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

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.
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...
Total Internal Reflection Fluorescence Microscopy01:05

Total Internal Reflection Fluorescence Microscopy

Total internal reflection fluorescence microscopy or TIRF is an advanced microscopic technique used to visualize fluorophores in samples close to a solid surface with a higher refractive index, such as a glass coverslip. TIRF only allows fluorophores in proximity to the solid surface to be excited. When light from a medium with a lower refractive index (such as air) hits the glass coverslip at a critical angle, the light undergoes total internal reflection stead of passing through the glass.
Two-Dimensional Microscopy in Microbiology01:29

Two-Dimensional Microscopy in Microbiology

Two-dimensional (2D) microscopy encompasses a range of optical techniques that capture images within a single focal plane, offering detailed representations of microscopic structures. These techniques are essential in biological and medical research, enabling the visualization of cellular and subcellular structures with different levels of contrast and specificity.There are several major types of 2D microscopy, each with strengths and applications.Bright-Field MicroscopyBright-field microscopy...
Imaging Biological Samples with Optical Microscopy01:18

Imaging Biological Samples with Optical Microscopy

Optical microscopy uses optic principles to provide detailed images of samples. Antonie van Leeuwenhoek designed the first compound optical microscope in the 17th century to visualize blood cells, bacteria, and yeast cells. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes with enhanced magnification and resolution.
In optical microscopy, the specimen to be viewed is placed on a glass slide and clipped on the stage...

You might also read

Related Articles

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

Sort by
Same author

Necroptosis triggers inflammatory interferon signatures in patient-derived metastatic breast cancer organoids.

Signal transduction and targeted therapy·2026
Same author

Corrigendum to "Biglycan evokes autophagy in macrophages via a novel CD44/Toll-like receptor 4 signaling axis in ischemia/reperfusion injury." Kidney International 2019;95:540-562.

Kidney international·2026
Same author

Fifty high-content light sheet fluorescence microscopy datasets of Tribolium castaneum embryogenesis.

Scientific data·2025
Same author

Spatiotemporal segmentation of contraction waves in the extra-embryonic membranes of the red flour beetle.

BMC bioinformatics·2025
Same author

Long-term fluorescence live imaging of honeybee embryos using light sheet fluorescence microscopy and halocarbon-based liquids.

Biology open·2025
Same author

Gravitational forces and matrix stiffness modulate the invasiveness of breast cancer cells in bioprinted spheroids.

Materials today. Bio·2025

Related Experiment Video

Updated: Jul 14, 2026

Conducting Multiple Imaging Modes with One Fluorescence Microscope
08:32

Conducting Multiple Imaging Modes with One Fluorescence Microscope

Published on: October 28, 2018

Lateral modulation boosts image quality in single plane illumination fluorescence microscopy.

Tobias Breuninger1, Klaus Greger, Ernst H K Stelzer

  • 1Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, Meyerhofstrasse 1, D-69117 Heidelberg, Germany.

Optics Letters
|July 3, 2007
PubMed
Summary

This study introduces a novel light sheet microscope that enhances image quality by combining structured illumination with optical sectioning. The new technique improves contrast and resolution in scattering fluorescent specimens, enabling clearer visualization of biological structures.

More Related Videos

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy
12:51

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy

Published on: December 9, 2013

Single Plane Illumination Module and Micro-capillary Approach for a Wide-field Microscope
08:53

Single Plane Illumination Module and Micro-capillary Approach for a Wide-field Microscope

Published on: August 15, 2014

Related Experiment Videos

Last Updated: Jul 14, 2026

Conducting Multiple Imaging Modes with One Fluorescence Microscope
08:32

Conducting Multiple Imaging Modes with One Fluorescence Microscope

Published on: October 28, 2018

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy
12:51

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy

Published on: December 9, 2013

Single Plane Illumination Module and Micro-capillary Approach for a Wide-field Microscope
08:53

Single Plane Illumination Module and Micro-capillary Approach for a Wide-field Microscope

Published on: August 15, 2014

Area of Science:

  • Microscopy
  • Optical Imaging
  • Biotechnology

Background:

  • Scattering fluorescent specimens present challenges for high-resolution imaging.
  • Traditional microscopy techniques struggle to achieve optimal contrast and resolution in complex biological samples.

Purpose of the Study:

  • To develop and demonstrate a new microscopy technique for improved imaging of scattering fluorescent specimens.
  • To enhance image contrast and resolution by discriminating against specimen-induced optical artifacts.

Main Methods:

  • A novel microscope combining single light sheet fluorophore excitation with structured illumination was developed.
  • Images were acquired from scattering fluorescent specimens using laterally intensity-modulated light sheets.
  • A data processing scheme was applied to identify nonmodulated volumes and suppress blurred features.

Main Results:

  • The developed technique successfully improved image contrast and resolution.
  • Blurred features in the images were effectively darkened, enhancing clarity.
  • The microscope demonstrated the ability to differentiate image contributions from the specimen's optical properties.

Conclusions:

  • The new microscope effectively overcomes imaging limitations in scattering fluorescent specimens.
  • This technique offers a significant advancement in visualizing complex biological structures with high fidelity.
  • The demonstrated application in imaging Drosophila melanogaster highlights its potential for biological research.