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-RR0431
Host Cell : SW620 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR0431 |
| Description | This cell line is engineered to stably overexpress GFP reporter gene. SW620 cell line is a human colon cancer cell line that has been widely used in laboratory research. This cell line is a useful tool for fluorescent tracking of SW620 cells. |
| Target Gene | GFP |
| Host Cell | SW620 |
| Host Cell Species | Homo sapiens (Human) |
| Reporter Type | Fluorescent protein |
| 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 |
In this study, the SW620-GFP cell line was utilized in a comprehensive magnetic hyperthermia experiment, spanning the entire process from the preparation of a ferrofluid containing folate-coated iron oxide nanoparticles to the execution of in vivo experiments. Physicochemical characterization of these nanoparticles revealed that they exhibit superparamagnetism, possess an average diameter of 12 ± 4 nm with a coating thickness of 2 nm, and demonstrate a high power loss density. Live SW620-GFP cells possess a unique fluorescence emission capability. This characteristic enabled researchers to rapidly analyze cell viability in vitro using epifluorescence microscopy, and to non-invasively monitor tumor size and morphology in vivo using iBox technology. Furthermore, leveraging this imaging technique, the study successfully demonstrated that administering magnetic hyperthermia three times per week over a three-week period effectively reduced tumor volume in mice.
After 24 hours of exposure to a low concentration of SPIONs (0.1 mg/mL), the relative cell viability (RCV) of SW620-GFP cells remained largely unaffected compared to the growth control group. Furthermore, even after co-incubation with higher concentrations of SPIONs (1–3 mg/mL), the RCV decreased only moderately, averaging between 73% and 85% (Figure 1a). This result confirms the low cytotoxicity of these specific SPIONs and suggests their potential suitability for use in magnetic hyperthermia (MH). For the magnetic hyperthermia treatment, SW620-GFP cells were pre-incubated with 2 mg/mL of SPIONs for 2 hours to facilitate the endocytic uptake of the nanoparticles by the cells. Subsequently, an alternating magnetic field with a frequency of 530 kHz was applied, and the temperature was maintained within a target range of 39-48 °C for 20 minutes by manually adjusting the magnetic field amplitude. The results indicated that maintaining the final temperature at ≤41 °C had virtually no negative impact on cell RCV; however, when the temperature rose to 43 °C, the RCV plummeted to less than 40% (Figure 1b). Further increases in temperature resulted in an even more pronounced decline in RCV; when the temperature reached 48 °C, cell viability was almost completely abolished, with the RCV dropping to a mere 4%. Additionally, no significant difference in RCV was observed between the two control groups, a finding attributed to the fact that the magnetic field itself does not interact with cells that have not internalized SPIONs.
Figure 1. (a) RCV of SW620-GFP cells after incubation for 24 hours in the presence of varying concentrations of SPIONs; (b) RCV of SW620-GFP cells exposed to 2 mg/mL SPIONs and heated to 39-48 °C via magnetic field irradiation. (Rosales S, et al., 2024)
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