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Related Experiment Video

Updated: Jul 15, 2026

Efficient and Rapid Isolation of Early-stage Embryos from Arabidopsis thaliana Seeds
08:05

Efficient and Rapid Isolation of Early-stage Embryos from Arabidopsis thaliana Seeds

Published on: June 7, 2013

A simple, robust and semi-automated parasite egg isolation protocol.

Ted H M Mes1, Maarten Eysker, Harm W Ploeger

  • 1Netherlands Institute of Ecology (NIOO-KNAW), Centre for Estuarine and Marine Ecology, POB 140, 4400AC, Yerseke, The Netherlands. t.mes@nioo.knaw.nl

Nature Protocols
|April 5, 2007
PubMed
Summary

This study introduces a novel protocol for large-scale nematode egg quantification from fecal samples. The method enhances efficiency for epidemiological and genetic studies of host-parasite interactions.

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Area of Science:

  • Veterinary Parasitology
  • Molecular Epidemiology
  • Host-Parasite Interactions

Background:

  • Accurate parasite quantification is crucial for understanding host-parasite dynamics.
  • Traditional methods like the McMaster technique are limited in sample size and standardization for large-scale studies.

Purpose of the Study:

  • To develop and describe a standardized protocol for high-throughput nematode egg quantification.
  • To facilitate large-scale epidemiological and genetic analyses of host-parasite interactions.

Main Methods:

  • A protocol utilizing low-density salt solution for flotation and centrifugation of nematode eggs.
  • Subsequent sucrose flotation and precipitation for clear egg preparations.
  • Analysis of up to 6g of feces per sample, with preparations suited for digital recording and automated counting.

Related Experiment Videos

Last Updated: Jul 15, 2026

Efficient and Rapid Isolation of Early-stage Embryos from Arabidopsis thaliana Seeds
08:05

Efficient and Rapid Isolation of Early-stage Embryos from Arabidopsis thaliana Seeds

Published on: June 7, 2013

Main Results:

  • The protocol yields clear, concentrated egg preparations in microtiter plates.
  • Processing time is approximately 40 minutes for 24 samples, from fecal suspension to digital recording.
  • Enables standardized processing of large sample volumes, overcoming limitations of traditional methods.

Conclusions:

  • The described protocol offers an efficient and scalable solution for parasite quantification.
  • It supports advanced analyses in host-parasite epidemiology and genetics through digital data acquisition.