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Microscopy Research and Technique
Article . 2018 . Peer-reviewed
License: Wiley Online Library User Agreement
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Technical implementations of light sheet microscopy

Authors: Zagato Elisa; Brans Toon; Stefaan C. De Smedt; Remaut Katrien; Neyts Kristiaan; Braeckmans Kevin;

Technical implementations of light sheet microscopy

Abstract

AbstractFluorescence‐based microscopy is among the most successful methods in biological studies. It played a critical role in the visualization of subcellular structures and in the analysis of complex cellular processes, and it is nowadays commonly employed in genetic and drug screenings. Among the fluorescence‐based microscopy techniques, light sheet fluorescence microscopy (LSFM) has shown a quite interesting set of benefits. The technique combines the speed of epi‐fluorescence acquisition with the optical sectioning capability typical of confocal microscopes. Its unique configuration allows the excitation of only a thin plane of the sample, thus fast, high resolution imaging deep inside tissues is nowadays achievable. The low peak intensity with which the sample is illuminated diminishes phototoxic effects and decreases photobleaching of fluorophores, ensuring data collection for days with minimal adverse consequences on the sample. It is no surprise that LSFM applications have raised in just few years and the technique has been applied to study a wide variety of samples, from whole organism, to tissues, to cell clusters, and single cells. As a consequence, in recent years numerous set‐ups have been developed, each one optimized for the type of sample in use and the requirements of the question at hand. Hereby, we aim to review the most advanced LSFM implementations to assist new LSFM users in the choice of the LSFM set‐up that suits their needs best. We also focus on new commercial microscopes and “do‐it‐yourself” strategies; likewise we review recent designs that allow a swift integration of LSFM on existing microscopes.

Country
Belgium
Related Organizations
Keywords

light sheet microscopy, SELF-RECONSTRUCTING BEAMS, FLOW-CYTOMETRY, FLUORESCENCE MICROSCOPY, Biology and Life Sciences, PLANE ILLUMINATION MICROSCOPY, CROSS-CORRELATION SPECTROSCOPY, SPIM, CELL 3D SUPERRESOLUTION, Medicine and Health Sciences, HIGH-SPEED, ZEBRAFISH DEVELOPMENT, BESSEL BEAMS, THICK BIOLOGICAL SAMPLES

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    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 10%
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
39
Top 10%
Top 10%
Top 10%
Green
bronze