Combs Christian A, Shroff Hari
NHLBI Light Microscopy Facility, National Institutes of Health, Bethesda, Maryland.
NIBIB Section on High Resolution Optical Imaging, National Institutes of Health, Bethesda, Maryland.
Curr Protoc Neurosci. 2017 Apr 10;79:2.1.1-2.1.25. doi: 10.1002/cpns.29.
The field of fluorescence microscopy is rapidly growing and offers ever more imaging capabilities for biologists. Over the past decade, many new technologies and techniques have been developed that allow for combinations of deeper, faster, and higher resolution imaging. These have included the commercialization of many super-resolution and light sheet fluorescence microscopy techniques. For the non-expert, it can be difficult to match the best imaging techniques to biological questions. Picking the most appropriate imaging modality requires a basic understanding of the underlying physics governing each of them, as well as information comparing potentially competing imaging properties in the context of the sample to be imaged. To address these issues, we provide here concise descriptions of a wide range of commercially available imaging techniques from wide-field to super-resolution microscopy, and provide a tabular guide to aid in comparisons among them. In this manner we provide a concise guide to understanding and matching the correct imaging modality to meet research needs. © 2017 by John Wiley & Sons, Inc.
荧光显微镜领域正在迅速发展,为生物学家提供了越来越多的成像能力。在过去十年中,已经开发出许多新技术和方法,实现了更深、更快、更高分辨率成像的组合。其中包括许多超分辨率和光片荧光显微镜技术的商业化。对于非专业人士来说,很难将最佳成像技术与生物学问题相匹配。选择最合适的成像方式需要对每种技术背后的基础物理学有基本的了解,以及在待成像样本的背景下比较潜在竞争成像特性的信息。为了解决这些问题,我们在此简要描述了从宽场显微镜到超分辨率显微镜的各种商用成像技术,并提供了一个表格指南以帮助进行它们之间的比较。通过这种方式,我们提供了一个简明指南,以理解并匹配正确的成像方式来满足研究需求。© 2017 约翰威立父子出版公司