> 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-overnight-culture/dilute-and-measure.md).

# Dilute and measure

The overnight culture sample is ready for BactoBox® measurements.

An *E. coli* shake flask overnight culture typically has \~1×10<sup>10</sup> cells/mL. A 1:10,000 dilution is suitable to hit the right concentration for BactoBox® measurements. Dilution is done by two consecutive dilution steps. First a 1:100 dilution and then a 1:10 000 dilution.

## How to make 1;10,000 dilutions

Dilution is done by two consecutive dilution steps. First a 1:100 dilution and then a sequential 1:10,000 dilution.

<figure><img src="/files/04FNIoxa26Qp0DnwekUU" alt=""><figcaption></figcaption></figure>

Tutorials 1 explained the importance of using the correct vortexing technique for 15 mL vials. If you need a refresher, expand the section below. Skip ahead if you've already mastered the technique.

<details>

<summary>Proper vortex technique</summary>

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>

</details>

## Step by step

{% stepper %}
{% step %}

### Label two dilution vials

Label first dilution vial 1:100.

Label second dilution vial 1:10,000.

<figure><img src="/files/lujOkeuQgIpK8M1SWA9v" alt=""><figcaption></figcaption></figure>
{% endstep %}

{% step %}

### Dilute 1:100

Transfer 101 µL of your sample to the 1:100 vial.

Suspend ×10 to rinse the pipette tip for residual bacteria.

Vortex 10 seconds at maximum speed.

<figure><img src="/files/s4QidZEMMXv6Zrbz8WSj" alt=""><figcaption></figcaption></figure>
{% endstep %}

{% step %}

### Dilute 1:10,000

Transfer 101 µL of the 1:100 vial to the 1:10,000 vial.

Suspend ×10 to rinse the pipette tip for residual bacteria.

Vortex 10 seconds at maximum speed.

<figure><img src="/files/FGosC6OA5S7oZ0B5kizh" 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 1:10,000 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/69rlQ3SGIYgK3lAmGska" alt=""><figcaption></figcaption></figure>

{% hint style="info" icon="timeline-arrow" %}

## A measurement consists of three distinct stages

<i class="fa-square-1">:square-1:</i> First stage is **Starting up**: Conductivity and flow is checked

<i class="fa-square-2">:square-2:</i> Second stage is **Measuring**: Electric fields in the flow cell are turned on and cells are counted

<i class="fa-square-3">:square-3:</i> Third stage is **Emptying**: Pump direction is reversed and the flow path is drained.
{% endhint %}
{% endstep %}

{% step %}

### Create a table of the results

Note down your results in a table.

In this example, the concentration is 540 000 cells/mL out of 540 000 total/mL. The first number is the cell concentration; the latter is the total objects detected in the measurement. Cell concentration is reported as a subset of the total objects. The numbers are identical, i.e. all detected objects are cells.

<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:$info;">M77</mark></td><td><mark style="color:$info;">10,000</mark></td><td><mark style="color:$info;">540 000</mark></td><td><mark style="color:$info;">540 000</mark></td></tr><tr><td></td><td></td><td></td><td></td></tr></tbody></table>
{% 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 a measurement.

<figure><img src="/files/Q54ipNesb4cAXwUgDA0y" alt=""><figcaption></figcaption></figure>
{% endstep %}
{% endstepper %}

## Summary

You have now measured the cell concentration in the *E. coli* overnight culture. Notice that the BactoBox® measurement was faster here than in the first tutorial [Do a simple measurement](/tutorials/measure-vitroid-tm-disc.md). The <i class="fa-forward">:forward:</i> **fast results** feature is triggered because the bacterial concentration in the diluted sample was higher.

In the next page, [Summary](/tutorials/measure-overnight-culture/summary.md), we will give an overview of the procedure and the obtained results.

{% 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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