> 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/tutorials/measure-vitroid-tm-disc/dilute-and-measure.md).

# Dilute and measure

By now the Vitroids™ disc is solubilized and a single-cell suspension is ready for BactoBox® measurements. The bacterial concentration is low so we use as little dilution factor as possible to hit the right conductivity. This is typically 1:100.  &#x20;

## How to make 1:100 dilutions

1:100 dilutions are done by transferring 101 µL sample to 10 mL of diluent.&#x20;

<figure><img src="/files/bXKclJZrqlIFfa8jFBI4" alt="" width="531"><figcaption></figcaption></figure>

### Proper vortexing of the 15 mL vial is important for reliable results

Proper vortexing of the 15 mL vials is critical. It isn't trivial. It requires a suitable vortex mixer attachment and a proper hold of the vial.

When vortexing is done correctly, a strong vortex forms in the vial within a few seconds. Follow the recommendations in the green information box and avoid the common mistakes demonstrated in the below slow-motion video (✔ demonstrates correct. ✘ demonstrates incorrect).

{% hint style="success" %}

## Good vortexing technique

<i class="fa-hashnode">:hashnode:</i> Choose a mixer platform that is compatible with your vial. [Some platforms](https://www.scientificindustries.com/collections/vortex-mixers-shakers-accessories/products/3-inch-platform-with-rubber-cover) can accommodate multiple vial types and sizes.

<i class="fa-hand-point-down">:hand-point-down:</i> Use a gentle grip on the vial cap while vortexing the tube. Start with a firm 3-finger hold on the cap and switch to a gentle press with one finger once the motion starts.
{% endhint %}

* **The left panel demonstrates proper vortexing technique:** 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.
* **The center panel demonstrates improper technique:** The vial is held too tightly using a central grip. The liquid bounces slightly, but the vortex does not form.
* **The right panel demonstrates improper technique:** A 50 mL vortex mixer attachment is used for the 15 mL tube. The vortex does not start even though the grip is correct.

<figure><img src="/files/0scSkHvpH4GTz0gw2Vpr" alt=""><figcaption></figcaption></figure>

## Step by step

{% stepper %}
{% step %}

### **Dilute 1:100 in BactoBox® diluent**

The below video demonstrates how to do a 1:100 dilution.

* Transfer 101 µL of your sample to 10 mL of diluent.
* Suspend ×10 to rinse the pipet tip for residual bacteria
* Vortex 10 seconds at maximum speed.

<figure><img src="/files/doitWovk1JoQL2ajeWLS" alt=""><figcaption></figcaption></figure>
{% endstep %}

{% step %}

### **Measure the diluted sample on BactoBox®**

The below video demonstrates how to do the bacterial measurement

* Transfer the tubing kit to the 1:100 vial.
* Press <kbd><mark style="background-color:purple;">Measure<mark style="background-color:purple;"></kbd> to start a new measurement and wait for the results.

<figure><img src="/files/aHMhf42uPfnaeswagtbo" alt=""><figcaption></figcaption></figure>
{% endstep %}

{% step %}

### Create a table of the results

Note down your results in a table.

In this example, the concentration is 89 000 cells/mL out of 130 000 total/mL. The first number is the bacterial concentration; the latter is the total objects detected in the measurement. Bacterial concentration is reported as a subset of the total objects and therefore 41 000 objects were something *other* than bacterial cells. The concentration may differ between different Vitroids™ discs.

<table><thead><tr><th width="158">Measurement ID</th><th width="121">Dilution</th><th>Cells/mL</th><th>Total/mL</th></tr></thead><tbody><tr><td><mark style="color:$info;">Q17</mark></td><td><mark style="color:$info;">100</mark></td><td><mark style="color:$info;">89 000</mark></td><td><mark style="color:$info;">130 000</mark></td></tr><tr><td></td><td></td><td></td><td></td></tr></tbody></table>

{% hint style="info" %}

## Full measurement cycle is used for samples with low bacterial concentration

Because the bacterial concentration is in the low end of the [BactoBox® working range](/advanced/advanced-sample-preparation/hit-the-right-concentration.md), the full measurement time is used.
{% endhint %}
{% endstep %}

{% step %}

### Clean the device

Transfer the tubing kit to the disinfection vial and press <kbd>Clean</kbd> .

Always run a <kbd>Clean</kbd> after running a measurement.

<figure><img src="/files/9GehlWsFhoLh8RnW6gQh" alt=""><figcaption></figcaption></figure>
{% endstep %}
{% endstepper %}

## Summary

You have now measured the cell concentration in the liquid derived from the solubilized Vitroid™ disc. In the next page, [Summary](/tutorials/measure-vitroid-tm-disc/summary.md), we will give an overview of the procedure and the obtained results.<br>

{% hint style="success" icon="laptop" %}

## Run your measurements in [Access](/software/access/access.md)

In this tutorial we keep things simple and demonstrate BactoBox® as a stand-alone-device.

But a manual log like the above table belongs to last century. Manual logs may get lost and it is common to make typing mistakes when you transfer data to spreadsheets.

[Access](/software/access/access.md) is a powerful tool to keep track of dilution factors, sample IDs and results. Data are stored on the device and can be exported easily as a csv file. See an example in [Track growth curve](/mpd/workflows/track-growth-curve.md).
{% endhint %}


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