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GFP Reporter Stable Cell Line-HeLa

For research use only. Not intended for any clinical use.

Cat. No. :   CSC-RR0047

Host Cell :   HeLa Size :   >1x106 frozen cells/vial

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Cat. No. CSC-RR0047
Description This cell line is engineered to stably overexpress the GFP in HeLa cells.
Introduction The green fluorescent protein (GFP) is a protein composed of 238 amino acid residues (26.9kDa) that exhibits bright green fluorescence when exposed to light in the blue to ultraviolet range. Although many other marine organisms have similar green fluorescent proteins, GFP traditionally refers to the protein first isolated from the jellyfish Aequorea victoria. The GFP from A. victoria has a major excitation peak at a wavelength of 395 nm and a minor one at 475 nm. Its emission peak is at 509 nm, which is in the lower green portion of the visible spectrum. The fluorescence quantum yield (QY) of GFP is 0.79. The GFP from the sea pansy (Renilla reniformis) has a single major excitation peak at 498 nm.
Target Gene GFP
Abbr Hela-GFP
Host Cell HeLa
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.
Morphology Epithelial
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
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HeLa is the oldest and most widely used immortalized human cell line, originally isolated in 1951 from a cervical adenocarcinoma biopsy taken from Henrietta Lacks. These epithelial cells grow adherently with a doubling time of roughly 20 to 24 hours and are known for their remarkable durability and prolific nature in culture. The HeLa karyotype is hypertriploid, typically containing 76 to 80 chromosomes, and the cells carry integrated human papillomavirus type 18 sequences. The GFP Reporter Stable Cell Line-HeLa is a genetically modified derivative that stably expresses green fluorescent protein under the control of a constitutive or inducible promoter. This engineered line was generated through transfection and antibiotic selection to create a homogeneous population that consistently produces GFP, enabling real-time visualization of cellular events without the need for repeated transfection or staining steps.

This stable reporter cell line is widely used in drug screening, gene expression analysis, and signal transduction studies. Because GFP fluorescence can be monitored live and non-invasively, researchers can track changes in promoter activity, protein localization, or cell behavior over time in a high-throughput format. The line is particularly valuable for testing compounds that modulate transcriptional activity, as GFP intensity serves as a direct readout of pathway activation or inhibition. It also supports applications in virology, where GFP expression allows rapid detection of viral infection or replication kinetics. In cancer biology, these cells are used to study tumor cell proliferation, migration, and response to therapeutic agents in both 2D and 3D culture models. The stable integration of the GFP reporter eliminates the variability associated with transient transfection, making this cell line a reliable and reproducible tool for long-term experiments and large-scale screening campaigns.

High-risk human papillomavirus (HPV) infections not only cause cervical cancer, but have also been linked to the development of anogenital cancers as well as head and neck cancers. Researchers combined HPV E6/E7 siRNA with chemotherapeutic agents to analyze their synergistic effects in TP53 and RB/E2F signaling, cell proliferation and apoptosis. Through in vitro and in vivo experiments, it was found that the combination of E6/E7 siRNA and cisplatin restored TP53 and RB/E2F signaling more effectively than E6/E7 siRNA alone and led to apoptosis or cell cycle arrest. The researchers also developed a cellular kinetic model incorporating TP53-RB/E2F dynamics and cell proliferation characteristics, validating its utility in studying the E6/E7 siRNA combination treatment regimen. The interaction between TP53 and RB/E2F signaling mechanisms was further confirmed using a dual reporter system. Ultimately, by injecting BALB/c nude mice with E6/E7 siRNA cationic liposomes combined with cisplatin and paclitaxel, the researchers found that this combination therapy significantly inhibited tumor growth. In summary, the combination of E6/E7 siRNA and low-dose chemotherapy can effectively inhibit tumor growth by stabilizing TP53 and the RB/E2F inhibitory complex.

The graph depicts the dynamics of TP53-RE-GFP and E2F-RE-RFP under HPV E6/E7 siRNA treatment alone or in combination with CDDP. (doi: 10.1016/j.neo.2017.07)Figure 1. Researchers evaluated the growth characteristics and TP53 recovery of TP53-RE-GFP-stabilized cells transfected with HPV E6/E7 siRNA or control siRNA using the IncuCyte HD System (Essen Instruments, Ann Arbor, MI). Detailed setup procedures are listed in Supplementary Materials and Methods. Researchers analyzed TP53-RE-GFP dynamic time series in TP53-RE-GFP reporter HeLa stable cells treated with NC plus cisplatin (CDDP), SP, or SP plus CDDP. (Rajasekaran N, et al., 2017)

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Customer Reviews
Real time observability.

One significant advantage of using GFP Reporter Stable Cell Line HeLa to cultivate cell lines is the ability to observe gene or protein expression in real-time. Through a fluorescence microscope, I can clearly see which regions or cells are expressing the genes or proteins that interest me. This has provided great convenience for my experiment and also gave me a deeper understanding of the experimental results.

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