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Catalog Number | orb1409943 |
---|---|
Category | Tools |
Description | Quantitatively monitor intracellular cathepsin-L activity over time in vitro. The Magic Red substrate fluoresces red upon cleavage by active cathepsin enzymes. The signal can be analyzed using fluorescence microscopy or a fluorescence plate reader. |
Target | Cathepsin L |
Application notes | 1. Prepare samples and controls, 2. Dilute cellular wash buffer 1:10 with diH2O, 3. Reconstitute FLISP with 50 µL DMSO, 4. Dilute FLISP 1:5 by adding 200 µL PBS, 5. Add 10 µL FLISP to each sample (~500 µL aliquot of cultured cells), 6. Incubate ~ 1 hour., 7. Remove media and wash cells: add wash buffer and spin cells (twice); or add fresh media and incubate 1 hour, 8. If desired, label with additional stains, such as Hoechst, PI, or an antibody, 9. If desired, fix or embed cells, 10. Analyze with a fluorescence microscope, fluorescence plate reader, or flow cytometer. FAM-FLISP excites at 488 nm and emits at 520 nm. |
Sample Types | Cell culture, tissue |
Storage | 2-8°C |
Note | For research use only |
Expiration Date | 12 months from date of receipt. |