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30<br />

Microscopy<br />

Core Facility<br />

Andreas Vonderheit<br />

Education<br />

2000 Diploma in Molecular Biology, ZMBH, University of Heidelberg<br />

2004 PhD in Biochemistry, ETH, Zürich<br />

Positions held<br />

2005-2008 Postdoctoral Researcher, Institute of Nanotechnology, ETH, Zürich<br />

2008-2011 Screening Scientist at the RNAi Image-based Screening Center (RISC)<br />

at the Light Microscopy Centre (LMC), ETH, Zürich<br />

Since 2011 Head of Microscopy, Core Facilities and Technology,<br />

Institute of Molecular Biology (<strong>IMB</strong>), Mainz<br />

Core Facility Overview<br />

The Microscopy Core Facility not only provides hands-on training and<br />

access to various state-of-the-art microscopes, but also offers further<br />

education through the provision of a variety of practical courses and<br />

lectures. Training lectures provided range from a general “Introduction<br />

to Microscopy” to “Pitfalls in Image Acquisition” and “Ethics in Image<br />

Acquisition and Processing”. Lectures, courses and the scientific services<br />

available are all open to Mainz’ scientific community. To date the lectures<br />

have attracted a large number of non-<strong>IMB</strong> researchers, with about<br />

80% of the audience coming from Johannes Gutenberg University<br />

and the University Medical Center. The microscopes provided are<br />

utilized equally by <strong>IMB</strong> staff and external users.<br />

Services Offered<br />

The facility provides hands-on training and access to various ultramodern<br />

confocal laser scanning microscopes, super-<strong>resolution</strong> microscopes<br />

and motorized fast-flourescence microscopes for live-cell<br />

microscopy. There are also PCs for image processing equipped with<br />

software for deconvolution and 3D-rendering. The following microscopic<br />

equipment, a large part of which was financed by DFG, is available:<br />

• M80 Demonstration Stereo Microscope: Equipped with a camera<br />

and a 24“ monitor for teaching<br />

• M205 FA Fluorescence Stereo Microscope: Equipped with a<br />

camera, fluorescence light source and three filters for UV, green,<br />

and red fluorophores<br />

• DM2500 Fluorescence Upright Microscope: Equipped with a<br />

colour camera, fluorescence light source and three filters for UV,<br />

green, and red fluorophores and with five air objectives (this microscope<br />

is perfectly suited for histology)<br />

• AF7000 Widefield Fluorescence Microscope: This widefield microscope<br />

is equipped with an incubator box for live-microscopy, fast<br />

filter wheels and a fast camera<br />

• TCS LSI Macro Zoom Confocal: This microscope combines a stereo<br />

microscope with a confocal. Organisms like C. elegans or Drosophila<br />

larvae can be scanned as a whole or zoomed down to single<br />

cell level in confocal mode<br />

• TCS SPE Confocal Microscope: An upright confocal microscope<br />

with one detector<br />

• TCS SP5 Confocal Microscope: An inverse microscope with four<br />

PMTs, four lasers, and a fast resonance scanner<br />

• TCS STED CW Super-Resolution Microscope: A super-<strong>resolution</strong><br />

microscope which allows live microscopy and FCS. Equipped with<br />

an incubation box, two normal PMTs and two HyD detectors<br />

• SR GSD Super-Resolution Microscope (localization method):<br />

A super-<strong>resolution</strong> microscope on which TIRF is possible<br />

• Image Processing Station<br />

Figure 1. Mitochondria network in CHO cells labeled with Mitotracker® and imaged with<br />

a confocal microscope. (A) One plane of a z-stack. (B) Same plane after deconvolution. (C)<br />

Cutout of A. (D) Cutout of B. Scalebar: 4 µm. Imaged by A. Vonderheit.

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