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This kit enables simultaneous determination of live and dead cells with two probes: CellTrace calcein violet indicates cell viability based on plasma membrane integrity, and aqua-fluorescent reactive dye measures cell vitality based on intracellular esterase activity.
1. Thaw one vial each of components A, B, and C |
2. Add 50 μL DMSO (Component C) to one vial of aqua-fluorescent reactive dye (Component B) |
3. Add 42 μL DMSO (Component C) to one vial of calcein violet AM (Component A) to prepare a stock solution |
4. Add 40 μL of this stock solution to 1.25 mL of buffer or medium to make a working solution of calcein violet AM |
5. Add 1 mL cells to a flow cytometer tube. Cells may be suspended in serum-free medium or buffer |
6. Add 1 μL aqua-fluorescent reactive dye working solution and 5 μL calcein violet AM working solution to each mL cell suspension |
7. Mix the sample |
8. Incubate the cells for 30 minutes at room temperature or on ice |
9. Wash once and resuspend in buffer |
10. Run cells on a flow cytometer using violet (~405 nm) excitation and violet fluorescence emission (~450 nm) for the calcein violet (live cells) and blue-green fluorescence emission (~525 nm) for the aqua-fluorescent reactive dye (dead cells); minimal compensation will be necessary |
Staining pattern of a mixture of heat-killed and untreated Jurkat cells (human leukemia T-cell) stained with the LIVE/DEAD Violet Viability/Vitality Kit.
Aqua-fluorescent reactive dye | Calcein violet AM | |
---|---|---|
Excitation/Emission | 367/526 nm | 400/452 nm |
Storage conditions | –20°C | –20°C |