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Dive into the research topics where Arnold Giske is active.

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Featured researches published by Arnold Giske.


Proceedings of SPIE | 2011

Confocal imaging at the nanoscale with two-color STED microscopy

Hilmar Gugel; Arnold Giske; Marcus Dyba; Jochen Sieber

STED microscopy enables confocal imaging of biological samples with a resolution that is not limited by diffraction. It provides new insights in various fields of biology, such as membrane biology, neurobiology and physiology. Its three dimensional sectioning ability allows the acquisition of high resolution image stacks. Furthermore, STED microscopy enables the recording of dynamic processes and live cell images. We present two-color imaging in confocal STED microscopy with a single STED wavelength. Pulsed and continuous wave lasers in the visible and near infra-red wavelengths range are used for stimulated emission. The resolution enhancement is demonstrated in comparison to confocal imaging with biological specimens.


Proceedings of SPIE | 2010

New developments in STED Microscopy

Arnold Giske; Jochen Sieber; Hilmar Gugel; Marcus Dyba; Dietmar Gnass

STED microscopy has gained recognition as a method to break the diffraction limit of conventional light microscopy. Despite being a new technique, STED is already successfully implemented in life science research. The resolution enhancement is achieved by depleting fluorescent markers via stimulated emission. The performance is significantly dependent on the laser source and the fluorescence markers. Therefore the use of novel fluorescent markers in conjunction with the right laser system was the main focus of our research. We present new developments and applications of STED microscopy, unraveling structural details on scales below 90nm and give an overview of required specifications for the solid state laser systems.


Proceedings of SPIE | 2012

Latest advances in commercially available STED microscopy

Wernher Fouquet; Arnold Giske

STimulated Emission Depletion (STED) microscopy enables imaging of biological samples combining significantly improved optical resolution with all benefits of confocal microscopy. Especially, by combining multi-channel image acquisition with high spatial resolution opens up a new understanding of co-localization experiments on nanoscales. Such a microscope provides new insights in various fields of biology, such as cell and membrane biology, neurobiology and physiology. We present new developments and a variety of biological examples for STED microscopy, showing structural details on scales well below 70nm and give an overview of possible field of applications, mainly focused on live cell imaging.


Archive | 2012

Scanning Microscope, and Method for Light Microscopy Imaging of a Specimen

Werner Knebel; Arnold Giske


Optics and Lasers in Engineering | 2016

Challenges in imaging cell surface receptor clusters

Rebecca Medda; Arnold Giske; Elisabetta Ada Cavalcanti-Adam


Archive | 2014

Microscope with an element for changing the shape of the illuminating light focus point

Vishnu Vardhan Krishnamachari; Arnold Giske


Archive | 2012

Phase Filters for a Scanning Microscope

Hilmar Gugel; Arnold Giske; Marcus Dyba; Roland Seifert; Bernd Widzgowski


Archive | 2017

METHOD FOR ADJUSTING THE INTENSITY OF A LIGHT BEAM IN AN OPTICAL ARRANGEMENT AND ASSOCIATED OPTICAL ARRANGEMENT

Manuel Kremer; Vishnu Vardhan Krishnamachari; Arnold Giske


Archive | 2015

Mikroskop mit einem Element zum Verändern der Form des Beleuchtungslichtfokus

Vishnu Vardhan Krishnamachari; Arnold Giske


Archive | 2013

Method and Apparatus for Investigating a Sample with Regard to the Lifetime of an Excited State

Juergen Schneider; Bernd Widzgowski; Jochen Sieber; Wernher Fouquet; Lars Friedrich; Arnold Giske; Lioba Kuschel

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