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Related Concept Videos

Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

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Confocal microscopy is an advanced microscopic technique. The prime advantage of the confocal microscope over other microscopy techniques is its ability to block the out-of-focus light from the illuminated samples using pinholes. It is widely used with fluorescence optics to obtain high-resolution, sharp contrast images. Unlike optical microscopes, confocal microscopes use a focused beam of light laser to scan the entire sample surface at different z-planes. These microscopes are, therefore,...
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Super-resolution Fluorescence Microscopy01:37

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Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
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Atomic Force Microscopy01:08

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Atomic force microscopy (AFM) is a type of scanning probe microscopy that can analyze topographic details of various specimens like ceramics, glass, polymers, and biological samples. AFM offers over 1000 times more resolution than the optical imaging system. Images generated from AFM are three-dimensional surface profiles, offering an advantage over the flat, two-dimensional images from other imaging techniques.
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Related Experiment Video

Updated: Nov 25, 2025

Open Source High Content Analysis Utilizing Automated Fluorescence Lifetime Imaging Microscopy
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New solution for fast axial scanning in fluorescence microscopy.

Weijian Zong1

  • 1Kavli Institute for Systems Neuroscience and Centre for Neural Computation, Norwegian University of Science and Technology, Trondheim, Norway. weijian.zong@ntnu.no.

Light, Science & Applications
|December 15, 2020
PubMed
Summary

Researchers developed a new 3D fluorescence imaging technique. This method uses a galvanometer scanner and a special mirror to achieve fast, subcellular imaging by converting lateral scanning into axial scanning.

Area of Science:

  • Microscopy
  • Biophotonics
  • Optical Imaging

Background:

  • Traditional 3D fluorescence microscopy often faces limitations in speed and resolution, particularly for subcellular imaging.

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  • Achieving rapid volumetric imaging at the subcellular level is crucial for understanding dynamic biological processes.