Two-color two-photon 4Pi fluorescence microscopy

被引:20
作者
Chen, JF
Midorikawa, K
机构
[1] RIKEN, Laser Technol Lab, Wako, Saitama 3510198, Japan
[2] Saitama Univ, Saitama City, Saitama 3388570, Japan
关键词
D O I
10.1364/OL.29.001354
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
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. (C) 2004 Optical Society of America.
引用
收藏
页码:1354 / 1356
页数:3
相关论文
共 12 条
[11]   4Pi-confocal imaging in fixed biological specimens [J].
Schrader, M ;
Bahlmann, K ;
Giese, G ;
Hell, SW .
BIOPHYSICAL JOURNAL, 1998, 75 (04) :1659-1668
[12]   FUNDAMENTAL REDUCTION OF THE OBSERVATION VOLUME IN FAR-FIELD LIGHT-MICROSCOPY BY DETECTION ORTHOGONAL TO THE ILLUMINATION AXIS - CONFOCAL THETA MICROSCOPY [J].
STELZER, EHK ;
LINDEK, S .
OPTICS COMMUNICATIONS, 1994, 111 (5-6) :536-547