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

Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

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,...
Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

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 developed.
Phase Contrast and Differential Interference Contrast Microscopy01:26

Phase Contrast and Differential Interference Contrast Microscopy

Phase-Contrast Microscopes
In-phase-contrast microscopes, interference between light directly passing through a cell and light refracted by cellular components is used to create high-contrast, high-resolution images without staining. It is the oldest and simplest type of microscope that creates an image by altering the wavelengths of light rays passing through the specimen. Altered wavelength paths are created using an annular stop in the condenser. The annular stop produces a hollow cone of...

You might also read

Related Articles

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

Sort by
Same author

Effects of aerobic running vs. reading rest after fear extinction on recall: Decreased prefrontal cortex activity to distinguish threat and safety cues.

NeuroImage·2025
Same author

Accidental discharge of brodifacoum baits into a freshwater lake: a case study.

Bulletin of environmental contamination and toxicology·2011
Same author

Interface for coupling capillary electrophoresis to inductively coupled plasma and on-column concentration technique.

Analytical chemistry·2011
Same author

The eugenist.

The Eugenics review·2011
Same author

Taqman real-time quantitative PCR for identification of western flower thrip (Frankliniella occidentalis) for plant quarantine.

Biology letters·2010
Same author

Clinical characteristics and outcomes of diabetic patients with Staphylococcus aureus bacteremia and endocarditis.

European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology·2009

Related Experiment Video

Updated: May 19, 2026

Video-rate Scanning Confocal Microscopy and Microendoscopy
14:10

Video-rate Scanning Confocal Microscopy and Microendoscopy

Published on: October 20, 2011

A line scanning confocal fluorescent microscope using a CMOS rolling shutter as an adjustable aperture.

E Mei1, P A Fomitchov, R Graves

  • 1GE Healthcare, Life Sciences Division, Piscataway, NJ 08854, USA. erwen.mei@ge.com

Journal of Microscopy
|August 22, 2012
PubMed
Summary

This study introduces a novel line scanning confocal microscope using a software-controlled rolling shutter instead of a physical aperture. This innovation allows for real-time, adjustable confocal resolution for improved imaging in microscopy applications.

More Related Videos

Near Simultaneous Laser Scanning Confocal and Atomic Force Microscopy (Conpokal) on Live Cells
09:20

Near Simultaneous Laser Scanning Confocal and Atomic Force Microscopy (Conpokal) on Live Cells

Published on: August 11, 2020

Single Molecule Fluorescence Microscopy on Planar Supported Bilayers
20:00

Single Molecule Fluorescence Microscopy on Planar Supported Bilayers

Published on: October 31, 2015

Related Experiment Videos

Last Updated: May 19, 2026

Video-rate Scanning Confocal Microscopy and Microendoscopy
14:10

Video-rate Scanning Confocal Microscopy and Microendoscopy

Published on: October 20, 2011

Near Simultaneous Laser Scanning Confocal and Atomic Force Microscopy (Conpokal) on Live Cells
09:20

Near Simultaneous Laser Scanning Confocal and Atomic Force Microscopy (Conpokal) on Live Cells

Published on: August 11, 2020

Single Molecule Fluorescence Microscopy on Planar Supported Bilayers
20:00

Single Molecule Fluorescence Microscopy on Planar Supported Bilayers

Published on: October 31, 2015

Area of Science:

  • Microscopy and Imaging Technologies
  • Optical Physics

Background:

  • Traditional confocal microscopy relies on physical aperture barriers, limiting confocality control.
  • The fixed nature of physical apertures restricts real-time adjustments to imaging parameters.

Purpose of the Study:

  • To present a new line scanning confocal microscope design that replaces physical apertures with a software-controllable rolling shutter.
  • To demonstrate adjustable and independent confocal resolution per fluorescence channel.

Main Methods:

  • Implementation of a rolling shutter on a CMOS camera synchronized with laser line scanning.
  • Synchronization of rolling shutter width with laser scanning for image acquisition.
  • Real-time adjustment of confocal resolution by modifying rolling shutter width.

Main Results:

  • Successful elimination of the need for a physical aperture in confocal microscopy.
  • Demonstration of adjustable confocal resolution in real time.
  • Independent control of resolution for each fluorescence channel.

Conclusions:

  • The developed line scanning confocal microscope offers enhanced flexibility and control over confocality.
  • This technology enables adjustable resolution, improving imaging capabilities for various applications.
  • The system has been successfully implemented in the GE Healthcare IN Cell Analyzer 6000.