Related Experiment Video
Updated: Apr 8, 2026

Visualization of the Immunological Synapse by Dual Color Time-gated Stimulated Emission Depletion STED Nanoscopy
Published on: March 24, 2014
Resonant-scanning dual-color STED microscopy with ultrafast photon counting: A concise guide
Yong Wu1, Xundong Wu2, Ligia Toro3
1Division of Molecular Medicine, Department of Anesthesiology, David Geffen School of Medicine, UCLA, United States; Cardiovascular Research Laboratory, David Geffen School of Medicine, UCLA, United States.
Abstract:
STED (stimulated emission depletion) is a popular super-resolution fluorescence microscopy technique. In this paper, we present a concise guide to building a resonant-scanning STED microscope with ultrafast photon-counting acquisition. The STED microscope has two channels, using a pulsed laser and a continuous-wave (CW) laser as the depletion laser source, respectively. The CW STED channel preforms time-gated detection to enhance optical resolution in this channel. We use a resonant mirror to attain high scanning speed and ultrafast photon counting acquisition to scan a large field of view, which help reduce photobleaching. We discuss some practical issues in building a STED microscope, including creating a hollow depletion beam profile, manipulating polarization, and monitoring optical aberration. We also demonstrate a STED image enhancement method using stationary wavelet expansion and image analysis methods to register objects and to quantify colocalization in STED microscopy.
More Related Videos
Related Concept Videos
Super-resolution Fluorescence Microscopy
Confocal Fluorescence Microscopy

