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Gap Junction Protocols

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Cover of 'Gap Junction Protocols'

Table of Contents

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    Book Overview
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    Chapter 1 Analysis of Liver Connexin Expression Using Reverse Transcription Quantitative Real-Time Polymerase Chain Reaction.
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    Chapter 2 Gap Junction Protocols
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    Chapter 3 Detection of Connexins in Liver Cells Using Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis and Immunoblot Analysis.
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    Chapter 4 Immunohisto- and Cytochemistry Analysis of Connexins.
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    Chapter 5 Small Interfering RNA-Mediated Connexin Gene Knockdown in Vascular Endothelial and Smooth Muscle Cells.
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    Chapter 6 Generation and Use of Trophoblast Stem Cells and Uterine Myocytes to Study the Role of Connexins for Pregnancy and Labor.
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    Chapter 7 Identification of Connexin43 Phosphorylation and S-Nitrosylation in Cultured Primary Vascular Cells.
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    Chapter 8 Preparation of Gap Junctions in Membrane Microdomains for Immunoprecipitation and Mass Spectrometry Interactome Analysis.
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    Chapter 9 Scrape Loading/Dye Transfer Assay.
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    Chapter 10 Microinjection Technique for Assessment of Gap Junction Function.
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    Chapter 11 Electroporation Loading and Dye Transfer: A Safe and Robust Method to Probe Gap Junctional Coupling.
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    Chapter 12 Using Fluorescence Recovery After Photobleaching to Study Gap Junctional Communication In Vitro.
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    Chapter 13 Tracking Dynamic Gap Junctional Coupling in Live Cells by Local Photoactivation and Fluorescence Imaging.
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    Chapter 14 Gap Junction Protocols
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    Chapter 15 Calcium Wave Propagation Triggered by Local Mechanical Stimulation as a Method for Studying Gap Junctions and Hemichannels.
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    Chapter 16 Establishment of the Dual Whole Cell Recording Patch Clamp Configuration for the Measurement of Gap Junction Conductance.
Attention for Chapter 12: Using Fluorescence Recovery After Photobleaching to Study Gap Junctional Communication In Vitro.
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Chapter title
Using Fluorescence Recovery After Photobleaching to Study Gap Junctional Communication In Vitro.
Chapter number 12
Book title
Gap Junction Protocols
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3664-9_12
Pubmed ID
Book ISBNs
978-1-4939-3662-5, 978-1-4939-3664-9
Authors

Maria Kuzma-Kuzniarska, Clarence Yapp, Philippa A. Hulley, Kuzma-Kuzniarska, Maria, Yapp, Clarence, Hulley, Philippa A.

Editors

Mathieu Vinken, Scott R. Johnstone

Abstract

Fluorescence recovery after photobleaching (FRAP) is a microscopy-based technique to study the movement of fluorescent molecules inside a cell. Although initially developed to investigate intracellular mobility, FRAP can be also used to measure intercellular dynamics. This chapter describes how to perform FRAP experiment to study gap junctional communication in living cells. The procedures described here can be carried out with a laser-scanning confocal microscope and any in vitro cultured cells known to communicate via gap junctions. In addition, the method can be easily adjusted to measure gap junction function in 3D cell cultures as well as ex vivo tissue.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 16 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 16 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 6 38%
Researcher 2 13%
Other 1 6%
Professor 1 6%
Student > Bachelor 1 6%
Other 2 13%
Unknown 3 19%
Readers by discipline Count As %
Agricultural and Biological Sciences 4 25%
Medicine and Dentistry 2 13%
Biochemistry, Genetics and Molecular Biology 2 13%
Pharmacology, Toxicology and Pharmaceutical Science 1 6%
Psychology 1 6%
Other 1 6%
Unknown 5 31%