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Flow Cytometry Protocols

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Cover of 'Flow Cytometry Protocols'

Table of Contents

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    Book Overview
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    Chapter 1 Flow Cytometry: The Glass Is Half Full
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    Chapter 2 High-Dimensional Modeling for Cytometry: Building Rock Solid Models Using GemStone™ and Verity Cen-se’™ High-Definition t-SNE Mapping
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    Chapter 3 Mass Cytometry Assays for Antigen-Specific T Cells Using CyTOF
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    Chapter 4 RNA Flow Cytometry Using the Branched DNA Technique
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    Chapter 5 Analysis of Individual Extracellular Vesicles by Flow Cytometry
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    Chapter 6 Quantitative Fluorescence Measurements with Multicolor Flow Cytometry
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    Chapter 7 High Throughput Flow Cytometry for Cell Surface Profiling
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    Chapter 8 Multiparameter Conventional Flow Cytometry
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    Chapter 9 Multiparameter Intracellular Cytokine Staining
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    Chapter 10 Multiparametric Analysis of Apoptosis by Flow Cytometry
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    Chapter 11 Multiparameter Cell Cycle Analysis
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    Chapter 12 Monitoring Cell Proliferation by Dye Dilution: Considerations for Probe Selection
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    Chapter 13 Immunophenotypic Identification of Early Myeloerythroid Development
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    Chapter 14 Flow Cytometry Assays in Primary Immunodeficiency Diseases
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    Chapter 15 Real-Time Deformability Cytometry: Label-Free Functional Characterization of Cells
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    Chapter 16 Nuclear Cytometry: Analysis of the Patterns of DNA Synthesis and Transcription Using Flow Cytometry, Confocal Microscopy, and RNA Sequencing
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    Chapter 17 Flow Cytometric FRET Analysis of Protein Interactions
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    Chapter 18 Overview of Fluorescence Lifetime Measurements in Flow Cytometry
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    Chapter 19 Overview of Lasers for Flow Cytometry
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    Chapter 20 Flow Cytometry: The Glass Is Half Empty
Attention for Chapter 8: Multiparameter Conventional Flow Cytometry
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Chapter title
Multiparameter Conventional Flow Cytometry
Chapter number 8
Book title
Flow Cytometry Protocols
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7346-0_8
Pubmed ID
Book ISBNs
978-1-4939-7344-6, 978-1-4939-7346-0
Authors

Katherine M. McKinnon

Abstract

Multicolor flow cytometry is a useful technique when examining mixed populations of cells, such as blood and tissue cells in human and animal samples. The ability to use multiple fluorescent markers simultaneously allows for the identification of multiple cell types, as well as functional markers that further characterize each sample. The introduction of instruments capable of measuring 12-plus colors and new reagents has made this type of flow cytometry both popular and problematic. Adapting a typical staining panel from 4 to 6 color tubes to more than 12 colors is not simply a matter of "plug and play", but must be approached in a systematic manner to achieve a successful multi-parameter staining panel. This chapter will examine the considerations and methods needed to successfully perform multicolor flow cytometry.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 35 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 35 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 6 17%
Researcher 5 14%
Student > Ph. D. Student 5 14%
Student > Master 4 11%
Student > Doctoral Student 2 6%
Other 1 3%
Unknown 12 34%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 8 23%
Immunology and Microbiology 5 14%
Medicine and Dentistry 3 9%
Agricultural and Biological Sciences 3 9%
Pharmacology, Toxicology and Pharmaceutical Science 1 3%
Other 3 9%
Unknown 12 34%