首页> 外文会议> >Breaking the diffraction limit in far-field light microscopy by stimulated emission
【24h】

Breaking the diffraction limit in far-field light microscopy by stimulated emission

机译:受激发射打破了远场光学显微镜中的衍射极限

获取原文

摘要

Summary form only given. The advantage of far-field light microscopy over electron, X-ray, or scanning probe microscopes is the non-destructive imaging of the interior of biological specimens. In fact, focused light is the only means to visualise living biological specimens at the submicron scale in three dimensions. Not surprisingly, far-field light microscopy is still the most popular form of microscopy in biomedical research, whereby 80% of the observations are based on fluorescence. An obvious disadvantage of using focused light is the limited spatial resolution, which for more than a century has been paradigmatic. The best resolving far-field light microscopes, the laser scanning confocal and multiphoton excitation microscope enjoy increasing popularity both in biomedicine as well as in single molecule spectroscopy, however, the best resolution they can achieve is 200 nm in the lateral and 500 nm in the axial directions.
机译:仅提供摘要表格。远场光学显微镜优于电子,X射线或扫描探针显微镜的优点是生物标本内部的非破坏性成像。实际上,聚焦光是在三个维度上以亚微米级可视化活生物标本的唯一方法。毫不奇怪,远场光学显微镜仍然是生物医学研究中最流行的显微镜形式,其中80%的观察结果基于荧光。使用聚焦光的一个明显缺点是空间分辨率有限,这在一个多世纪以来一直是范式。最好的分辨远场光学显微镜,激光扫描共聚焦和多光子激发显微镜在生物医学和单分子光谱学中都越来越受欢迎,但是,它们可以实现的最佳分辨率是横向200 nm,横向500 nm。轴向。

著录项

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