Fortis Proteinase K was tested against common competitors from various sources. They were combined with storage buffer to create a two-fold dilution series starting at a concentration of 1.25 mg/mL. Buffered reactions containing diluted enzyme were incubated for 30 minutes with a protein substrate dually labeled with FAM dye and quencher. Proteolytic cleavage of the substrate produces an increase in free fluorophore and a corresponding increase in solution fluorescence that can be measured in real-time using a microplate reader (Ex/Em = 495/520 nm).
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