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Cell Viability Assays

Overview of attention for book
Cover of 'Cell Viability Assays'

Table of Contents

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    Book Overview
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    Chapter 1 Basic Colorimetric Proliferation Assays: MTT, WST, and Resazurin
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    Chapter 2 Assaying Cellular Viability Using the Neutral Red Uptake Assay
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    Chapter 3 Assessment of Cell Viability with Single-, Dual-, and Multi-Staining Methods Using Image Cytometry
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    Chapter 4 High-Throughput Spheroid Screens Using Volume, Resazurin Reduction, and Acid Phosphatase Activity
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    Chapter 5 A Protocol for In Vitro High-Throughput Chemical Susceptibility Screening in Differentiating NT2 Stem Cells
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    Chapter 6 Ferroptosis and Cell Death Analysis by Flow Cytometry
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    Chapter 7 Assaying Mitochondrial Respiration as an Indicator of Cellular Metabolism and Fitness
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    Chapter 8 An ATP-Based Luciferase Viability Assay for Animal African Trypanosomes Using a 96-Well Plate
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    Chapter 9 SYBR® Green I-Based Fluorescence Assay to Assess Cell Viability of Malaria Parasites for Routine Use in Compound Screening
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    Chapter 10 Screening Applications to Test Cellular Fitness in Transwell® Models After Nanoparticle Treatment
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    Chapter 11 Assays for Analyzing the Role of Transport Proteins in the Uptake and the Vectorial Transport of Substances Affecting Cell Viability
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    Chapter 12 Metabolite Profiling of Mammalian Cell Culture Processes to Evaluate Cellular Viability
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    Chapter 13 Assaying Spontaneous Network Activity and Cellular Viability Using Multi-well Microelectrode Arrays
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    Chapter 14 Quantitative Ratiometric Ca2+ Imaging to Assess Cell Viability
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    Chapter 15 Functional Viability: Measurement of Synaptic Vesicle Pool Sizes
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    Chapter 16 Phenotyping Cellular Viability by Functional Analysis of Ion Channels: GlyR-Targeted Screening in NT2-N Cells
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    Chapter 17 Systematic Cell-Based Phenotyping of Missense Alleles
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    Chapter 18 Second Harmonic Generation Microscopy of Muscle Cell Morphology and Dynamics
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    Chapter 19 Assessment of Population and ECM Production Using Multiphoton Microscopy as an Indicator of Cell Viability
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    Chapter 20 Average Rheological Quantities of Cells in Monolayers
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    Chapter 21 Measurement of Cellular Behavior by Electrochemical Impedance Sensing
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    Chapter 22 Nano-QSAR Model for Predicting Cell Viability of Human Embryonic Kidney Cells
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    Chapter 23 Erratum to: Functional Viability: Measurement of Synaptic Vesicle Pool Sizes
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    Chapter 24 Erratum to: Phenotyping Cellular Viability by Functional Analysis of Ion Channels: GlyR-Targeted Screening in NT2-N Cells
Attention for Chapter 9: SYBR® Green I-Based Fluorescence Assay to Assess Cell Viability of Malaria Parasites for Routine Use in Compound Screening
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Chapter title
SYBR® Green I-Based Fluorescence Assay to Assess Cell Viability of Malaria Parasites for Routine Use in Compound Screening
Chapter number 9
Book title
Cell Viability Assays
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6960-9_9
Pubmed ID
Book ISBNs
978-1-4939-6959-3, 978-1-4939-6960-9, 978-1-4939-6959-3, 978-1-4939-6960-9
Authors

Maria Leidenberger, Cornelia Voigtländer, Nina Simon, Barbara Kappes

Editors

Daniel F. Gilbert, Oliver Friedrich

Abstract

Owing to its fast and reliable assessment of parasite growth, the SYBR(®) Green I-based fluorescence assay is widely used to monitor drug susceptibility of malaria parasites. Its particular advantages are that it is a simple, one-step procedure and very cost-effective making it especially suited for high through put screening of newly developed drugs and drug combinations. Here we describe a SYBR(®) Green I-based fluorescence assay protocol to be used for routine screening of compounds and extracts in a research laboratory environment. A variation of the standard protocol is also provided allowing to address stage-specific effects of fast-acting drugs.

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X Demographics

The data shown below were collected from the profiles of 2 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 27 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 27 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 9 33%
Student > Master 3 11%
Student > Postgraduate 2 7%
Student > Bachelor 1 4%
Lecturer 1 4%
Other 2 7%
Unknown 9 33%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 7 26%
Pharmacology, Toxicology and Pharmaceutical Science 3 11%
Agricultural and Biological Sciences 2 7%
Chemistry 2 7%
Immunology and Microbiology 1 4%
Other 1 4%
Unknown 11 41%
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 05 May 2017.
All research outputs
#18,546,002
of 22,968,808 outputs
Outputs from Methods in molecular biology
#7,942
of 13,142 outputs
Outputs of similar age
#311,285
of 421,088 outputs
Outputs of similar age from Methods in molecular biology
#693
of 1,074 outputs
Altmetric has tracked 22,968,808 research outputs across all sources so far. This one is in the 11th percentile – i.e., 11% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,142 research outputs from this source. They receive a mean Attention Score of 3.4. This one is in the 24th percentile – i.e., 24% of its peers scored the same or lower than it.
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We're also able to compare this research output to 1,074 others from the same source and published within six weeks on either side of this one. This one is in the 21st percentile – i.e., 21% of its contemporaries scored the same or lower than it.