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Innate Antiviral Immunity

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Cover of 'Innate Antiviral Immunity'

Table of Contents

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    Book Overview
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    Chapter 1 The Application of Humanized Mouse Models for the Study of Human Exclusive Viruses
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    Chapter 2 Zebrafish as a Model for the Study of Host-Virus Interactions
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    Chapter 3 Northern Blot Detection of Virus-Derived Small Interfering RNAs in Caenorhabditis elegans Using Nonradioactive Oligo Probes
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    Chapter 4 Extraction and qPCR-Based Detection of miRNAs from Cultured PBMCs of Bubaline Origin
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    Chapter 5 Visualizing Virus-Derived dsRNA Using Antibody-Independent and -Dependent Methods
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    Chapter 6 RNA PAMPs as Molecular Tools for Evaluating RIG-I Function in Innate Immunity
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    Chapter 7 Methods to Visualize MAVS Subcellular Localization
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    Chapter 8 Purification of Cyclic GMP-AMP from Viruses and Measurement of Its Activity in Cell Culture
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    Chapter 9 cGAMP Quantification in Virus-Infected Human Monocyte-Derived Cells by HPLC-Coupled Tandem Mass Spectrometry
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    Chapter 10 Methods of Assessing STING Activation and Trafficking
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    Chapter 11 Genome-Wide CRISPR/Cas9 Screening for High-Throughput Functional Genomics in Human Cells
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    Chapter 12 High-Throughput Screening for Identification of Novel Innate Immune Activators
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    Chapter 13 Chromosome Conformation Capture for Research on Innate Antiviral Immunity
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    Chapter 14 Discovery of Variants Underlying Host Susceptibility to Virus Infection Using Whole-Exome Sequencing
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    Chapter 15 Isolation, Purification, and Culture of Primary Murine Sensory Neurons
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    Chapter 16 Isolation of Group 2 Innate Lymphoid Cells from Mouse Lungs
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    Chapter 17 Epidemiological Methods
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    Chapter 18 Erratum to: Purification of Cyclic GMP-AMP from Viruses and Measurement of Its Activity in Cell Culture
Attention for Chapter 5: Visualizing Virus-Derived dsRNA Using Antibody-Independent and -Dependent Methods
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Chapter title
Visualizing Virus-Derived dsRNA Using Antibody-Independent and -Dependent Methods
Chapter number 5
Book title
Innate Antiviral Immunity
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-7237-1_5
Pubmed ID
Book ISBNs
978-1-4939-7236-4, 978-1-4939-7237-1
Authors

Sarah J. Poynter, Stephanie J. DeWitte-Orr, Poynter, Sarah J., DeWitte-Orr, Stephanie J.

Abstract

Long double-stranded (ds) RNA molecules are produced as a byproduct of viral replication. Studying virus-derived dsRNA is important for understanding virus replication, understanding host responses to virus infections, and as a diagnostic tool for virus presence and replication. Here, we describe four different techniques for visualizing dsRNA; two antibody-dependent methods (immunoblotting and immunocytochemistry), as well as two antibody-independent methods (differential digestion and acridine orange staining). The benefits and disadvantages of each technique are also discussed.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 7 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 7 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 2 29%
Other 1 14%
Student > Ph. D. Student 1 14%
Unknown 3 43%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 1 14%
Nursing and Health Professions 1 14%
Immunology and Microbiology 1 14%
Medicine and Dentistry 1 14%
Engineering 1 14%
Other 0 0%
Unknown 2 29%