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

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.
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...
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

Celldetective, an AI-enhanced image analysis tool for unraveling dynamic cell interactions.

eLife·2026
Same author

Correlations in cadherin-mediated membrane adhesion dynamics: Molecular concentration switch and diffusion dial.

Biophysical journal·2026
Same author

Quantitative Microscopy for Cell-Surface and Cell-Cell Interactions in Immunology.

Bio-protocol·2025
Same author

Tracing Erich Sackmann's journey from liquid crystals to biological membranes.

Biophysical journal·2025
Same author

Conference Report: Cell Biology and Mechanobiology in Mexico.

Biology of the cell·2025
Same author

Decoupling Individual Host Response and Immune Cell Engager Cytotoxic Potency.

ACS nano·2025

Related Experiment Video

Updated: Jun 19, 2026

Imaging Molecular Adhesion in Cell Rolling by Adhesion Footprint Assay
08:24

Imaging Molecular Adhesion in Cell Rolling by Adhesion Footprint Assay

Published on: September 27, 2021

Quantitative reflection interference contrast microscopy (RICM) in soft matter and cell adhesion.

Laurent Limozin1, Kheya Sengupta

  • 1Adhesion and Inflammation, CNRS UMR 6212, Inserm U600, Aix-Marseille University, Luminy, Marseille, France. laurent.limozin@inserm.fr

Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry
|October 10, 2009
PubMed
Summary

Reflection interference contrast microscopy (RICM) precisely measures adhesion dynamics in soft systems. Recent advancements enhance its application for studying cell and soft matter interactions with nanometric precision.

More Related Videos

Implementation of Interference Reflection Microscopy for Label-free, High-speed Imaging of Microtubules
09:45

Implementation of Interference Reflection Microscopy for Label-free, High-speed Imaging of Microtubules

Published on: August 8, 2019

Visualizing Adhesion Formation in Cells by Means of Advanced Spinning Disk-Total Internal Reflection Fluorescence Microscopy
10:19

Visualizing Adhesion Formation in Cells by Means of Advanced Spinning Disk-Total Internal Reflection Fluorescence Microscopy

Published on: January 21, 2019

Related Experiment Videos

Last Updated: Jun 19, 2026

Imaging Molecular Adhesion in Cell Rolling by Adhesion Footprint Assay
08:24

Imaging Molecular Adhesion in Cell Rolling by Adhesion Footprint Assay

Published on: September 27, 2021

Implementation of Interference Reflection Microscopy for Label-free, High-speed Imaging of Microtubules
09:45

Implementation of Interference Reflection Microscopy for Label-free, High-speed Imaging of Microtubules

Published on: August 8, 2019

Visualizing Adhesion Formation in Cells by Means of Advanced Spinning Disk-Total Internal Reflection Fluorescence Microscopy
10:19

Visualizing Adhesion Formation in Cells by Means of Advanced Spinning Disk-Total Internal Reflection Fluorescence Microscopy

Published on: January 21, 2019

Area of Science:

  • Soft matter physics
  • Biophysics
  • Microscopy techniques

Background:

  • Adhesion quantification requires measuring inter-surface distances.
  • Reflection interference contrast microscopy (RICM) offers nanometric precision and millisecond resolution for studying adhesion dynamics.
  • Soft systems present unique challenges for adhesion studies.

Purpose of the Study:

  • To review the principles and recent developments of RICM for dynamical adhesion studies.
  • To highlight RICM's application in soft matter and cell biology.
  • To provide practical guidance for RICM users.

Main Methods:

  • Utilizing Reflection Interference Contrast Microscopy (RICM) for inter-surface distance measurements.
  • Employing advanced image analysis techniques.
  • Incorporating multi-coloured illumination for enhanced data acquisition.

Main Results:

  • Achieved unambiguous quantitative measurements for colloidal beads and model membranes.
  • Demonstrated RICM's suitability for studying dynamical adhesion processes.
  • Revealed new insights and applications in soft matter and cell biology.

Conclusions:

  • RICM is a powerful technique for quantifying dynamical adhesion in soft systems.
  • Recent technical innovations have revitalized RICM applications.
  • RICM shows significant promise for cell biology research and soft matter studies.