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Confocal Microscopy

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Cover of 'Confocal Microscopy'

Table of Contents

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    Book Overview
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    Chapter 1 Reflecting on Confocal Microscopy: A Personal Perspective
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    Chapter 2 Laser Scanning Confocal Microscopy: History, Applications, and Related Optical Sectioning Techniques
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    Chapter 3 Confocal microscopy on the internet.
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    Chapter 4 Using Photoshop with Images Created by a Confocal System
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    Chapter 5 Clearing Up the Signal: Spectral Imaging and Linear Unmixing in Fluorescence Microscopy
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    Chapter 6 Low Magnification Confocal Microscopy of Tumor Angiogenesis
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    Chapter 7 Confocal imaging of butterfly tissue.
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    Chapter 8 Confocal Microscopy of Cardiac Myocytes
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    Chapter 9 Confocal imaging of fluorescently labeled proteins in the Drosophila larval neuromuscular junction.
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    Chapter 10 Confocal imaging and three-dimensional visualization of thick autofluorescent specimens.
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    Chapter 11 Vital Imaging of Multicellular Spheroids
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    Chapter 12 Live confocal analysis of mutant- and drug-treated Drosophila embryos.
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    Chapter 13 Confocal Imaging of the Microtubule Cytoskeleton in C. elegans Embryos and Germ Cells
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    Chapter 14 Measurement in the Confocal Microscope
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    Chapter 15 A Method for Quantifying Blood Flow Distribution Among the Alveoli of the Lung
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    Chapter 16 Imaging Tools for Analysis of the Ureteric Tree in the Developing Mouse Kidney
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    Chapter 17 Evaluating Confocal Microscopy System Performance
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    Chapter 18 Erratum
Attention for Chapter 9: Confocal imaging of fluorescently labeled proteins in the Drosophila larval neuromuscular junction.
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Chapter title
Confocal imaging of fluorescently labeled proteins in the Drosophila larval neuromuscular junction.
Chapter number 9
Book title
Confocal Microscopy
Published in
Methods in molecular biology, January 2014
DOI 10.1007/978-1-60761-847-8_9
Pubmed ID
Book ISBNs
978-1-58829-351-0, 978-1-60761-847-8
Authors

Ian P Coyle, Ian P. Coyle, Coyle, Ian P.

Abstract

The Drosophila larval neuromuscular junction (NMJ) consists of a presynaptic motor neuron terminal and a postsynaptic muscle cell that offer an accessible and popular model system for the analysis of synaptic growth and function. I describe techniques for visualizing fluorescently labeled proteins within dissected, formaldehyde-fixed second to third instar larval NMJs. In addition, I present two strategies using confocal microscopy to solve a particular problem in NMJ analysis: distinguishing fluorescence in the presynaptic nerve terminal from that in the adjacent postsynaptic muscle cell. This problem arises from the fact that the membrane of the muscle cell envelops the motor neuron terminal with a convoluted process called the subsynaptic reticulum, obscuring the boundary between muscle and nerve. A first strategy entails taking thin optical sections through synaptic boutons to capture a cross section of the nerve terminal, and a second strategy involves visualizing epitope-tagged isoforms of particular proteins that have been transgenically expressed in either the nerve or the muscle.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Mexico 3 20%
Unknown 12 80%

Demographic breakdown

Readers by professional status Count As %
Researcher 6 40%
Professor 5 33%
Professor > Associate Professor 3 20%
Other 1 7%
Readers by discipline Count As %
Agricultural and Biological Sciences 5 33%
Psychology 2 13%
Chemistry 2 13%
Medicine and Dentistry 2 13%
Biochemistry, Genetics and Molecular Biology 1 7%
Other 3 20%