We've updated our Privacy Policy to make it clearer how we use your personal data. We use cookies to provide you with a better experience. You can read our Cookie Policy here.


Zeiss Unveils Laser Scanning Module 'DuoScan'

Listen with
Register for free to listen to this article
Thank you. Listen to this article using the player above.

Want to listen to this article for FREE?

Complete the form below to unlock access to ALL audio articles.

Read time: 1 minute

Zeiss has announced the launch of its Laser Scanning Module 'Zeiss LSM DuoScan', designed to radically expand the frontiers in live cell imaging.

The module adds a second laser scanner to the LSM 510 META or LSM 5 LIVE laser scanning microscopes. 

The dual-output, independently-adjustable lasers allow simultaneous stimulation and confocal observation while optional multi-photon microscopy preserves living tissue allowing observation without photodamage.

"Capturing fast cellular reactions occurring during or immediately after photomanipulation without a time lag will open up applications such as FRAP, FLIP, FLAP, photoactivation, photoconversion and uncaging to further development," says Aubrey Lambert, Zeiss UK marketing manager. 

"All rely on flexible sample photomanipulation to push back the frontiers of biomedical science and LSM DuoScan is the perfect partner."

The LSM DuoScan's point scanner is designed to offer a high degree of flexibility in photobleaching and can define multiple regions of interest (ROI) with pixel accuracy in all photomanipulation applications. 

This ensures that areas outside the area chosen for photobleaching are not damaged. High speed FRAP and FLIP experiments can be conducted at a variety of wavelengths, even when used with fast, parallel, multi-channel image acquisition. 

Accurate ROI micromanipulation also ensures flexibility in photoactivation, photoconversion and uncaging experiments.

Selective activation of fluorescent proteins is a further experimental possibility opened up by the LSM DuoScan photomanipulation unit.

Defined sub-populations of proteins, whole organelles or even cells in a tissue context labelled with fluorescent proteins such as PA-GFP, Dronpa or Kaede can be selectively activated or converted by local irradiation with violet light. 

Zeiss claims that, the 405-nm diode lasers, shared by the imaging and photomanipulation modules and controlled by an ROI-Bleach user interface, are ideally suited for such applications.

Two system versions of the LSM DuoScan are available: the LSM 510 META DuoScan and the LSM 5 LIVE DuoScan.