Two-color two-photon 4Pi fluorescence microscopy
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Updated: Aug 23, 2026

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy
Published on: December 9, 2013
Jianfang Chen1, Katsumi Midorikawa
1Laser Technology Laboratory, RIKEN, Hirosawa 2-1, Wako, Saitama 351-0198, Japan. chen@postman.riken.go.jp
Abstract:
In 4Pi fluorescence microscopy the point-spread function is composed of a strong central lobe accompanied by interference sidelobes that produce artifacts in the image. We propose to combine two-color two-photon fluorescence microscopy and 4Pi fluorescence microscopy to overcome this sidelobe problem. Simulation results show that a single sharp fluorescence spot can be produced by use of two excitation wavelengths of 400 and 800 nm and detected at 350-nm emission wavelength.
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