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Related Concept Videos

Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

7.0K
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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Confocal Fluorescence Microscopy01:16

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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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Related Experiment Video

Updated: Jul 9, 2025

Deep-Tissue Three-Photon Fluorescence Microscopy in Intact Mouse and Zebrafish Brain
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A Large Field-of-view, Single-cell-resolution Two- and Three-Photon Microscope for Deep Imaging.

Aaron T Mok1,2, Tianyu Wang1, Shitong Zhao1

  • 1School of Applied Engineering Physics, Cornell University, NY, USA.

Biorxiv : the Preprint Server for Biology
|November 28, 2023
PubMed
Summary
This summary is machine-generated.

Researchers developed new three-photon microscopy techniques to overcome field-of-view limitations for deep brain imaging. This allows unprecedented large-scale, high-speed neuronal activity mapping in scattering tissues.

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Area of Science:

  • Neuroscience
  • Biomedical Engineering
  • Optical Imaging

Background:

  • In vivo imaging of neural networks is crucial for understanding brain function.
  • Multiphoton microscopy advances speed, field of view, and depth but faces limitations in scattering tissues.
  • Field of view in deep-tissue imaging decreases exponentially with depth due to thermal damage concerns.

Conclusions:

  • The developed innovations overcome limitations in deep-tissue multiphoton imaging.
  • These techniques facilitate large-field-of-view, system-level neural circuit research.
  • The methods are adaptable to existing multiphoton microscopes.