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Myc-Luc/EF1α-mCherry Reporter Cell Line - U87MG

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

Cat. No. :   CSC-RR01131

Host Cell :   U87MG Size :   >1x106 frozen cells/vial

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Cat. No. CSC-RR01131
Description Myc-Luc/EF1α-mCherry Reporter Cell Line - U87MG
Product Type Signaling pathway reporter cell line
Target Gene Myc-Luc/EF1α-mCherry
Host Cell U87MG
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
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The Myc-Luc/EF1α-mCherry reporter cell line (based on U87MG) is a genetically engineered human glioblastoma model derived from the U87MG cell line. This cell line incorporates a reporter construct in which the Myc promoter drives the expression of firefly luciferase, enabling the quantitative monitoring of Myc transcriptional activity via bioluminescence. Additionally, an mCherry expression cassette—driven by the EF1α promoter—is integrated into the cells, serving as a constitutive fluorescent marker that facilitates the identification, visualization, and tracking of these modified cells. By combining a "pathway-responsive" luciferase readout with a stable red fluorescent signal, this dual-reporter system provides a practical and reliable platform for investigating Myc regulatory mechanisms within the context of glioblastoma.

This reporter cell line is primarily used to study the mechanisms that regulate Myc promoter activity and to assess the impact of genes, signaling pathways, chemical compounds, or biological stimuli associated with glioblastoma progression. It is well-suited for the high-throughput screening of small-molecule inhibitors or activators, assisting researchers in identifying candidate molecules capable of modulating Myc-driven transcriptional responses. The mCherry signal serves as an internal indicator of cell presence, transgene expression, and experimental consistency, while the luciferase assay allows for sensitive, quantitative measurement of promoter activity. Potential applications include drug discovery, target validation, the study of transcriptional regulation, cancer biology research, and the evaluation of combination therapeutic strategies. Given the widespread use of U87MG cells in glioblastoma research, this model can also be employed to examine cell proliferation, survival, migration, invasion, and therapeutic response, all while simultaneously monitoring Myc activity.

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Customer Reviews
Highly Efficient Tool

Monitoring Myc activity is crucial for our oncology projects, and Creative Biogene’s reporter cell line delivered exactly what we needed. The signal is highly specific, and the cell line is very stable. It has allowed us to precisely quantify how our lead candidates modulate Myc-dependent transcription in a glioblastoma context.

Canada

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