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.
Protein Dynamics in Living Cells01:19

Protein Dynamics in Living Cells

Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...

You might also read

Related Articles

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

Sort by
Same author

Black Hole Spectroscopy and Tests of General Relativity with GW250114.

Physical review letters·2026
Same author

Insecticide Resistance Alters Oviposition Preference in <i>Drosophila melanogaster</i>.

Ecology and evolution·2026
Same author

GW250114: Testing Hawking's Area Law and the Kerr Nature of Black Holes.

Physical review letters·2025
Same author

miR-210 overexpression increases pressure overload-induced cardiac fibrosis.

Non-coding RNA research·2025
Same author

Frequency-Dependent Squeezed Vacuum Source for the Advanced Virgo Gravitational-Wave Detector.

Physical review letters·2023
Same author

Distinguishable DNA methylation defines a cardiac-specific epigenetic clock.

Clinical epigenetics·2023

Related Experiment Video

Updated: May 25, 2026

Computed Tomography-guided Time-domain Diffuse Fluorescence Tomography in Small Animals for Localization of Cancer Biomarkers
12:24

Computed Tomography-guided Time-domain Diffuse Fluorescence Tomography in Small Animals for Localization of Cancer Biomarkers

Published on: July 17, 2012

Perturbative forward solver software for small localized fluorophores in tissue.

F Martelli1, S Del Bianco, P Di Ninni

  • 1Dipartimento di Fisica e Astronomia dell’Universit`a degli Studi di Firenze,Via G. Sansone 1, 50019 Sesto Fiorentino, Firenze, Italy. fabrizio.martelli@unifi.it

Biomedical Optics Express
|January 19, 2012
PubMed
Summary

This study introduces novel software for simulating fluorescent biological tissues using the Born approximation. The tool models photon migration and calculates optical properties like reflectance and transmittance.

Keywords:
(170.3660) Light propagation in tissues(170.3880) Medical and biological imaging(170.5280) Photon migration(170.6280) Spectroscopy, fluorescence and luminescence

More Related Videos

Production and Multi-Parameter Live Cell Fluorescence Lifetime Imaging Microscopy (FLIM) of Multicellular Spheroids
08:43

Production and Multi-Parameter Live Cell Fluorescence Lifetime Imaging Microscopy (FLIM) of Multicellular Spheroids

Published on: August 9, 2024

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

Related Experiment Videos

Last Updated: May 25, 2026

Computed Tomography-guided Time-domain Diffuse Fluorescence Tomography in Small Animals for Localization of Cancer Biomarkers
12:24

Computed Tomography-guided Time-domain Diffuse Fluorescence Tomography in Small Animals for Localization of Cancer Biomarkers

Published on: July 17, 2012

Production and Multi-Parameter Live Cell Fluorescence Lifetime Imaging Microscopy (FLIM) of Multicellular Spheroids
08:43

Production and Multi-Parameter Live Cell Fluorescence Lifetime Imaging Microscopy (FLIM) of Multicellular Spheroids

Published on: August 9, 2024

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

Area of Science:

  • Biomedical Optics
  • Computational Biology
  • Photonic Imaging

Background:

  • Accurate simulation of fluorescence in biological tissues is crucial for diagnostic imaging.
  • Existing models often struggle with localized fluorophores and complex photon migration.
  • The Born approximation offers a computationally tractable approach for scattering media.

Purpose of the Study:

  • To develop and present a forward solver software for simulating fluorescence in biological tissues.
  • To model photon migration from source to fluorophore and from fluorophore to detector.
  • To provide calculable optical properties like reflectance, transmittance, and fluence rate.

Main Methods:

  • Utilized the Born approximation for simulating localized fluorophores in non-fluorescent tissue.
  • Employed a mathematical model for photon migration in both time and continuous wave (CW) domains.
  • Developed FORTRAN subroutines for calculating fluorescent signals in infinite and slab geometries.

Main Results:

  • The proposed software enables simulation of fluorescence emission and photon transport.
  • Green's functions are used for geometries where analytical solutions are available.
  • Calculations of reflectance, transmittance, and fluence rate are supported.

Conclusions:

  • The developed software provides a valuable tool for researchers studying fluorescence in biological tissues.
  • The FORTRAN subroutines offer practical implementation for specific geometric configurations.
  • This work advances the simulation capabilities for optical diagnostics and imaging in biology.