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Neutrophil Methods and Protocols

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Cover of 'Neutrophil Methods and Protocols'

Table of Contents

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    Book Overview
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    Chapter 1 The Role of Neutrophils in the Immune System: An Overview
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    Chapter 2 Isolation of Human Neutrophils from Venous Blood
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    Chapter 3 Neutrophil Isolation from Nonhuman Species
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    Chapter 4 Collection of In Vivo Transmigrated Neutrophils from Human Skin
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    Chapter 5 Subcellular fractionation of human neutrophils and analysis of subcellular markers.
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    Chapter 6 Neutrophil Methods and Protocols
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    Chapter 7 Measurement of Phospholipid Metabolism in Intact Neutrophils
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    Chapter 8 Optical Methods for the Measurement and Manipulation of Cytosolic Calcium Signals in Neutrophils
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    Chapter 9 Analysis of Electrophysiological Properties and Responses of Neutrophils
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    Chapter 10 Assessment of Neutrophil Apoptosis
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    Chapter 11 Microinjection Methods for Neutrophils
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    Chapter 12 Generation of Functionally Mature Neutrophils from Induced Pluripotent Stem Cells
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    Chapter 13 Neutrophil Methods and Protocols
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    Chapter 14 Spinning disk confocal imaging of neutrophil migration in zebrafish.
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    Chapter 15 Detection of Bidirectional Signaling During Integrin Activation and Neutrophil Adhesion
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    Chapter 16 Immunofluorescence and confocal microscopy of neutrophils.
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    Chapter 17 Expression of genetically encoded fluorescent probes to monitor phospholipid dynamics in live neutrophils.
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    Chapter 18 Quantitative assessment of neutrophil phagocytosis using flow cytometry.
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    Chapter 19 Analysis of neutrophil bactericidal activity.
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    Chapter 20 Induction and quantification of neutrophil extracellular traps.
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    Chapter 21 Measurement of Respiratory Burst Products, Released or Retained, During Activation of Professional Phagocytes
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    Chapter 22 Cell-Free NADPH Oxidase Activation Assays: “In Vitro Veritas”
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    Chapter 23 Assessment of Priming of the Human Neutrophil Respiratory Burst
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    Chapter 24 Affinity purification and reconstitution of human phagocyte flavocytochrome B for detection of conformational dynamics in the membrane.
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    Chapter 25 Evaluation of p47phox Phosphorylation in Human Neutrophils Using Phospho-Specific Antibodies
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    Chapter 26 Genome-Scale Transcript Analyses with Human Neutrophils
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    Chapter 27 Fast and Accurate Quantitative Analysis of Cytokine Gene Expression in Human Neutrophils
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    Chapter 28 High-purity neutrophil isolation from human peripheral blood and saliva for transcriptome analysis.
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    Chapter 29 Detection of intact transcription factors in human neutrophils.
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    Chapter 30 Disorders of neutrophil function: an overview.
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    Chapter 31 Diagnostic Assays for Chronic Granulomatous Disease and Other Neutrophil Disorders
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    Chapter 32 Diagnostic Assays for Myeloperoxidase and Myeloperoxidase Deficiency
Attention for Chapter 18: Quantitative assessment of neutrophil phagocytosis using flow cytometry.
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Chapter title
Quantitative assessment of neutrophil phagocytosis using flow cytometry.
Chapter number 18
Book title
Neutrophil Methods and Protocols
Published in
Methods in molecular biology, February 2014
DOI 10.1007/978-1-62703-845-4_18
Pubmed ID
Book ISBNs
978-1-62703-844-7, 978-1-62703-845-4
Authors

Nordenfelt P, Pontus Nordenfelt, Nordenfelt, Pontus

Abstract

Neutrophils have an incredible ability to find and eradicate intruders such as bacteria and fungi. They do this largely through the process of phagocytosis, where the target is internalized into a phagosome, and eventually destroyed by the hostile phagosomal environment. It is important to study phagocytosis in order to understand how neutrophils interact with various pathogens and how they respond to different stimuli. Here, I describe a method to study neutrophil phagocytosis of bacteria using flow cytometry. The bacteria are fluorescently labeled before being introduced to neutrophils. After phagocytosis, both any remaining extracellular bacteria and neutrophils are labeled using one-step staining before three-color analysis. To assess phagocytosis, first the average time it takes for the neutrophils to internalize all bound bacteria is determined. Experiments are then performed using that time point while varying the bacteria-to-neutrophil ratio for full control of the analysis. Due to the ease with which multiple samples can be analyzed, and the quantitative nature of flow cytometry, this approach is both reproducible and sensitive.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 23 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 23 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 8 35%
Student > Master 3 13%
Student > Bachelor 3 13%
Researcher 2 9%
Other 1 4%
Other 2 9%
Unknown 4 17%
Readers by discipline Count As %
Agricultural and Biological Sciences 7 30%
Immunology and Microbiology 4 17%
Medicine and Dentistry 4 17%
Biochemistry, Genetics and Molecular Biology 2 9%
Veterinary Science and Veterinary Medicine 1 4%
Other 1 4%
Unknown 4 17%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 10 October 2014.
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#20,238,443
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Outputs from Methods in molecular biology
#9,865
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#268,328
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Outputs of similar age from Methods in molecular biology
#436
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