Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Related Concept Videos

You might also read

Related Articles

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

Sort by

Same author

Germline cancer susceptibility gene variants, somatic second hits, and survival outcomes in patients with resected pancreatic cancer.

Genetics in medicine : official journal of the American College of Medical Genetics·2018

Same author

[Expression,Purification,Structure Determination and Immunogenicity Assay of Hepatitis E Virus Capsid Protein p495 Derived from Baculovirus-based Insect Cell].

Bing du xue bao = Chinese journal of virology·2018

Same author

Mesoporous TiO<sub>2</sub> with WO<sub>3</sub> functioning as dopant and light-sensitizer: A highly efficient photocatalyst for degradation of organic compound.

Journal of hazardous materials·2018

Same author

Jia-Jian-Di-Huang-Yin-Zi decoction exerts neuroprotective effects on dopaminergic neurons and their microenvironment.

Scientific reports·2018

Same author

Reasons for Proficiency Testing Failures in Routine Chemistry Analysis in China.

Laboratory medicine·2018

Same author

Di-metal-doped sulfur resisting perovskite catalysts for highly efficient H<sub>2</sub>-SCR of NO.

Environmental science and pollution research international·2018

Search research articles

Related Experiment Video

Updated: Sep 25, 2025

Imaging C. elegans Embryos using an Epifluorescent Microscope and Open Source Software

Imaging C. elegans Embryos using an Epifluorescent Microscope and Open Source Software

Published on: March 24, 2011

Live imaging of postembryonic developmental processes in C. elegans.

Tingting Li^1,2,3, Xinjian Wang¹, Zhigang Feng¹

¹School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.

|May 2, 2022

Summary

This study presents a live imaging protocol for analyzing dynamic cellular processes like neuronal migration and dendritic growth in Caenorhabditis elegans (C. elegans). The method offers detailed insights into cellular dynamics during postembryonic development.

Keywords:

Cell Biology Developmental biology Microscopy Model Organisms

More Related Videos

High-Resolution C. elegans Imaging Across All Larval Stages

High-Resolution C. elegans Imaging Across All Larval Stages

Published on: May 23, 2025

A Semi-high-throughput Imaging Method and Data Visualization Toolkit to Analyze C. elegans Embryonic Development

A Semi-high-throughput Imaging Method and Data Visualization Toolkit to Analyze C. elegans Embryonic Development

Published on: October 29, 2019

Related Experiment Videos

Last Updated: Sep 25, 2025

Imaging C. elegans Embryos using an Epifluorescent Microscope and Open Source Software

Imaging C. elegans Embryos using an Epifluorescent Microscope and Open Source Software

Published on: March 24, 2011

High-Resolution C. elegans Imaging Across All Larval Stages

High-Resolution C. elegans Imaging Across All Larval Stages

Published on: May 23, 2025

A Semi-high-throughput Imaging Method and Data Visualization Toolkit to Analyze C. elegans Embryonic Development

A Semi-high-throughput Imaging Method and Data Visualization Toolkit to Analyze C. elegans Embryonic Development

Published on: October 29, 2019

Area of Science:

Developmental Biology
Neuroscience
Microscopy

Background:

Live imaging is crucial for observing dynamic biological processes.
Understanding cellular dynamics in development requires advanced imaging techniques.

Purpose of the Study:

To describe a protocol for time-lapse microscopy analysis.
To provide a method for studying neuronal patterning, migration, and dendritic growth.

Main Methods:

Utilizing time-lapse microscopy.
Applying the protocol to Caenorhabditis elegans (C. elegans) postembryonic development.

Main Results:

The protocol yields detailed information on cellular dynamics.
Demonstrates application in analyzing neuronal migration and dendritic growth.

Conclusions:

The described protocol is valuable for studying postembryonic development in C. elegans.
Facilitates detailed understanding of neuronal development and cellular dynamics.