Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

14.7K
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...
14.7K

You might also read

Related Articles

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

Sort by
Same author

Pan-Optical Shadow Imaging of Brain Microanatomy.

Methods in molecular biology (Clifton, N.J.)·2026
Same author

Structurally exclusive Teneurin complexes orchestrate divergent programs in early cortical development.

Nature communications·2026
Same author

Perinatal liver sympathetic innervation governs body size.

Communications biology·2026
Same author

Membrane-associated effluxosomes coordinate multi-metal resistance in Mycobacterium tuberculosis.

The EMBO journal·2026
Same author

Fast volumetric fluorescence lifetime imaging of multicellular systems using single-objective light-sheet microscopy.

Communications biology·2025
Same author

In-depth single molecule localization microscopy using adaptive optics and single objective light-sheet microscopy.

Nature communications·2025

Related Experiment Video

Updated: Mar 9, 2026

Super-Resolution Imaging to Study Co-Localization of Proteins and Synaptic Markers in Primary Neurons
14:02

Super-Resolution Imaging to Study Co-Localization of Proteins and Synaptic Markers in Primary Neurons

Published on: October 31, 2020

6.3K

Special Section Guest Editorial: Super-resolution microscopy of neural structure and function

U Valentin Nägerl1, Jean-Baptiste Sibarita1

  • 1University of Bordeaux-CNRS , Interdisciplinary Institute for Neuroscience , UMR5297, 33077 Bordeaux, France.

Neurophotonics
|January 3, 2017
PubMed
Summary

No abstract available in PubMed .

More Related Videos

A Scanning Electron Microscopy-Compatible Optical Imaging Method for Mesoscopic All-Cell Brain Mapping
09:40

A Scanning Electron Microscopy-Compatible Optical Imaging Method for Mesoscopic All-Cell Brain Mapping

Published on: February 20, 2026

106
Micron-scale Resolution Optical Tomography of Entire Mouse Brains with Confocal Light Sheet Microscopy
09:49

Micron-scale Resolution Optical Tomography of Entire Mouse Brains with Confocal Light Sheet Microscopy

Published on: October 8, 2013

17.2K

Related Experiment Videos

Last Updated: Mar 9, 2026

Super-Resolution Imaging to Study Co-Localization of Proteins and Synaptic Markers in Primary Neurons
14:02

Super-Resolution Imaging to Study Co-Localization of Proteins and Synaptic Markers in Primary Neurons

Published on: October 31, 2020

6.3K
A Scanning Electron Microscopy-Compatible Optical Imaging Method for Mesoscopic All-Cell Brain Mapping
09:40

A Scanning Electron Microscopy-Compatible Optical Imaging Method for Mesoscopic All-Cell Brain Mapping

Published on: February 20, 2026

106
Micron-scale Resolution Optical Tomography of Entire Mouse Brains with Confocal Light Sheet Microscopy
09:49

Micron-scale Resolution Optical Tomography of Entire Mouse Brains with Confocal Light Sheet Microscopy

Published on: October 8, 2013

17.2K