We offer over a dozen web tools to educate researchers on fluorophores, build the ideal multicolor panel, and choose the right reagents for flow cytometry applications. For additional inquiries, contact our Technical Services team.
We offer over a dozen web tools to educate researchers on fluorophores, build the ideal multicolor panel, and choose the right reagents for flow cytometry applications. For additional inquiries, contact our Technical Services team.
“Conventional/traditional” flow cytometers use a series of mirrors and filters in order to capture the emission wavelengths from excited fluorophores. Fluors that have emission profiles that fall into the same filter cannot be separated or identified from one another.
Our spectra analyzer can display the excitation and emission spectra for dozens of fluorophores. This allows you to compare the excitation and emission profiles of fluors, custom filters, and laser lines to see what best fits your cytometer.
Spectral cytometers capture the full spectrophotometric profile of the fluorophores across all lasers. The fluors’ profiles are captured in 10-30 nm segments across the emission range to accurately unmix the fluorophores. This allows fluors that normally cannot be unmixed on a conventional cytometer (e.g. Pacific Blue™ and Brilliant Violet 421™) to be used together on an instrument like Cytek’s Aurora.
As such, this web tool is dedicated to displaying the emission spectra of fluorophores based on Cytek’s Aurora spectral cytometers.
The SONY ID7000 Spectral Cell Analyzer can be configured with up to 7 lasers and 186 detectors and features an adaptable Spectral Reference Library and Autofluorescence Finder to enable streamlined experiment setup and quality multi-parameter data in user-friendly workflows.
A comparison of channels that might typically be used for the violet laser on a spectral cytometer (top) compared to filters on a conventional cytometer (bottom). The added “side-by-side” channels on a spectral cytometer allow spectrally similar fluors to be unmixed depending on how their emission profiles look in other channels (including the ones available on additional lasers). On a conventional cytometer, a fluor’s main ‘peak’ or emission is mainly captured in one filter set, making it harder to distinguish spectrally similar fluors.
Follow Us