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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 15: Real-Time Deformability Cytometry: Label-Free Functional Characterization of Cells
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Chapter title
Real-Time Deformability Cytometry: Label-Free Functional Characterization of Cells
Chapter number 15
Book title
Flow Cytometry Protocols
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7346-0_15
Pubmed ID
Book ISBNs
978-1-4939-7344-6, 978-1-4939-7346-0
Authors

Maik Herbig, Martin Kräter, Katarzyna Plak, Paul Müller, Jochen Guck, Oliver Otto

Abstract

Real-time deformability cytometry (RT-DC) is a microfluidic technique that allows to capture and evaluate morphology and rheology of up to 1000 cells/s in a constricted channel. The cells are deformed without mechanical contact by hydrodynamic forces and are quantified in real-time without the need of additional handling or staining procedures. Segmented pictures of the cells are stored and can be used for further analysis. RT-DC is sensitive to alterations of the cytoskeleton, which allows, e.g., to show differences in cell cycle phases, identify different subpopulations in whole blood and to study mechanical stiffening of cells entering a dormant state. The abundance of the obtainable parameters and the interpretation as mechanical readout is an analytical challenge that needs standardization. Here, we will provide guidelines for measuring and post-processing of RT-DC data.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 60 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 60 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 17 28%
Student > Master 8 13%
Researcher 7 12%
Student > Bachelor 3 5%
Student > Postgraduate 2 3%
Other 6 10%
Unknown 17 28%
Readers by discipline Count As %
Engineering 12 20%
Biochemistry, Genetics and Molecular Biology 8 13%
Physics and Astronomy 7 12%
Agricultural and Biological Sciences 4 7%
Medicine and Dentistry 3 5%
Other 4 7%
Unknown 22 37%