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,...
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...
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.
Three-Dimensional Microscopy in Microbiology01:28

Three-Dimensional Microscopy in Microbiology

Three-dimensional imaging techniques are essential in cell biology, allowing researchers to visualize intricate cellular structures with high resolution. Two prominent methods, Differential Interference Contrast Microscopy (DIC) and Confocal Scanning Laser Microscopy (CSLM), provide distinct advantages for imaging live and thick specimens, respectively.Differential Interference Contrast MicroscopyDIC microscopy enhances contrast in transparent, unstained samples by converting phase...

You might also read

Related Articles

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

Sort by
Same author

Bed occupancy and nosocomial infections in the intensive care unit: A retrospective observational study in a tertiary hospital.

The Southern African journal of critical care : the official journal of the Critical Care Society·2024
Same author

Minimally invasive cerebral revascularization in moyamoya disease in adult patients.

Neuro-Chirurgie·2022
Same author

Post-operative volumes following endoscopic surgery for non-functioning pituitary macroadenomas are predictive of further intervention, but not endocrine outcomes.

BMC endocrine disorders·2021
Same author

Treatment Preferences for Cardiac Procedures of Patients With Chronic Kidney Disease in Acute Coronary Syndrome: Design and Pilot Testing of a Discrete Choice Experiment.

Canadian journal of kidney health and disease·2021
Same author

Addressing the pitfalls when designing intervention studies to discover and validate biomarkers of habitual dietary intake.

Metabolomics : Official journal of the Metabolomic Society·2019
Same author

Purified Human Pancreatic Islets, CIT Culture Media with Lisofylline or Exenatide.

CellR4-- repair, replacement, regeneration, & reprogramming·2019

Related Experiment Video

Updated: Jun 10, 2026

Video-rate Scanning Confocal Microscopy and Microendoscopy
14:10

Video-rate Scanning Confocal Microscopy and Microendoscopy

Published on: October 20, 2011

Differential confocal scanning microscope with a two-mode optical fiber.

R Juskaitis, T Wilson

    Applied Optics
    |August 20, 2010
    PubMed
    Summary

    A new scanning microscope technique uses a two-mode optical fiber to create differential images. This method allows for the visualization of both amplitude and phase details in specimens.

    Area of Science:

    • Microscopy
    • Optical Imaging
    • Fiber Optics

    Background:

    • Differential imaging enhances contrast in microscopy.
    • Two-mode optical fibers offer unique light manipulation properties.

    Purpose of the Study:

    • To propose and demonstrate a novel technique for differential imaging using a two-mode optical fiber in scanning microscopy.
    • To achieve simultaneous acquisition of differential amplitude and phase images.

    Main Methods:

    • Utilizing a two-mode optical fiber within a scanning microscope setup.
    • Adjusting the differential phase delay between the fiber modes to control image acquisition.
    • Experimental validation of the proposed technique.

    Main Results:

    More Related Videos

    Conducting Multiple Imaging Modes with One Fluorescence Microscope
    08:32

    Conducting Multiple Imaging Modes with One Fluorescence Microscope

    Published on: October 28, 2018

    Super-Resolution Imaging and Shared Management: A Protocol for Confocal Microscopy with Multiplex Detection
    07:42

    Super-Resolution Imaging and Shared Management: A Protocol for Confocal Microscopy with Multiplex Detection

    Published on: February 24, 2026

    Related Experiment Videos

    Last Updated: Jun 10, 2026

    Video-rate Scanning Confocal Microscopy and Microendoscopy
    14:10

    Video-rate Scanning Confocal Microscopy and Microendoscopy

    Published on: October 20, 2011

    Conducting Multiple Imaging Modes with One Fluorescence Microscope
    08:32

    Conducting Multiple Imaging Modes with One Fluorescence Microscope

    Published on: October 28, 2018

    Super-Resolution Imaging and Shared Management: A Protocol for Confocal Microscopy with Multiplex Detection
    07:42

    Super-Resolution Imaging and Shared Management: A Protocol for Confocal Microscopy with Multiplex Detection

    Published on: February 24, 2026

    • Successfully obtained differential amplitude images.
    • Successfully obtained differential phase images by controlling phase delay.
    • Presented differential images of a specimen with sharp edges, showcasing both amplitude and phase reflectivity.

    Conclusions:

    • The proposed two-mode optical fiber technique is effective for generating differential amplitude and phase images in scanning microscopy.
    • This technique offers a novel approach to enhance imaging contrast and detail retrieval.