Time Course Microscopy

Time course microscopy is a technique for imaging the same biological specimen at defined intervals to measure how its structure or behavior changes over time. By repeatedly capturing bright-field or fluorescence images under controlled conditions, researchers can assemble a time series that reveals dynamic processes such as cell division, migration, differentiation, and intracellular transport. In biology, this approach links cellular events to their timing and sequence, helping distinguish transient responses from sustained changes. Quantitative analysis of image series can also measure growth rates, movement, and population behavior, supporting studies of development, disease mechanisms, drug effects, and tissue organization.

Time Course Microscopy - Related Videos

Research

JoVE Journal - Biology
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Time-lapse Microscopy of Early Embryogenesis in Caenorhabditis elegans

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Cited by 8 •

2011

This article describes a technique for the visualization of the early events of embryogenesis in the nematode Caenorhabditis elegans.

Research

JoVE EoE - Bacterial Growth and Techniques

Microfluidic Time-Lapse Microscopy to Study Antibiotic Persistence in Bacteria

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2025

Source: Oms, T., et al. Population and Single-Cell Analysis of Antibiotic Persistence in Escherichia coli. J. Vis. Exp. (2023)This video presents a protocol for monitoring individual bacterial cells expressing a fluorescently labeled DNA-binding protein within a microfluidic system. It illustrates how antibiotics inhibit most cells, while a subpopulation of persister cells survives the treatment and regrows following antibiotic removal.

Quantitative Analysis of Random Migration of Cells Using Time-lapse Video Microscopy

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Cited by 26 •

2012

This method allows monitoring of cells in real time and quantitative measurements of different cell migration parameters such as speed, displacement, and velocity. Unlike the traditional methods, this real time approach is not based on endpoint quantitative migration measurements; instead it allows monitoring and calculating different parameters continuously.

Studying Interactions of Staphylococcus aureus with Neutrophils by Flow Cytometry and Time Lapse Microscopy

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Cited by 25 •

2013

We present methods to study the effect of PSMs and other toxins secreted by Staphylococcus aureus on neutrophils using flow cytometry and fluorescence microscopy.

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