> For the complete documentation index, see [llms.txt](https://help.sbtinstruments.com/llms.txt). Markdown versions of documentation pages are available by appending `.md` to page URLs; this page is available as [Markdown](https://help.sbtinstruments.com/measurement-essentials/simple-measurement.md).

# Always disaggregate

BactoBox® is a flow cytometer. This means that cells are counted individually as they pass through the detector. For the most reliable results, disaggregate cell clumps into a single-cell suspension before measurement.

<div data-with-frame="true"><figure><img src="/files/eG1tkOh0hvAdjZl5v60O" alt=""><figcaption><p>Single cells can readily enter the measurement channel, while larger clumps of cells must be disaggregated prior to dilution and measurement. Otherwise underestimation of cells may occur.</p></figcaption></figure></div>

## How to get a single-cell suspension

The best way to disaggregate cells is to use a mechanical method when the cells are still in the growth medium.

<figure><img src="/files/KfFU2FVNVU41hY7b8Lja" alt=""><figcaption><p>Vortex at maximum speed for 1 minute in a small vial like a 2 mL or 5 mL Eppendorf tube.</p></figcaption></figure>

## Master the art of vortexing

Vortexing may look simple. It isn't. Especially not for larger vials. Proper vortexing requires a suitable vortex mixer attachment and a proper hold of the vial.

<figure><img src="/files/0scSkHvpH4GTz0gw2Vpr" alt=""><figcaption><p>Slow-motion vortexing of a 15 mL vial. Left: correct grip and correct attachment. Center: too tight grip. Right: wrong attachment.</p></figcaption></figure>

{% columns %}
{% column %}

<p align="center"><strong>Correct</strong> <i class="fa-check">:check:</i></p>

The cap is initially held with three fingers to start the motion, after which a single finger applies light downward pressure while allowing the tube to vortex freely.
{% endcolumn %}

{% column %}

<p align="center"><strong>Incorrect</strong> ✘</p>

The vial is held too tightly using a central grip. The liquid bounces slightly, but the vortex does not form.
{% endcolumn %}

{% column %}

<p align="center"><strong>Incorrect</strong> ✘</p>

A 50 mL vortex mixer attachment is used for the 15 mL tube. The vortex does not start even though the grip is correct.
{% endcolumn %}
{% endcolumns %}

## Learn the ropes

This mini course provided you with the essentials on how to disaggregate cell clumps prior to BactoBox® measurements.

Try our first tutorial for a quick, hands-on example on how to disaggregate cell clumps.

{% content-ref url="/pages/yOiWxVnPgOuX7cibH9R9" %}
[Do a simple measurement](/tutorials/measure-vitroid-tm-disc.md)
{% endcontent-ref %}

Proceed to the next mini-course [Hit the right concentration](/measurement-essentials/hit-the-right-concentration.md) to learn why cultures must be diluted prior to measurements.


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