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**To calculate the number of viable cells/mL:**

- Take the average
**cell count**from each of the sets of 16 corner squares. - Multiply by 10,000 (10
^{4}). - Multiply by 5 to correct for the 1:5 dilution from the Trypan Blue addition.

In this regard, how do you count cells using a hemocytometer?

To **count cells using** a **hemocytometer**, add 15-20μl of **cell** suspension between the **hemocytometer** and cover glass **using** a P-20 Pipetman. The goal is to have roughly 100-200 **cells**/square. **Count** the number of **cells** in all four outer squares divide by four (the mean number of **cells**/square).

**total cell count**. the

**total**number of living or dead

**cells**in a given volume or area.

Secondly, how do I count a cell with text?

To **count** the number of **cells** that **contain text** (i.e. not numbers, not errors, not blank), use the **COUNTIF** function and a wildcard. In the generic form of the formula (above), rng is a range of **cells**, and "*" is a wildcard matching any number of characters. Do you want to **count cells** that **contain** specific **text**?

The **haemocytometer** is a modified and calibrated microscope slide designed to allow operators to quickly estimate the concentration of cells in a sample. The cells present in a known volume are counted and then this value converted to a number per mL.