Scepter Cell Counting Technology The Coulter Principle

The Scepter Cell Counting technology is using the Coulter Principle

The gold standard counter is smaller than ever! The Scepter cell counter uses the Coulter principle of impedance-based particle detection to reliably and accurately count every cell in your sample.


Discover how Scepter works, Step-by-Step Protocol


Sample Preparation Cell Count Gating Process Exporting & Manipulating Data

Sample Preparation

Start with a single-cell suspension, diluted to a total volume of 100 µL (recommended) in phosphate buffered saline (such as EmbryoMax® 1x DPBS) to 10,000-500,000 cells/mL (operating range) in a 1.5 mL microcentrifuge tube.

Counting Process

The sensing zone also measures cell sizes and cell volumes with sub-micron and sub-picoliter resolution, enabling the Scepter cytometer to display a histogram distribution of cell size or cell volume.


The Scepter cell counter displays each step of the cell counting protocol
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Gating Process

Once counting is complete, you can click the control button and scroll to manually adjust the upper and lower gates. After gating, you will see recalculated data displaying a new concentration, average cell size and volume. Gating allows you to look only at the population of cells you are interested in.


The enhanced embedded software of the Scepter cell counter helps you better interpret your cell counting data
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Exporting and Manipulating Data

Store up to 72 histograms on the Scepter cell counter itself, or upload data to your personal computer using the included software and USB cable. The Scepter Application Software shows uploaded volume and size distribution data as shown below. Easily share your data or conduct in-depth analysis by exporting uploaded files to Microsoft Excel.

The Scepter 2.0 Software Pro user interface has 5 main components:

You can easily manipulate your cell counting data using the Scepter™ 2.0 Software Pro
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