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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 4: Two-Photon Intravital Microscopy Animal Preparation Protocol to Study Cellular Dynamics in Pathogenesis
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Chapter title
Two-Photon Intravital Microscopy Animal Preparation Protocol to Study Cellular Dynamics in Pathogenesis
Chapter number 4
Book title
Light Microscopy
Published in
Methods in molecular biology, March 2017
DOI 10.1007/978-1-4939-6810-7_4
Pubmed ID
Book ISBNs
978-1-4939-6808-4, 978-1-4939-6810-7
Authors

Erinke van Grinsven, Chloé Prunier, Nienke Vrisekoop, Laila Ritsma

Editors

Yolanda Markaki, Hartmann Harz

Abstract

Two-photon intravital microscopy (2P-IVM) is an advanced imaging platform that allows the visualization of dynamic processes at subcellular resolution in vivo. Dynamic processes like cell migration, cell proliferation, cell-cell interactions, and cell signaling have an interactive character and occur in complex environments. Hence, it is of pivotal importance to study these processes in living animals, using for example 2P-IVM. 2P-IVM can be performed on a variety of tissues, from the skin of the animal to internal organs, and a variety of methods can be utilized to perform 2P-IVM on these tissues. Here, we discuss the protocols and considerations for four of those 2P-IVM methods, namely tissue explant imaging, skin imaging, surgical exposure imaging, and multi-day window imaging. We carefully compare and explain in depth how to set up each method. Lastly, in the notes section we mention some alternative solutions for the 2P-IVM methods described. In conclusion, this protocol can be used as a guide towards deciding which 2P-IVM method to use and to enable the setup of this method.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 20 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 20 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 20%
Student > Bachelor 3 15%
Researcher 2 10%
Professor > Associate Professor 2 10%
Student > Doctoral Student 1 5%
Other 4 20%
Unknown 4 20%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 20%
Agricultural and Biological Sciences 4 20%
Immunology and Microbiology 3 15%
Medicine and Dentistry 2 10%
Social Sciences 1 5%
Other 1 5%
Unknown 5 25%