首页> 外文会议>Conference on Confocal, Multiphoton, and Nonlinear Microscopic Imaging >Simultaneous Imaging of Confocal Fluorescence and Raman Spectrum
【24h】

Simultaneous Imaging of Confocal Fluorescence and Raman Spectrum

机译:共聚焦荧光和拉曼光谱的同时成像

获取原文

摘要

The advantage of confocal fluorescence microscopy is the ability to acquire high resolution images of fluorescent specimens non-invasively. On the other hand, the advantage of Raman microscopy is the ability to provide the chemical characteristics of specimens from spectroscopy. To obtain simultaneously high resolution images and chemical characteristics of specimens, fluorescence signals from stained cell and Raman spectrum from cell itself should be separated. By separating two kinds of signals, confocal fluorescence image and Raman spectrum are acquired simultaneously at the same position. In this paper, we demonstrate a confocal fluorescence microscopy combined with the Raman microscopy. And we propose a method that eliminates Raman spectrum of fluorophore itself from Raman spectrum of the stained cell and that obtains simultaneously confocal fluorescence image from stained cell and Raman spectrum of cell itself without replacing a cell.
机译:共聚焦荧光显微镜的优点是能够获取荧光样品的高分辨率图像无侵入性。另一方面,拉曼显微镜的优点是能够提供来自光谱的样本的化学特性。为了同时获得高分辨率的图像和样本的化学特性,应分离来自染色细胞和来自细胞本身的拉曼光谱的荧光信号。通过分离两种信号,在相同位置同时获取共聚焦荧光图像和拉曼光谱。在本文中,我们证明了与拉曼显微镜相结合的共聚焦荧光显微镜。并且我们提出了一种方法,该方法从染色细胞的拉曼光谱消除荧光团体本身的拉曼光谱,并且在不替换细胞的情况下,从染色的细胞和细胞自身的拉曼光谱获得同时共杂细荧光图像。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号