FEATURED PRODUCTS
System Principle
A new fluorescent reporter protein is formed by inserting an exogenous amino acid sequence that can be recognized and cleaved at a specific position within the green fluorescent protein without affecting the fluorescent function of the fluorescent protein.
When the inserted exogenous amino acid sequence is recognized and cleaved by protease, it directly destroys the structure of the fluorescent protein, resulting in fluorescence quenching; when the protease is inhibited by the drug, the exogenous amino acid sequence is not cleaved and fluorescence is restored, and the inhibitory effect of the inhibitor can finally be positively screened by the fluorescence value.
Simulate Real Cell Interactions
Elevate your research with our advanced system:
Dive into the forefront of cellular-level antiviral drug screening with our plasmid-based system. Say goodbye to guesswork and hello to precision in your research and development process!
Thousands of Drug Screening Capability
The system is ideal for high-throughput screening scenarios and eliminates false positives.
Seamlessly integrate with existing drug libraries and advance your research with confidence.
Our news
Stay Tuned
By clicking the button you agree to the Privacy Policy andTerms and Conditions.
