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使用加速光束的单光子和双光子集成光片显微镜。

Integrated single- and two-photon light sheet microscopy using accelerating beams.

机构信息

SUPA, School of Physics and Astronomy, University of St Andrews, North Haugh, St Andrews, KY16 9SS, UK.

Institute of Physics, University of Tartu, W. Ostwald St 1, Tartu, 50411, Estonia.

出版信息

Sci Rep. 2017 May 3;7(1):1435. doi: 10.1038/s41598-017-01543-4.

DOI:10.1038/s41598-017-01543-4
PMID:28469191
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5431168/
Abstract

We demonstrate the first light sheet microscope using propagation invariant, accelerating Airy beams that operates both in single- and two-photon modes. The use of the Airy beam permits us to develop an ultra compact, high resolution light sheet system without beam scanning. In two-photon mode, an increase in the field of view over the use of a standard Gaussian beam by a factor of six is demonstrated. This implementation for light sheet microscopy opens up new possibilities across a wide range of biomedical applications, especially for the study of neuronal processes.

摘要

我们展示了第一台使用传播不变、加速的艾里光束的光片显微镜,该显微镜可在单光子和双光子模式下工作。艾里光束的使用使我们能够开发出一种超紧凑、高分辨率的光片系统,而无需光束扫描。在双光子模式下,与使用标准高斯光束相比,视场增加了六倍。这种用于光片显微镜的实现为广泛的生物医学应用开辟了新的可能性,特别是在神经元过程的研究方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/3de78e1ed0c8/41598_2017_1543_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/ef278319c419/41598_2017_1543_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/25b4b903c7e1/41598_2017_1543_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/91429a25b001/41598_2017_1543_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/437a510fcf3f/41598_2017_1543_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/530356d7f372/41598_2017_1543_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/404b1e05ace5/41598_2017_1543_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/3de78e1ed0c8/41598_2017_1543_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/ef278319c419/41598_2017_1543_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/25b4b903c7e1/41598_2017_1543_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/91429a25b001/41598_2017_1543_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/437a510fcf3f/41598_2017_1543_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/530356d7f372/41598_2017_1543_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/404b1e05ace5/41598_2017_1543_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/5431168/3de78e1ed0c8/41598_2017_1543_Fig7_HTML.jpg

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Dynamic structure and protein expression of the live embryonic heart captured by 2-photon light sheet microscopy and retrospective registration.通过双光子光片显微镜和回顾性配准捕获的活胚胎心脏的动态结构和蛋白质表达。
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Bessel Beam Illumination Reduces Random and Systematic Errors in Quantitative Functional Studies Using Light-Sheet Microscopy.贝塞尔光束照明减少了使用光片显微镜进行定量功能研究中的随机误差和系统误差。
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