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Light Microscopy

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Cover of 'Light Microscopy'

Table of Contents

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    Book Overview
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    Chapter 1 Introduction to Modern Methods in Light Microscopy
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    Chapter 2 Three-Dimensional Live Imaging of Filamentous Fungi with Light Sheet-Based Fluorescence Microscopy (LSFM)
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    Chapter 3 Light-Sheet Fluorescence Microscopy: Chemical Clearing and Labeling Protocols for Ultramicroscopy
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    Chapter 4 Two-Photon Intravital Microscopy Animal Preparation Protocol to Study Cellular Dynamics in Pathogenesis
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    Chapter 5 Imaging of Brain Slices with a Genetically Encoded Voltage Indicator
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    Chapter 6 FRET Microscopy for Real-Time Visualization of Second Messengers in Living Cells
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    Chapter 7 Imaging the Dynamics of Cell Wall Polymer Deposition in the Unicellular Model Plant, Penium margaritaceum
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    Chapter 8 Targeted Ablation Using Laser Nanosurgery
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    Chapter 9 Sample Preparation and Choice of Fluorophores for Single and Dual Color Photo-Activated Localization Microscopy (PALM) with Bacterial Cells
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    Chapter 10 STED Imaging in Drosophila Brain Slices
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    Chapter 11 Two-Color Total Internal Reflection Fluorescence Microscopy of Exocytosis in Endocrine Cells
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    Chapter 12 Optical Coherence Microscopy
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    Chapter 13 Designing Image Analysis Pipelines in Light Microscopy: A Rational Approach
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    Chapter 14 Automated Analysis of Intracellular Dynamic Processes
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    Chapter 15 Quantitative Image Analysis of Single-Molecule mRNA Dynamics in Living Cells
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    Chapter 16 Analysis of Protein Kinetics Using Fluorescence Recovery After Photobleaching (FRAP)
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    Chapter 17 Fluorescence-Based High-Throughput and Targeted Image Acquisition and Analysis for Phenotypic Screening
Attention for Chapter 3: Light-Sheet Fluorescence Microscopy: Chemical Clearing and Labeling Protocols for Ultramicroscopy
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Chapter title
Light-Sheet Fluorescence Microscopy: Chemical Clearing and Labeling Protocols for Ultramicroscopy
Chapter number 3
Book title
Light Microscopy
Published in
Methods in molecular biology, March 2017
DOI 10.1007/978-1-4939-6810-7_3
Pubmed ID
Book ISBNs
978-1-4939-6808-4, 978-1-4939-6810-7
Authors

Nina Jährling, Klaus Becker, Saiedeh Saghafi, Hans-Ulrich Dodt

Editors

Yolanda Markaki, Hartmann Harz

Abstract

Light-sheet microscopy is an effective technique in neuroscience, developmental biology, and cancer research for visualizing and analyzing cellular networks and whole organs in three dimensions. Because this technique requires specimens to be translucent they commonly have to be cleared before microscopy inspection. Here, we provide 3DISCO based protocols for preparing cleared samples of immuno-stained neural networks, lectin-labeled vascular networks, and Methoxy-X04 labeled beta-amyloid plaques in mice. 3DISCO utilizes the lipophilic solvents tetrahydrofuran (THF) and dibenzylether (DBE) for dehydration and successive clearing. Crucial steps for obtaining transparent tissues and preserving the fragile endogenous GFP are the transcardial perfusion, as well as the proper implementation of the 3DISCO clearing process using peroxide free chemicals. We further provide a protocol for resin embedding of 3DISCO cleared specimens that allows long term archiving of samples for years with virtually no loss in signal quality.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 31 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 31 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 10 32%
Student > Bachelor 6 19%
Student > Ph. D. Student 5 16%
Professor > Associate Professor 3 10%
Student > Doctoral Student 1 3%
Other 5 16%
Unknown 1 3%
Readers by discipline Count As %
Medicine and Dentistry 8 26%
Neuroscience 7 23%
Biochemistry, Genetics and Molecular Biology 4 13%
Agricultural and Biological Sciences 3 10%
Engineering 3 10%
Other 3 10%
Unknown 3 10%