Journal
/
/
Autofluorescence Imaging to Evaluate Cellular Metabolism
JoVE Journal
Bioengineering
A subscription to JoVE is required to view this content.  Sign in or start your free trial.
JoVE Journal Bioengineering
Autofluorescence Imaging to Evaluate Cellular Metabolism
DOI:

07:36 min

November 15, 2021

, , , ,

Chapters

  • 00:04Introduction
  • 01:04Multiphoton Fluorescence Lifetime Imaging (FLIM) of Nicotinamide Adenine (Phosphate) Dinucleotide (NAD(P)H) and Flavin Adenine Dinucleotide (FAD)
  • 02:13Nicotinamide Adenine (Phosphate) Dinucleotide (NAD(P)H) Imaging
  • 03:35Flavin Adenine Dinucleotide (FAD) Imaging
  • 04:45Cyanide Experiment Preparation
  • 05:28Results: The Fluorescence Imaging of MCF-7 Cells Before and After Cyanide Treatment
  • 07:05Conclusion

Summary

Automatic Translation

This protocol describes fluorescence imaging and analysis of the endogenous metabolic coenzymes, reduced nicotinamide adenine (phosphate) dinucleotide (NAD(P)H), and oxidized flavin adenine dinucleotide (FAD). Autofluorescence imaging of NAD(P)H and FAD provides a label-free, nondestructive method to assess cellular metabolism.

Related Videos

Read Article