Simultaneous confocal lifetime imaging of multiple fluorophores using the intensity‐modulated multiple‐wavelength scanning (IMS) technique
Author:
Affiliation:
1. Department of Biomedical and X‐ray Physics,
2. Department of Geodesy and Photogrammetry, The Royal Institute of Technology, SE‐100 44 Stockholm, Sweden,
3. Department of Neuroscience, Karolinska Institute, SE‐171 77 Stockholm, Sweden
Publisher
Wiley
Subject
Histology,Pathology and Forensic Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2818.1998.00362.x
Reference17 articles.
1. Confocal scanning microfluorometry of dual-labelled specimens using two excitation wavelengths and lock-in detection technique
2. Fluorescence lifetime imaging using a confocal laser scanning microscope
3. Three-dimensional imaging of neurons by confocal fluorescence microscopy
4. Simultaneous confocal recording of multiple fluorescent labels with improved channel separation
5. Signal-to-noise ratio for confocal microscopy when using the Intensity-modulated Multiple-beam Scanning (IMS) technique
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