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  2. To stain live cells, you can follow the following protocol1:
    1. Add the dye to complete culture medium. We recommend using Hoechst dyes at 1 ug/mL or DAPI at 10 ug/mL.
    2. Remove culture medium from the cells and replace with medium containing dye.
    3. Incubate cells at room temperature or 37°C for 5-15 minutes, then image. Note: Washing is not necessary for specific staining, but nuclear staining is stable after washing.
    Alternatively, you can fix the cells with 4% formaldehyde (diluted in 1X PBS) for 10 min at room temperature2.
    Learn more:

    Considerations for Staining Live Cells

    • Add the dye to complete culture medium. We recommend using Hoechst dyes at 1 ug/mL or DAPI at 10 ug/mL. ...
    • Remove culture medium from the cells and replace with medium containing dye.
    biotium.com/tech-tips/protocol-staining-cells-with-h…

    Staining protocol 1. Discard the cell culture medium by inverting the slide and gently tapping it on a paper towel to remove the remaining medium. 2. ™Fix the cells with 4% formaldehyde (diluted in 1X PBS— prepare fresh) for 10 min at room temperature (fixation time can be increased to 20 min depending on the cell line).

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