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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 6: Quantitative Fluorescence Measurements with Multicolor Flow Cytometry
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Chapter title
Quantitative Fluorescence Measurements with Multicolor Flow Cytometry
Chapter number 6
Book title
Flow Cytometry Protocols
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7346-0_6
Pubmed ID
Book ISBNs
978-1-4939-7344-6, 978-1-4939-7346-0
Authors

Lili Wang, Adolfas K. Gaigalas, James Wood

Abstract

Multicolor flow cytometer assays are routinely used in clinical laboratories for immunophenotyping, monitoring disease and treatment, and determining prognostic factors. However, existing methods for quantitative measurements have not yet produced satisfactory results independent of flow cytometers used. This chapter details a procedure for quantifying surface and intracellular protein biomarkers by calibrating the output of a multicolor flow cytometer in units of antibodies bound per cell (ABC). The procedure includes the following critical steps: (a) quality control (QC) and performance characterization of the multicolor flow cytometer, (b) fluorescence calibration using hard dyed microspheres assigned with fluorescence intensity values in equivalent number of reference fluorophores (ERF), (c) compensation for correction of fluorescence spillover, and (d) application of a biological reference standard for translating the ERF scale to the ABC scale. The chapter also points out current efforts for implementing quantification of biomarkers in a manner which is independent of instrument platforms and reagent differences.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 19 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 5%
Unknown 18 95%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 26%
Other 2 11%
Student > Ph. D. Student 1 5%
Student > Bachelor 1 5%
Student > Master 1 5%
Other 1 5%
Unknown 8 42%
Readers by discipline Count As %
Medicine and Dentistry 4 21%
Biochemistry, Genetics and Molecular Biology 3 16%
Pharmacology, Toxicology and Pharmaceutical Science 1 5%
Computer Science 1 5%
Agricultural and Biological Sciences 1 5%
Other 2 11%
Unknown 7 37%