SYTO 82 Nuclear Staining Protocol
Nuclear stain for eukaryotic and prokaryotic cells
SYTO 82 is a cell-permeant, non-exclusive nucleic acid stain that shows a large fluorescence enhancement upon binding. In both live and dead eukaryotic cells, SYTO 82 generally shows cytoplasmic or mitochondrial as well as nuclear staining. In addition, SYTO 82 will stain most live and permeabilized bacteria.
This protocol can be used for:
- Nucleic acid (nuclear) staining in fluorescence microscopy
This protocol should not be used for:
- Flow cytometry
|1. Culture cells in an appropriate medium and vessel for fluorescence microscopy.|
|2. Remove the medium.|
|3. Wash the cells 1–3 times in a phosphate-free buffer to remove the medium.|
|4. Prepare the SYTO 82 staining solution by diluting the stock solution 1:1,000 (5 µM) in a phosphate-free buffer.|
|5. Add sufficient staining solution to cover the cells.|
|6. Incubate for 5–30 minutes, protected from light.|
|7. Remove the staining solution.|
|8. Wash sample 3 times in a phosphate-free buffer.|
|9. Image the cells.|
|Standard filter set||TRITC|
|EVOS Light Cube||RFP|
- Warm to room temperature and briefly centrifuge the DMSO solution to the bottom of the vial each time before use.
- Try multiple dye concentrations in the range from 100 nM to 5 µM to determine the optimal concentration.
- In general, the best results are obtained in buffers that do not contain phosphate, such as Hank’s Balanced Salt Solution (Cat. No. 14025092).
Cells stained with SYTO 82 dye and imaged with the Thermo Scientific™ CellInsight™ High-Content System.
For Research Use Only. Not for use in diagnostic procedures.