Use of haemocytometer to quantify concentration of cells' suspensions
abotero
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Abstract
This protocol presents the procedures to estimate the concentration of cells' suspensions using an hemocytometer
Steps
Wash the hemocytometer with a washer bottle and dry it using a paper towel
Cover the hemocytometer with the coverslip and place it on a flat surface
Vortex briefly the cell suspension whose concentration will be calculated
Using a micropipette collect 10-100 µl of the previously agitated suspension
Place the micropipette tip on the hemocytometer edge near the coverslip
Empty the spore suspension slowly into the chamber of the hemocytometer
Place the hemocytometer in the microscope's mechanical stage and secure it using the stage clip
Turn on the microscope and focus on the hemocytometer
Look out for the first square to be counted
Count the number of cells on each square
Write down the number of cells on each square
If cells were counted on squares of size 1
Concentration (cells/ml)= Number of counted cells*10,000/Number of squares counted
If cells were counted on squares of size 2
Concentration (cells/ml)= Number of counted cells*160,000/Number of squares counted
If cells were counted on squares of size 3
Concentration (cells/ml)= Number of counted cells*250,000/Number of squares counted