Automated spinning disk confocal microscopy in 3D live cell imaging

Warning

This publication doesn't include Faculty of Arts. It includes Faculty of Informatics. Official publication website can be found on muni.cz.
Authors

VAŘECHA Miroslav MATULA Pavel KOZUBEK Michal

Year of publication 2010
Type Conference abstract
MU Faculty or unit

Faculty of Informatics

Citation
Description Fluorescence microscopy has become the leading technology to study structure and dynamics of cellular components and processes. Fluorescent proteins allow us to study protein dynamics, localization, and interactions in living cells. In our laboratory, we have been developing special systems for automated cell image acquisition and analysis using fluorescence microscopy working up to five dimensions (x, y, z, t, lambda), whose hardware and software was optimized for studies on living cells. The presentation will focus on the latest developments in our technology. Besides microscopy hardware and software, also examples of possible applications will be presented. For the first time, we discovered interaction of apoptotic proteins AIF and endonuclease G, expressed using one DNA plasmid, in living human cells during apoptotic cell death.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.