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

13.0K
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,...
13.0K
Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

6.8K
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...
6.8K

You might also read

Related Articles

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

Sort by
Same author

Author Correction: Label-free human skin imaging with enhanced molecular contrast via time-resolved fluorescence and advanced phasor analysis.

Communications biology·2026
Same author

N-acetylcysteine modulates neutrophil-driven immune and metabolic pathways in steatotic liver ischemia-reperfusion injury.

Frontiers in immunology·2026
Same author

Collagen remodeling in murine melanoma therapy response through second-harmonic generation imaging.

Biophotonics discovery·2026
Same author

Label-free human skin imaging with enhanced molecular contrast via time-resolved fluorescence and advanced phasor analysis.

Communications biology·2025
Same author

In vivo human skin imaging: Distinguishing cellular and fibrillar components with fluorescence lifetime microscopy.

The Journal of investigative dermatology·2025
Same author

Quantum-enhanced detection of viral cDNA via luminescence resonance energy transfer using upconversion and gold nanoparticles.

Nanophotonics (Berlin, Germany)·2025
Same journal

Genetic Impacts on Variability of Body Fat Distribution Uncover Gene-Environment and Gene-Gene Interactions.

bioRxiv : the preprint server for biology·2026
Same journal

16S ribosomal RNA modification drives transcript-specific translation efficiency.

bioRxiv : the preprint server for biology·2026
Same journal

FlcE latches onto the FliL-stator complex to turbocharge flagellar motility in <i>Borrelia burgdorferi</i>.

bioRxiv : the preprint server for biology·2026
Same journal

Synaptic pruning, myelination and the emergence of psychiatric disorders in late adolescence.

bioRxiv : the preprint server for biology·2026
Same journal

Structural and functional insights into the Rcs phosphorelay.

bioRxiv : the preprint server for biology·2026
Same journal

The structural basis of RanGAP1 regulation and catalysis in nuclear transport.

bioRxiv : the preprint server for biology·2026
See all related articles

Related Experiment Video

Updated: May 26, 2025

Open Source High Content Analysis Utilizing Automated Fluorescence Lifetime Imaging Microscopy
09:30

Open Source High Content Analysis Utilizing Automated Fluorescence Lifetime Imaging Microscopy

Published on: January 18, 2017

11.9K

GSLab: Open-Source Platform for Advanced Phasor Analysis in Fluorescence Microscopy.

Alexander Vallmitjana1, Belén Torrado1, Amanda F Durkin1

  • 1Beckman Laser Institute and Medical Clinic, University of California, Irvine.

Biorxiv : the Preprint Server for Biology
|February 24, 2025
PubMed
Summary
This summary is machine-generated.

GSLab offers an open-source platform for fluorescence microscopy image analysis, enhancing phasor analysis with machine learning and quantitative unmixing. This tool aids researchers in complex biological problem-solving.

More Related Videos

Author Spotlight: Standardizing Spheroid Formation Methods for Metabolic and Oxygenation Analysis Using Fluorescence Lifetime Imaging Microscopy
08:43

Author Spotlight: Standardizing Spheroid Formation Methods for Metabolic and Oxygenation Analysis Using Fluorescence Lifetime Imaging Microscopy

Published on: August 9, 2024

795
From Fast Fluorescence Imaging to Molecular Diffusion Law on Live Cell Membranes in a Commercial Microscope
15:10

From Fast Fluorescence Imaging to Molecular Diffusion Law on Live Cell Membranes in a Commercial Microscope

Published on: October 9, 2014

11.4K

Related Experiment Videos

Last Updated: May 26, 2025

Open Source High Content Analysis Utilizing Automated Fluorescence Lifetime Imaging Microscopy
09:30

Open Source High Content Analysis Utilizing Automated Fluorescence Lifetime Imaging Microscopy

Published on: January 18, 2017

11.9K
Author Spotlight: Standardizing Spheroid Formation Methods for Metabolic and Oxygenation Analysis Using Fluorescence Lifetime Imaging Microscopy
08:43

Author Spotlight: Standardizing Spheroid Formation Methods for Metabolic and Oxygenation Analysis Using Fluorescence Lifetime Imaging Microscopy

Published on: August 9, 2024

795
From Fast Fluorescence Imaging to Molecular Diffusion Law on Live Cell Membranes in a Commercial Microscope
15:10

From Fast Fluorescence Imaging to Molecular Diffusion Law on Live Cell Membranes in a Commercial Microscope

Published on: October 9, 2014

11.4K

Area of Science:

  • Biophysics
  • Microscopy
  • Computational Biology

Background:

  • Effective image analysis is crucial for fluorescence microscopy.
  • Traditional phasor analysis has limitations in complex biological samples.
  • Need for advanced, accessible tools in fluorescence imaging.

Purpose of the Study:

  • To introduce GSLab, an open-source platform for advanced phasor analysis in fluorescence microscopy.
  • To enhance traditional phasor analysis with machine learning and quantitative unmixing.
  • To provide researchers with comprehensive tools for complex biological imaging challenges.

Main Methods:

  • Development of an open-source software platform, GSLab.
  • Integration of machine learning-based clustering for phasor data.
  • Implementation of real-time monitoring and quantitative unmixing algorithms.
  • Compatibility with commercial and custom fluorescence microscopy systems.

Main Results:

  • GSLab enhances traditional phasor analysis with advanced computational tools.
  • The platform enables machine learning-based clustering of fluorescence lifetime and spectral data.
  • Quantitative unmixing of fluorescent species is achieved through GSLab's features.
  • Real-time monitoring capabilities improve experimental workflow.

Conclusions:

  • GSLab provides a powerful, open-source solution for fluorescence microscopy image analysis.
  • The platform empowers researchers to address complex biological questions using advanced phasor analysis.
  • GSLab facilitates deeper insights into biological systems through enhanced imaging techniques.