Kit Contents
Kits include a premixed solution of AO and PI in PBS. The reagents should be stored protected from light at 2 – 8oC in an airtight container.
Assay Size | Number of Tests |
---|---|
0.25 mL | 50 |
1.5 mL | 300 |
Sample Volume and Chamber Height
The required sample volume for the CellDrop depends on the height of the measurement chamber, which is set in the counting protocol.
Standard Magnification (FLi)
Gap Height (um) | Volume (uL) | Minimum Density (cells/mL) | Maximum Density (cells/mL) |
---|---|---|---|
400 | 40 | 7.0E+02 | 3.1E+06 |
100 | 10 | 2.9E+03 | 1.3E+07 |
50 | 5 | 5.9E+03 | 2.5E+07 |
Gap Height (um) | Volume (uL) | Minimum Density (cells/mL) | Maximum Density (cells/mL) |
---|---|---|---|
400 | 40 | 4.3E+03 | 2.6E+07 |
100 | 10 | 1.7E+04 | 1.0E+08 |
50 | 5 | 3.4E+04 | 2.1E+08 |
Best Practices
- Ensure that the upper and lower chamber surfaces are clean prior to loading sample.
- Lower the arm prior to dispensing sample into the measurement chamber.
- Mix the cell suspension well immediately prior to loading sample, and avoid introducing air bubbles.
- Follow the image guides to adjust focus and fluorescence exposure.
- Allow cells to settle and stop moving across the live preview before pressing the Count button.
- Adjust exposure in the green and red channels so that fluorescent cells are not over or underexposed, as shown in the info dialog in the exposure menu.

Sample Prep
- Mix cell suspension well. Allow AO/PI to equilibrate to room temperature and vortex briefly.
- Mix AO/PI and cell suspension together in a 50% solution (1 part AO/PI + 1 part cell suspension = Dilution Factor of 2).
- Note: There is no incubation time required. Fluorescence may start to fade if cells are in AO/PI for more than 30 minutes.
- Mix sample thoroughly prior to loading onto the CellDrop.
Sample Measurement
- With the CellDrop arm in the down position, launch the AO/PI app.
- Set sample name, information and protocol as appropriate.
- Pipette well-mixed cells + AO/PI solution and dispense appropriate sample volume into the measurement chamber, using the groove on the lower sample surface as a pipetting guide.
- Note: The volume of sample required depends on the protocol settings for the chamber height. The required volume is displayed on the Count button.
- Adjust focus according to the image guide. Set initial focus in the brightfield channel, then refine focus in the green channel.
- Switch to green and red channels and adjust exposure according to the image guide.
- Allow cells to settle, then press the Count button.
Refer to Technical Note 186 – CellDrop Best Practices or Technical Note 197 – AO/PI Fluorescence Assay vs. Trypan Blue for additional guidance.
Refer to denovix.com/sds for safety data sheets for CellDrop Cell Counting Assays.
28-APR-2025