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Updated: Aug 25, 2026

Conducting Multiple Imaging Modes with One Fluorescence Microscope
Published on: October 28, 2018
Conversion of the Nikon C1 confocal laser-scanning head for multiphoton excitation on an upright microscope
Andrew Ridsdale1, Ileana Micu, Peter K Stys
1Neuroscience Unit, Ottawa Health Research Institute, 725 Parkdale Avenue, Ottawa, Canada. aridsdale@ohri.ca
Abstract:
Most commercial laser-scanning imaging systems used for confocal fluorescence microscopy can be readily adapted for use with two-photon fluorescence excitation. We report here on the details of the conversion of the Nikon C1 (product released November 2001) with two channels of nondescanned detection of two-photon-excited fluorescence. One of the goals of the design was to utilize off-the-shelf components as much as possible to minimize the use of custom machining and electronics assembly. We also give some initial characterization of the imaging properties of the system.

