SR-101-Phe-CMK Red FLISP Assay Kit

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. SR-FLISP excites at 590 nm and emits at 610 nm.