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相关概念视频

Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

12.9K
Confocal microscopy is an advanced microscopic technique. The prime advantage of the confocal microscope over other microscopy techniques is its ability to block the out-of-focus light from the illuminated samples using pinholes. It is widely used with fluorescence optics to obtain high-resolution, sharp contrast images. Unlike optical microscopes, confocal microscopes use a focused beam of light laser to scan the entire sample surface at different z-planes. These microscopes are, therefore,...
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Imaging Biological Samples with Optical Microscopy01:18

Imaging Biological Samples with Optical Microscopy

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Optical microscopy uses optic principles to provide detailed images of samples. Antonie van Leeuwenhoek designed the first compound optical microscope in the 17th century to visualize blood cells, bacteria, and yeast cells. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes with enhanced magnification and resolution.
In optical microscopy, the specimen to be viewed is placed on a glass slide and clipped on the stage...
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相关实验视频

Updated: May 23, 2025

Light Sheet-based Fluorescence Microscopy of Living or Fixed and Stained Tribolium castaneum Embryos
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Light Sheet-based Fluorescence Microscopy of Living or Fixed and Stained Tribolium castaneum Embryos

Published on: April 28, 2017

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Luminos:用于双向显微镜的开源软件.

Daniel G Itkis1, F Phil Brooks1, Hunter C Davis1

  • 1Department of Chemistry and Chemical Biology, Harvard University, Cambridge MA 02138.

bioRxiv : the preprint server for biology
|March 10, 2025
PubMed
概括
此摘要是机器生成的。

双向显微镜 (BDM) 需要精确的实验对齐. Luminos是一个开源的 MATLAB 库,为 BDM 提供微秒精确的同步,增强生物研究.

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Open Source High Content Analysis Utilizing Automated Fluorescence Lifetime Imaging Microscopy
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Open Source High Content Analysis Utilizing Automated Fluorescence Lifetime Imaging Microscopy

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Workflow for High-content, Individual Cell Quantification of Fluorescent Markers from Universal Microscope Data, Supported by Open Source Software
09:57

Workflow for High-content, Individual Cell Quantification of Fluorescent Markers from Universal Microscope Data, Supported by Open Source Software

Published on: December 16, 2014

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相关实验视频

Last Updated: May 23, 2025

Light Sheet-based Fluorescence Microscopy of Living or Fixed and Stained Tribolium castaneum Embryos
10:15

Light Sheet-based Fluorescence Microscopy of Living or Fixed and Stained Tribolium castaneum Embryos

Published on: April 28, 2017

10.5K
Open Source High Content Analysis Utilizing Automated Fluorescence Lifetime Imaging Microscopy
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Open Source High Content Analysis Utilizing Automated Fluorescence Lifetime Imaging Microscopy

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Workflow for High-content, Individual Cell Quantification of Fluorescent Markers from Universal Microscope Data, Supported by Open Source Software
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Workflow for High-content, Individual Cell Quantification of Fluorescent Markers from Universal Microscope Data, Supported by Open Source Software

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科学领域:

  • 生物物理学的生物物理.
  • 细胞生物学 细胞生物学
  • 神经科学是一个神经科学.

背景情况:

  • 双向显微镜 (BDM) 能够同时进行光学扰动和信号成像.
  • 精确的刺激和记录的空间和时间对齐对于BDM至关重要.
  • 现有的方法在实现高精度同步方面面临挑战.

研究的目的:

  • 介绍 Luminos,一个开源的 MATLAB 库用于控制 BDM 实验.
  • 为BDM提供模块化和精确同步的控制.
  • 促进BDM技术的开发和应用.

主要方法:

  • 开发了一个名为Luminos的开源 MATLAB 库.
  • 实现了硬件触发的同步,用于刺激,录制和成像通道.
  • 实现了微秒级的计时精度.

主要成果:

  • 路米诺斯为BDM实验提供模块化控制.
  • 该库确保了精确的硬件触发同步,精确度为微秒.
  • 开源代码和文档是公开的.

结论:

  • Luminos为同步BDM实验提供了一个强大的解决方案.
  • 这种工具将加速生物科学跨越双向显微镜的进步.
  • 图书馆的可用性促进了BDM方法的更广泛的采用和发展.