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High Throughput Screening

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Cover of 'High Throughput Screening'

Table of Contents

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    Book Overview
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    Chapter 1 Design and Implementation of High-Throughput Screening Assays
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    Chapter 2 Characterization of Inhibitor Binding Through Multiple Inhibitor Analysis: A Novel Local Fitting Method
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    Chapter 3 High Throughput Screening
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    Chapter 4 Structure-Based Virtual Screening of Commercially Available Compound Libraries
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    Chapter 5 AlphaScreen-Based Assays: Ultra-High-Throughput Screening for Small-Molecule Inhibitors of Challenging Enzymes and Protein-Protein Interactions
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    Chapter 6 Instrument Quality Control
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    Chapter 7 Application of Fluorescence Polarization in HTS Assays
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    Chapter 8 Time-Resolved Fluorescence Assays
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    Chapter 9 Protein Kinase Selectivity Profiling Using Microfluid Mobility Shift Assays
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    Chapter 10 Screening for Inhibitors of Kinase Autophosphorylation
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    Chapter 11 A Fluorescence-Based High-Throughput Screening Assay to Identify Growth Inhibitors of the Pathogenic Fungus Aspergillus fumigatus
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    Chapter 12 High Throughput Screening
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    Chapter 13 Identification of State-Dependent Blockers for Voltage-Gated Calcium Channels Using a FLIPR-Based Assay
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    Chapter 14 A Luciferase Reporter Gene System for High-Throughput Screening of γ -Globin Gene Activators
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    Chapter 15 A High-Throughput Flow Cytometry Assay for Identification of Inhibitors of 3′,5′-Cyclic Adenosine Monophosphate Efflux
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    Chapter 16 High-Throughput Cell Toxicity Assays
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    Chapter 17 BRET: NanoLuc-Based Bioluminescence Resonance Energy Transfer Platform to Monitor Protein-Protein Interactions in Live Cells
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    Chapter 18 Application of Imaging-Based Assays in Microplate Formats for High-Content Screening
Attention for Chapter 18: Application of Imaging-Based Assays in Microplate Formats for High-Content Screening
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Chapter title
Application of Imaging-Based Assays in Microplate Formats for High-Content Screening
Chapter number 18
Book title
High Throughput Screening
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3673-1_18
Pubmed ID
Book ISBNs
978-1-4939-3671-7, 978-1-4939-3673-1
Authors

Adam I. Fogel, Scott E. Martin, Samuel A. Hasson, Fogel, Adam I., Martin, Scott E., Hasson, Samuel A.

Abstract

The use of multiparametric microscopy-based screens with automated analysis has enabled the large-scale study of biological phenomena that are currently not measurable by any other method. Collectively referred to as high-content screening (HCS), or high-content analysis (HCA), these methods rely on an expanding array of imaging hardware and software automation. Coupled with an ever-growing amount of diverse chemical matter and functional genomic tools, HCS has helped open the door to a new frontier of understanding cell biology through phenotype-driven screening. With the ability to interrogate biology on a cell-by-cell basis in highly parallel microplate-based platforms, the utility of HCS continues to grow as advancements are made in acquisition speed, model system complexity, data management, and analysis systems. This chapter uses an example of screening for genetic factors regulating mitochondrial quality control to exemplify the practical considerations in developing and executing high-content campaigns.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 11 100%

Demographic breakdown

Readers by professional status Count As %
Other 1 9%
Student > Bachelor 1 9%
Student > Ph. D. Student 1 9%
Student > Master 1 9%
Researcher 1 9%
Other 1 9%
Unknown 5 45%
Readers by discipline Count As %
Engineering 2 18%
Biochemistry, Genetics and Molecular Biology 1 9%
Pharmacology, Toxicology and Pharmaceutical Science 1 9%
Agricultural and Biological Sciences 1 9%
Business, Management and Accounting 1 9%
Other 0 0%
Unknown 5 45%