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Related Concept Videos

Total Internal Reflection Fluorescence Microscopy01:05

Total Internal Reflection Fluorescence Microscopy

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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.
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Super-resolution Fluorescence Microscopy01:37

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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...
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Related Experiment Video

Updated: Jul 29, 2025

Fluorescence Lifetime Macro Imager for Biomedical Applications
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Fluorescence Lifetime Macro Imager for Biomedical Applications

Published on: April 7, 2023

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Light-field tomographic fluorescence lifetime imaging microscopy.

Yayao Ma1, Luzhe Huang1,2,3, Chandani Sen4

  • 1Department of Bioengineering, University of California, Los Angeles, CA, USA.

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|May 22, 2023
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Summary
This summary is machine-generated.

Light field tomographic FLIM (LIFT-FLIM) accelerates 3D imaging by reducing scanning steps. This novel computational technique enhances molecular-level biological visualization and data acquisition efficiency.

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Last Updated: Jul 29, 2025

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Area of Science:

  • Biophotonics
  • Molecular Imaging
  • Computational Microscopy

Background:

  • Fluorescence Lifetime Imaging Microscopy (FLIM) visualizes biological samples at the molecular level.
  • Conventional FLIM faces challenges with long acquisition times, especially for 3D imaging, due to extensive scanning.
  • High-resolution lifetime mapping is crucial for understanding molecular interactions and cellular environments.

Conclusions:

  • LIFT-FLIM offers a highly data-efficient method for volumetric fluorescence lifetime imaging.
  • The technique enhances speed and sensitivity, enabling advanced biological research.
  • LIFT-FLIM has potential applications in basic and translational biomedical research.