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High-Throughput Screening Assays in Toxicology

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Cover of 'High-Throughput Screening Assays in Toxicology'

Table of Contents

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    Book Overview
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    Chapter 1 Monitoring Ligand-Activated Protein–Protein Interactions Using Bioluminescent Resonance Energy Transfer (BRET) Assay
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    Chapter 2 Mitochondrial Membrane Potential Assay
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    Chapter 3 High-Throughput Screening Assays in Toxicology
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    Chapter 4 Quantitative High-Throughput Luciferase Screening in Identifying CAR Modulators
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    Chapter 5 Transactivation and Coactivator Recruitment Assays for Measuring Farnesoid X Receptor Activity
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    Chapter 6 Cell-Based Assay for Identifying the Modulators of Antioxidant Response Element Signaling Pathway
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    Chapter 7 Study Liver Cytochrome P450 3A4 Inhibition and Hepatotoxicity Using DMSO-Differentiated HuH-7 Cells
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    Chapter 8 Determination of Histone H2AX Phosphorylation in DT40 Cells
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    Chapter 9 High-Throughput and High-Content Micronucleus Assay in CHO-K1 Cells
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    Chapter 10 High-Throughput Screening Assays in Toxicology
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    Chapter 11 High-Throughput Screening Assays in Toxicology
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    Chapter 12 A Quantitative High-Throughput Screening Data Analysis Pipeline for Activity Profiling
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    Chapter 13 Correction of Microplate Data from High-Throughput Screening
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    Chapter 14 CurveP Method for Rendering High-Throughput Screening Dose-Response Data into Digital Fingerprints
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    Chapter 15 Accounting Artifacts in High-Throughput Toxicity Assays
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    Chapter 16 Accessing the High-Throughput Screening Data Landscape
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    Chapter 17 Curating and Preparing High-Throughput Screening Data for Quantitative Structure-Activity Relationship Modeling
Attention for Chapter 8: Determination of Histone H2AX Phosphorylation in DT40 Cells
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Chapter title
Determination of Histone H2AX Phosphorylation in DT40 Cells
Chapter number 8
Book title
High-Throughput Screening Assays in Toxicology
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-6346-1_8
Pubmed ID
Book ISBNs
978-1-4939-6344-7, 978-1-4939-6346-1
Authors

Kana Nishihara, Sampada A. Shahane, Menghang Xia, Nishihara, Kana, Shahane, Sampada A., Xia, Menghang

Abstract

Visualization of DNA damage response protein recruitment to DNA damage sites enables measurement of the DNA damage. DNA double-strand breaks (DSBs) and blocked replication forks induce the phosphorylation of H2AX at serine 139 (γH2AX), and accumulate γH2AX which can then be detected as foci. The detection of γH2AX foci by immunostaining with antibodies that recognize γH2AX is an indicator of DSBs presence. This chapter describes the measurement of γH2AX immunostaining using a high-content imaging platform in chicken DT40 B-lymphocyte cell lines.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 4 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 4 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 1 25%
Researcher 1 25%
Other 1 25%
Unknown 1 25%
Readers by discipline Count As %
Pharmacology, Toxicology and Pharmaceutical Science 1 25%
Chemistry 1 25%
Medicine and Dentistry 1 25%
Unknown 1 25%