validated for at least 10 passages |
| Quality Control | Negative for bacteria, yeast, fungi and mycoplasma. |
| 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. |
| 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 |
| Target Gene | Luciferase |
The AGS-Luciferase Reporter Cell Line (AGS-Luc) is a stable reporter cell model generated by integrating a luciferase reporter gene into the AGS human gastric adenocarcinoma cell line to achieve constitutive expression. AGS cells are a widely used epithelioid gastric cancer cell line derived from human gastric adenocarcinoma; they are frequently employed in research areas such as gastric tumor biology, host-pathogen interactions, epithelial cell signaling, drug responses, and the mechanisms of cancer progression. Because AGS cells retain key characteristics of gastric epithelial tumor cells, they provide a practical in vitro platform for studying pathways associated with gastric cancer. In the AGS-Luc reporter cell line, the luciferase gene is stably integrated into the AGS genome, enabling the cells to constitutively express luciferase.
This cell product is suitable for a wide range of applications in gastric cancer research and reporter-based biological assays. A primary application is the assessment of cell viability, proliferation, and cytotoxicity; in these experiments, changes in the luminescent signal allow for the rapid, quantitative monitoring of cell growth or the inhibitory effects of anti-cancer compounds. The AGS-Luc reporter cell line is also well-suited for drug screening programs, including the evaluation of small-molecule drugs, natural products, targeted therapies, chemotherapeutic agents, and combination treatment strategies against gastric cancer. Given the high sensitivity of luciferase assays and their compatibility with multi-well plate formats, this cell line supports medium- to high-throughput screening workflows. Another significant application lies in tumor xenograft studies: following the implantation of AGS-Luc cells into immunodeficient mice, tumor growth and metastasis can be monitored non-invasively using bioluminescence imaging technology.
In this study, researchers investigated the feasibility of utilizing Isosulfan Blue (IB) for the visualization of sentinel lymph nodes (SLNs) in mouse models of gastric cancer (GC). In an ectopic gastric tumor implantation model, AGS-luciferase (AGS-Luc) cells were inoculated into the right hind footpads of nude mice (tumor group), while the left hind footpads served as controls (normal group). When the tumor volume in the footpads reached approximately 250 mm³, a 1% IB solution was injected into the tissue surrounding the tumors. In an orthotopic gastric tumor model, AGS-Luc cells were injected into the subserosal layer of the stomach. Once metastatic SLNs were detected via in vivo imaging, a 1% IB solution was injected into the gastric subserosa of the nude mice.
The results demonstrated that the mean staining times for the popliteal lymph nodes (LNs) in the tumor and normal groups were 21.48 ± 10.41 s and 33.30 ± 16.79 s, respectively. The mean fading times for the popliteal LNs in the two groups were 79.39 ± 21.95 min and 85.24 ± 16.44 min, respectively. In the orthotopic gastric tumor model, following the injection of IB, SLNs were macroscopically visible to the naked eye under standard indoor lighting conditions; the mean staining time for the SLNs was 104.0 ± 23.34 s, with a detection rate of 60%. Regarding metastatic LNs, the presence of metastasis in both the ectopic and orthotopic tumor models was confirmed via Hematoxylin-Eosin (HE) staining. These findings indicate that the use of IB for lymphatic mapping is both feasible and effective. The concept of IB-based sentinel lymph node mapping demonstrates feasibility in mouse models and holds promise for potential application in the clinical management of gastric cancer.
Figure 1. Visualization of blue-stained popliteal lymph nodes. (Zhu, Xudong, et al., 2025)
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We used the Luciferase Reporter Cell Line - AGS for gastric cancer-related assays and were pleased with its performance. The luminescence readings were clear and consistent, allowing us to evaluate experimental conditions efficiently. This cell line has become a useful part of our workflow.
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