下载PDF
{"title":"Fluorescence Microscopy: A Concise Guide to Current Imaging Methods","authors":"Christian A. Combs, Hari Shroff","doi":"10.1002/cpns.29","DOIUrl":null,"url":null,"abstract":"<p>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.</p>","PeriodicalId":40016,"journal":{"name":"Current Protocols in Neuroscience","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2018-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpns.29","citationCount":"158","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Neuroscience","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpns.29","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Neuroscience","Score":null,"Total":0}
引用次数: 158
引用
批量引用
Abstract
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:当前成像方法的简明指南
荧光显微镜领域正在迅速发展,为生物学家提供了更多的成像能力。在过去的十年中,已经开发了许多新技术和技术,可以实现更深、更快和更高分辨率的成像。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,很难将最好的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控制每种成像方式的潜在物理原理有基本的了解,以及在待成像样品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,我们在这里提供了从宽视场到超分辨率显微镜的广泛的商业可用成像技术的简明描述,并提供了一个表格指南,以帮助他们之间的比较。通过这种方式,我们提供了一个简明的指南来理解和匹配正确的成像方式,以满足研究需求。©2017 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。