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 Experiment Videos

Raising the speed limits for 4D fluorescence microscopy.

A T Hammond1, B S Glick

  • 1Department of Molecular Genetics and Cell Biology, University of Chicago, 920 East 58th Street, Chicago, IL 60637, USA.

Traffic (Copenhagen, Denmark)
|February 24, 2001
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Crosslinking a lipid raft component triggers liquid ordered-liquid disordered phase separation in model plasma membranes.

Proceedings of the National Academy of Sciences of the United States of America·2005
Same author

Tagging Hansenula polymorpha genes by random integration of linear DNA fragments (RALF).

Molecular genetics and genomics : MGG·2002
Same author

Deconstructing Golgi inheritance.

Traffic (Copenhagen, Denmark)·2001
Same author

Vector for pop-in/pop-out gene replacement in Pichia pastoris.

BioTechniques·2001
Same author

ER export: more than one way out.

Current biology : CB·2001
Same author

A role for actin, Cdc1p, and Myo2p in the inheritance of late Golgi elements in Saccharomyces cerevisiae.

The Journal of cell biology·2001

Four-dimensional (4D) fluorescence microscopy, a routine experimental tool, is enhanced by a new method for speeding image acquisition in 4D confocal microscopy. This advancement improves 4D microscopy technologies.

Area of Science:

  • Cell biology
  • Microscopy
  • Biotechnology

Background:

  • Three-dimensional time-lapse (4D) fluorescence microscopy is increasingly utilized in biological research.
  • Existing 4D microscopy techniques face challenges with image acquisition speed.

Purpose of the Study:

  • To review current technologies in 4D fluorescence microscopy.
  • To introduce a novel method for accelerating image acquisition in 4D confocal microscopy.

Main Methods:

  • Literature review of existing 4D microscopy technologies.
  • Description of a new method for enhancing image acquisition speed in 4D confocal microscopy.

Main Results:

  • Summary of current state-of-the-art 4D fluorescence microscopy.

Related Experiment Videos

  • Introduction of a method to improve the efficiency of 4D confocal microscopy.

    • Conclusions:

    • 4D fluorescence microscopy is a vital tool in modern science.
    • The described method offers a significant improvement for 4D confocal microscopy applications.