Just before plating, after cold medium has been added to the trypsinized cells,
- mix 0.1 mL cell suspension with 0.1 mL 0.4% trypan blue. Live cells will not take up trypan blue. (Use a different dilution factor if cells are uncountable)
- inject 10 uL to one side of the hemocytometer (see image attached below).
- Inspect at 10x.
- Count the number of live (clear) cells in all 9 squares of the hemocyometer. (Volume = 3mm * 3 mm * 0.1 mm = 0.9 µL) (Count in 4 1mm x 1mm squares if cells are very numerous)
- Calculate the live cell concentration (# live cells * 1.11)/1µL for 9 squares,
(# live cells * 2.5/µL for 4 squares) - correct for dilution factor
