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

Protein Dynamics in Living Cells01:19

Protein Dynamics in Living Cells

2.1K
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...
2.1K
Total Internal Reflection Fluorescence Microscopy01:05

Total Internal Reflection Fluorescence Microscopy

5.6K
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.
5.6K

You might also read

Related Articles

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

Sort by
Same author

Mitochondria power the cell's recycling center.

Autophagy·2026
Same author

Mitochondria acidify lysosomes through membrane contacts.

Cell reports·2026
Same author

Mechanisms of Fusion Protein Transmembrane Segments in Fusion Pore Formation.

Chembiochem : a European journal of chemical biology·2026
Same author

Cycling molecular assemblies for Golgi imaging and disruption.

Nature communications·2026
Same author

Cholesterol modulates vesicle clustering mediated by alpha-synuclein in a nonlinear fashion.

Biophysics reports·2026
Same author

Munc18 modulates syntaxin phase separation to promote exocytosis.

Nature neuroscience·2025

Related Experiment Video

Updated: Jun 6, 2025

A Bright NIR-II Fluorescence Probe for Vascular and Tumor Imaging
05:51

A Bright NIR-II Fluorescence Probe for Vascular and Tumor Imaging

Published on: March 17, 2023

1.7K

Near-Infrared Bioimaging Using Two-photon Fluorescent Probes.

Pragti1, Bidyut Kumar Kundu1, Rui Chen1

  • 1Department of Chemistry, University of Cincinnati, Cincinnati, OH, 45221, USA.

Advanced Healthcare Materials
|November 22, 2024
PubMed
Summary

Two-photon absorption (TPA) fluorescent probes offer superior near-infrared (NIR) bioimaging by enhancing tissue penetration and reducing photodamage. Future advancements focus on in vivo applications and dual-function probes for diagnosis and therapy.

Keywords:
bioimagingfluorescent probestwo‐photon absorption

More Related Videos

Automated Two-dimensional Spatiotemporal Analysis of Mobile Single-molecule FRET Probes
08:26

Automated Two-dimensional Spatiotemporal Analysis of Mobile Single-molecule FRET Probes

Published on: November 23, 2021

2.5K
In vivo Imaging of Biological Tissues with Combined Two-Photon Fluorescence and Stimulated Raman Scattering Microscopy
09:06

In vivo Imaging of Biological Tissues with Combined Two-Photon Fluorescence and Stimulated Raman Scattering Microscopy

Published on: December 20, 2021

3.2K

Related Experiment Videos

Last Updated: Jun 6, 2025

A Bright NIR-II Fluorescence Probe for Vascular and Tumor Imaging
05:51

A Bright NIR-II Fluorescence Probe for Vascular and Tumor Imaging

Published on: March 17, 2023

1.7K
Automated Two-dimensional Spatiotemporal Analysis of Mobile Single-molecule FRET Probes
08:26

Automated Two-dimensional Spatiotemporal Analysis of Mobile Single-molecule FRET Probes

Published on: November 23, 2021

2.5K
In vivo Imaging of Biological Tissues with Combined Two-Photon Fluorescence and Stimulated Raman Scattering Microscopy
09:06

In vivo Imaging of Biological Tissues with Combined Two-Photon Fluorescence and Stimulated Raman Scattering Microscopy

Published on: December 20, 2021

3.2K

Area of Science:

  • Biomedical Imaging
  • Optics
  • Materials Science

Background:

  • Near-infrared (NIR) bioimaging is a key technology in biomedical research.
  • Two-photon absorption (TPA) fluorescent probes offer advantages over one-photon absorption (OPA) probes.
  • TPA probes provide enhanced tissue penetration, reduced photodamage, and improved spatial resolution.

Purpose of the Study:

  • To provide a comprehensive overview of TPA fluorescent probes for NIR bioimaging.
  • To discuss fundamental principles, design strategies, and applications of TPA probes.
  • To highlight recent advancements and future perspectives in TPA probe development.

Main Methods:

  • Review of molecular fluorescent probes, including organic, inorganic, and COF/MOF-based systems.
  • Discussion of stimulated TPA probes responsive to environmental factors (pH, redox, enzymes, hypoxia).
  • Analysis of design strategies for TPA probe development.

Main Results:

  • TPA probes demonstrate significant potential for advanced bioimaging applications.
  • Various molecular designs enable tailored TPA probe properties.
  • Stimulated TPA probes offer dynamic and responsive imaging capabilities.

Conclusions:

  • TPA fluorescent probes are crucial for next-generation NIR bioimaging.
  • Further research should focus on in vivo studies and dual-function probes.
  • Development of TPA probes will advance disease diagnosis and therapeutic strategies.