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用激光薄片轻柔地切割胚胎。

Slicing embryos gently with laser light sheets.

机构信息

Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.

出版信息

Bioessays. 2012 May;34(5):406-11. doi: 10.1002/bies.201100120. Epub 2012 Mar 6.

Abstract

Light sheet microscopy is an easy to implement and extremely powerful alternative to established fluorescence imaging techniques such as laser scanning confocal, multi-photon and spinning disk microscopy. By illuminating the sample only with a thin slice of light, photo-bleaching is reduced to a minimum, making light sheet microscopy ideal for non-destructive imaging of fragile samples over extended periods of time. Millimeter-sized samples can be imaged rapidly with high resolution and high depth penetration. A large variety of instruments have been developed and optimized for a number of different samples: Bessel beams form thin light sheets for single cells, and selective plane illumination microscopy (SPIM) offers multi-view acquisition to image entire embryos with isotropic resolution. This review explains how light sheet microscopy involves a conceptually new microscope design and how it changes modern imaging in biology.

摘要

光片显微镜是一种易于实现且功能强大的替代方法,可以替代已建立的荧光成像技术,如激光扫描共聚焦、多光子和旋转盘显微镜。通过仅用薄光片照射样品,可以将光漂白降至最低,因此光片显微镜非常适合在较长时间内对易碎样品进行非破坏性成像。毫米大小的样品可以快速高分辨率和高深度穿透进行成像。已经开发出了多种仪器,并针对各种不同的样品进行了优化:贝塞尔光束形成用于单细胞的薄光片,选择性平面照明显微镜(SPIM)提供多视图采集,可用于以各向同性分辨率对整个胚胎进行成像。本文综述解释了光片显微镜如何涉及一种新概念的显微镜设计,以及它如何改变生物学中的现代成像。

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