Customizable high density
glass arrays with well sizes
starting at 10 µm.

Interested in samples?

Please use the contact form
to get in touch with us!

Samples Available

Customizable high density
glass arrays with well sizes
starting at 10 µm.

Interested in samples?

Please use the contact form
to get in touch with us!

Samples Available

Customizable high density
glass arrays with well sizes
starting at 10 µm.

Interested in samples?

Please use the contact form
to get in touch with us!

Samples Available

Customizable high density
glass arrays with well sizes
starting at 10 µm.

Interested in samples?

Please use the contact form
to get in touch with us!

Pushing the envelope in cellomics

Next generation analytics

Stop making compromises between speed, number of experiments and cost.

With ARRALYZE^© you can perform more than 1,000,000 cellomics experiments in pico- or nanoliter glass wells on the footprint of one single microscope slide. This allows you to perform high-throughput experiments with high precision in a very economical way, using very little of expensive reagents or sparse biological samples. Glass is one of the most inert materials you can use for your biological experiment, and by using our ARRALYZE^© glass arrays you do not need to worry about chemicals leaking into your sample or some of your reagents diffusing into the matrix.

The ARRALYZE advantages at a glance

The compartmentalization of cells, DNA and other biological materials for high throughput experiments are important techniques for many reasons and droplet technology has opened up many new approaches in this context in recent years. With ARRALYZE, however, we are not only expanding the range of experiments that are possible today, but are also eliminating many of the disadvantages that droplet technology brings with it. The following table lists the main advantages of ARRALYZE compared to droplet technology:

Topic	ARRALYZE	Droplet Technology	Comments
Suppression of diffusion between compartments	✓	✖	ⓘ
No leaching of components of the matrix into the compartment	✓	✖	ⓘ
No leakage of reagents from the compartment	✓	✖	ⓘ
No risk of a fusion of compartments	✓	✖	ⓘ
Broad range of possible volumes of compartments	✓	✖	ⓘ
High flexibility regarding the composition of the compartments	✓	✖	ⓘ
Accessibility of the compartment during the experiment	✓	✖	ⓘ
Possibility to integrate anchor molecules on walls	✓	✖	ⓘ
Highly suitable for microscopic evaluation	✓	✖	ⓘ
Suitable for spheroid and micro tissue experiments	✓	✖	ⓘ
No need to use chemicals that are not required for the assay	✓	✖	ⓘ