Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Flow Cytometry01:23

Flow Cytometry

The development of flow cytometry techniques began in 1934 with initial attempts by Andrew Moldavan, a bacteriologist who counted the cells in a flowing capillary system. Moldavan pumped cells through a capillary tube focused under a microscope for visualization. The invention of photometry allowed the measurement of differentially-stained cells, and Louis Kamentsky developed the first multiparameter flow cytometer in 1965 to identify and count the cancer cells in cervical tissue specimens.
In...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Analysing outbreak signals, 2013-2024: The amsterdam UMC centre for Tropical Medicine and Travel Medicine Epi Alert programme - an observational study.

New microbes and new infections·2026
Same author

The impact of state-of-the-art pharmacotherapy for malaria in infants: a breakthrough?

Expert opinion on pharmacotherapy·2026
Same author

Single-cell transcriptomics of bronchoalveolar lavage reveals divergent macrophage subpopulations and trajectories in interstitial lung disease.

PloS one·2026
Same author

Alveolar Lipid-Macrophage Networks at the Intersection of Pulmonary Fibrosis.

Cells·2026
Same author

Malaria Prevention: Progress to Date.

Drugs·2026
Same author

Modifications of the Helmintex Method: Integration of Treatments With Tween 20, Cellulase, Percoll and Auramine-O Staining for Detection of Schistosoma mansoni Eggs.

Tropical medicine & international health : TM & IH·2026
Same journal

Detection and Sorting of Extracellular Vesicles and Viruses Using nanoFACS.

Current protocols in cytometry·2020
Same journal

Live Imaging of the Lung.

Current protocols in cytometry·2020
Same journal

Small Particle Fluorescence and Light Scatter Calibration Using FCM<sub>PASS</sub> Software.

Current protocols in cytometry·2020
Same journal

Optimized Stochastic Optical Reconstruction Microscopy for Imaging Chromatin Structure in Pathological Tissue.

Current protocols in cytometry·2020
Same journal

Flow Cytometric Quantification of Granulocytic Alkaline Phosphatase Activity in Unlysed Whole Blood.

Current protocols in cytometry·2020
Same journal

Practical Guidelines for Collection, Manipulation and Inactivation of SARS-CoV-2 and COVID-19 Clinical Specimens.

Current protocols in cytometry·2020
See all related articles

Related Experiment Video

Updated: May 9, 2026

In Vivo Assessment of Rodent Plasmodium Parasitemia and Merozoite Invasion by Flow Cytometry
07:16

In Vivo Assessment of Rodent Plasmodium Parasitemia and Merozoite Invasion by Flow Cytometry

Published on: April 5, 2015

Cytometry in malaria--a practical replacement for microscopy?

Howard M Shapiro1, Simon H Apte2, Grace M Chojnowski2

  • 1The Center for Microbial Cytometry, West Newton, Massachusetts.

Current Protocols in Cytometry
|July 10, 2013
PubMed
Summary
This summary is machine-generated.

Accurate malaria diagnosis is crucial as microscopy methods are limited. New imaging cytometers offer a more precise and objective diagnostic tool for detecting Plasmodium parasites, improving malaria detection rates.

More Related Videos

In Vitro Assay of Plasmodium-Infected Red Blood Cell Killing by Cytotoxic Lymphocytes
08:20

In Vitro Assay of Plasmodium-Infected Red Blood Cell Killing by Cytotoxic Lymphocytes

Published on: August 17, 2022

Detection and Quantification of Plasmodium falciparum in Aqueous Red Blood Cells by Attenuated Total Reflection Infrared Spectroscopy and Multivariate Data Analysis
10:50

Detection and Quantification of Plasmodium falciparum in Aqueous Red Blood Cells by Attenuated Total Reflection Infrared Spectroscopy and Multivariate Data Analysis

Published on: November 2, 2018

Related Experiment Videos

Last Updated: May 9, 2026

In Vivo Assessment of Rodent Plasmodium Parasitemia and Merozoite Invasion by Flow Cytometry
07:16

In Vivo Assessment of Rodent Plasmodium Parasitemia and Merozoite Invasion by Flow Cytometry

Published on: April 5, 2015

In Vitro Assay of Plasmodium-Infected Red Blood Cell Killing by Cytotoxic Lymphocytes
08:20

In Vitro Assay of Plasmodium-Infected Red Blood Cell Killing by Cytotoxic Lymphocytes

Published on: August 17, 2022

Detection and Quantification of Plasmodium falciparum in Aqueous Red Blood Cells by Attenuated Total Reflection Infrared Spectroscopy and Multivariate Data Analysis
10:50

Detection and Quantification of Plasmodium falciparum in Aqueous Red Blood Cells by Attenuated Total Reflection Infrared Spectroscopy and Multivariate Data Analysis

Published on: November 2, 2018

Area of Science:

  • Parasitology
  • Medical diagnostics
  • Biotechnology

Background:

  • Malaria, caused by Plasmodium parasites, results in approximately 800,000 deaths annually.
  • Current diagnostic methods, primarily microscopy, are subjective and struggle with low parasite densities.
  • Existing diagnostic tests often rely on microscopy for quality control, limiting their accuracy.

Purpose of the Study:

  • To evaluate the potential of quantitative flow cytometry measurements for malaria diagnosis.
  • To explore the application of these measurements in smaller, more accessible imaging cytometers.
  • To improve the accuracy and precision of malaria detection, especially in low-parasitemia cases.

Main Methods:

  • Quantitative flow cytometry was used to measure cellular constituents like DNA, RNA, and hemozoin in infected blood.
  • These measurements were assessed for their ability to identify Plasmodium species and developmental stages.
  • The feasibility of implementing these techniques in smaller, cost-effective imaging cytometers was investigated.

Main Results:

  • Flow cytometry provides objective and quantitative data on parasite load and characteristics.
  • Measurements of DNA, RNA, and hemozoin offer reliable identification of parasite species and stages.
  • Imaging cytometers show potential for accurate detection of low-density parasitemia, surpassing microscopy.

Conclusions:

  • Quantitative flow cytometry measurements represent a significant advancement over traditional microscopy for malaria diagnosis.
  • The development of smaller, cheaper imaging cytometers can make advanced malaria diagnostics more accessible.
  • This technology promises more accurate and precise malaria detection, aiding in disease control efforts.