Booth M J, Hell S W
High Resolution Optical Microscopy Group, Max-Planck-Institute for Biophysical Chemistry, Göttingen, Germany.
J Microsc. 1998 Jun;190(Pt 3):298-304. doi: 10.1046/j.1365-2818.1998.00375.x.
We report on efficient two-photon fluorescence imaging in beam scanning microscopy by exciting UV dyes at the 647-nm line of a continuous wave ArKr mixed gas laser. For a numerical aperture of 1.4 (oil), we used an illumination power of up to 210 mW at the sample. High-resolution images were obtained for DAPI-labelled cell nuclei within 4-60 s. Our method is a simple two-photon alternative to UV confocal imaging with the potential of becoming a very useful feature of laser scanning microscopy.
我们报告了在光束扫描显微镜中通过在连续波氩氪混合气体激光器的647纳米谱线激发紫外染料来进行高效双光子荧光成像的情况。对于数值孔径为1.4(油浸)的情况,我们在样品处使用了高达210毫瓦的照明功率。在4至60秒内获得了DAPI标记细胞核的高分辨率图像。我们的方法是紫外共聚焦成像的一种简单的双光子替代方法,有潜力成为激光扫描显微镜非常有用的一项功能。