Kromm D, Thumberger T, Wittbrodt J
Centre for Organismal Studies, Heidelberg University, Heidelberg, Germany.
Methods Cell Biol. 2016;133:105-23. doi: 10.1016/bs.mcb.2016.01.001. Epub 2016 Feb 27.
This chapter introduces the principles and advantages of selective plane illumination microscopy (SPIM) and compares it to commonly used epifluorescence or confocal setups. Due to the low phototoxicity, speed of imaging, high penetration depth, and spatiotemporal resolution, SPIM is predestined for in vivo imaging but can as well be used for in toto analysis of large fixed samples. Key points of light-sheet microscopy are highlighted and discussed priming the investigator to choose the best suitable system from the large collection of possible SPIM setups. Mounting of samples is shown and the demands for data acquisition, processing, handling, and visualization are discussed.
本章介绍了选择性平面照明显微镜(SPIM)的原理和优势,并将其与常用的落射荧光或共聚焦装置进行比较。由于光毒性低、成像速度快、穿透深度高以及时空分辨率高,SPIM注定适用于体内成像,但也可用于对大型固定样本进行整体分析。突出并讨论了光片显微镜的要点,引导研究人员从大量可能的SPIM装置中选择最合适的系统。展示了样本的安装,并讨论了数据采集、处理、处理和可视化的要求。
Methods Cell Biol. 2016
Development. 2009-6
Curr Protoc Cytom. 2015-1-5
Development. 2021-9-15
Methods Cell Biol. 2014
Nat Methods. 2012-6-3
Front Cell Dev Biol. 2021-7-26
J Comp Neurol. 2021-3