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-RR00831
Host Cell : SiHa Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR00831 |
| Description | This cell line is engineered to stably express GFP reporter gene in SIHA cells. It is an ideal cell line model in fluorescent tracking of SIHA cells. |
| Product Type | Stable cell line constitutively expressing GFP reporter gene |
| Target Gene | GFP |
| Host Cell | SiHa |
| Host Cell Species | Homo sapiens (Human) |
| Applications |
1) in vitro cell tracking by fluorescent signal 2) monitor in vivo tumor growth using the fluorescence 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) cell line imaging under fluorescent microscopy 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 |
| Target Gene | GFP |
SIHA cells are a human cervical squamous cell carcinoma–derived cell line widely used as an in vitro model for studying cervical cancer biology and HPV-associated oncogenic transformation. These cells exhibit epithelial morphology, robust proliferative capacity, and molecular characteristics typical of high-grade cervical carcinoma, including dysregulation of cell cycle control, apoptosis resistance, and enhanced invasive potential. SIHA cells are particularly valuable for investigating the molecular mechanisms underlying HPV-driven carcinogenesis and tumor progression in cervical epithelial tissues. The GFP Reporter Cell Line – SIHA is generated by stable integration of a green fluorescent protein (GFP) reporter construct driven by pathway-responsive promoters or transcription factor–specific regulatory elements into the parental SIHA background, enabling real-time visualization and quantitative analysis of cellular signaling activity and gene expression while preserving the intrinsic biological features of the original cell line.
The GFP Reporter Cell Line – SIHA is widely applied in cervical cancer research, HPV-related signaling studies, and live-cell imaging–based drug screening. Unlike luciferase-based systems, the GFP reporter allows direct fluorescence-based detection of cellular activity, enabling real-time monitoring of dynamic biological processes at the single-cell level without substrate addition. This model is particularly useful for studying key signaling pathways involved in cervical carcinogenesis, including PI3K/AKT, MAPK/ERK, NF-κB, Wnt/β-catenin, and JAK/STAT pathways, as well as HPV-mediated regulatory mechanisms affecting cell proliferation and survival. The GFP signal provides a stable and non-invasive readout suitable for high-content imaging, time-lapse microscopy, and quantitative fluorescence analysis. This cell line is commonly used in compound screening, mechanistic studies of tumor progression, and evaluation of gene regulation dynamics, making it a valuable tool for both basic research and translational studies in cervical cancer biology.
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We purchased the SIHA GFP reporter line for our HPV-related cervical cancer studies, and it has been outstanding. The GFP expression is bright, uniform, and stable — we consistently see >95% GFP-positive cells by flow cytometry even after multiple passages.
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