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Two-Photon Excitation for Optical Nanoscopy and Light-Sheet Illumination Microscopy

机译:光学纳米显微镜和光片照明显微镜的双光子激发

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We report about coupling two-photon excitation (2PE) with two, comparatively young and successful optical methods specially realized for the improvement of resolution and 3D imaging of large samples, i.e. STED (stimulated emission depletion) and SPI (selective plane illumination) microscopy. In the former case we aimed to get a better resolution for 2PE microscopy while for the latter we aimed to obtain better penetration in scattering samples by shifting the light sheet wavelengths to the red in the non-linear domain. We show results obtained by adapting a commercial STED-CW microscope to 2PE and by implementing a 2PE-SPIM homemade system. The implementation of these systems is demonstrated by the imaging of living Saccharomyces cervisiae cells.
机译:我们报告了将双光子激发(2PE)与两个特别年轻的成功光学方法耦合在一起的方法,这些方法专门用于提高大样本的分辨率和3D成像,即STED(受激发射损耗)和SPI(选择性平面照明)显微镜。在前一种情况下,我们旨在为2PE显微镜获得更好的分辨率,而在后一种情况下,我们旨在通过在非线性域中将光片波长偏移为红色来在散射样品中获得更好的穿透力。我们展示了通过将商用STED-CW显微镜适应2PE并实现2PE-SPIM自制系统而获得的结果。这些系统的实现通过活酿酒酵母细胞的成像证明。

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