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

Single-cell analyses identify the ginseng embryonic protoderm as a native compartment for high-efficiency ginsenoside production.

Nature communications·2026
Same author

Physcomitrium LATERAL SUPPRESSOR genes promote formative cell divisions to produce germ cell lineages in both male and female gametangia.

The New phytologist·2024
Same author

Proteins and noncoding RNAs that promote homologous chromosome recognition and pairing in fission yeast meiosis undergo condensate formation in vitro.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology·2024
Same author

Transport-of-intensity phase imaging using commercially available confocal microscope.

Journal of biomedical optics·2024
Same author

Fission yeast Wee1 is required for stable kinetochore-microtubule attachment.

Open biology·2024
Same author

Phosphoregulation of DSB-1 mediates control of meiotic double-strand break activity.

eLife·2022
Same journal

Ultrahigh-speed micromachining of sapphire by enhancing laser absorption.

Communications engineering·2026
Same journal

Industry-Academia Interface: Exploring the growth of Additive Manufacturing as an industry with Laura Del Río Fernández.

Communications engineering·2026
Same journal

Operating smart grids by customizing large model agents.

Communications engineering·2026
Same journal

Photovoltaics for space applications.

Communications engineering·2026
Same journal

EdgeVolution: democratizing multi-objective neural architecture search and end-to-end deployment on microcontrollers.

Communications engineering·2026
Same journal

Ghost noise in single-fiber bidirectional transmission links and its suppression approaches.

Communications engineering·2026
See all related articles

Related Experiment Video

Updated: Mar 11, 2026

Time Multiplexing Super Resolving Technique for Imaging from a Moving Platform
06:25

Time Multiplexing Super Resolving Technique for Imaging from a Moving Platform

Published on: February 12, 2014

8.9K

Phase-based computational adaptive optics enables artifact-free super-resolution microscopy.

Atsushi Matsuda1, Carlos Mario Rodriguez-Reza2, Yosuke Tamada3,4,5

  • 1Advanced ICT Research Institute, National Institute of Information and Communications Technology, Kobe, Japan. a.matsuda@nict.go.jp.

Communications Engineering
|March 10, 2026
PubMed
Summary
This summary is machine-generated.

We developed ∅CAO, a computational adaptive optics method for clearer 3D microscopy. This technique corrects aberrations without special hardware, making high-resolution biological imaging more accessible.

More Related Videos

Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers
10:07

Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers

Published on: April 9, 2014

10.7K
Confocal and Super-Resolution Imaging of Polarized Intracellular Trafficking and Secretion of Basement Membrane Proteins During Drosophila Oogenesis
10:41

Confocal and Super-Resolution Imaging of Polarized Intracellular Trafficking and Secretion of Basement Membrane Proteins During Drosophila Oogenesis

Published on: May 19, 2022

2.6K

Related Experiment Videos

Last Updated: Mar 11, 2026

Time Multiplexing Super Resolving Technique for Imaging from a Moving Platform
06:25

Time Multiplexing Super Resolving Technique for Imaging from a Moving Platform

Published on: February 12, 2014

8.9K
Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers
10:07

Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers

Published on: April 9, 2014

10.7K
Confocal and Super-Resolution Imaging of Polarized Intracellular Trafficking and Secretion of Basement Membrane Proteins During Drosophila Oogenesis
10:41

Confocal and Super-Resolution Imaging of Polarized Intracellular Trafficking and Secretion of Basement Membrane Proteins During Drosophila Oogenesis

Published on: May 19, 2022

2.6K

Area of Science:

  • Biomedical Engineering
  • Optical Microscopy
  • Computational Imaging

Background:

  • Adaptive optics (AO) enhances microscopy resolution and signal-to-noise ratio.
  • Current AO methods require complex hardware and can cause phototoxicity, limiting widespread use.
  • There is a need for accessible AO solutions in biological imaging.

Purpose of the Study:

  • To introduce ∅CAO, a computational phase-based AO technique.
  • To enable aberration correction in 3D fluorescence microscopy without specialized optics or training data.
  • To improve the accessibility and scalability of AO for life sciences.

Main Methods:

  • Utilized phase transfer functions in the frequency domain for aberration correction.
  • Developed a computational approach for post-acquisition image correction.
  • Applied the technique to diverse imaging modalities like wide-field and structured illumination microscopy.

Main Results:

  • Achieved substantial improvements in image fidelity and resolution.
  • Demonstrated robust performance under noisy imaging conditions.
  • Successfully corrected optical aberrations in biological specimens, including C. elegans and plant tissues.

Conclusions:

  • ∅CAO provides a scalable and accessible solution for high-resolution biological imaging.
  • The computational, phase-based approach overcomes limitations of traditional AO hardware.
  • Facilitates broader adoption of advanced AO techniques in life science research.