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相关概念视频

Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

13.4K
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,...
13.4K
Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

7.0K
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
7.0K
Phase Contrast and Differential Interference Contrast Microscopy01:26

Phase Contrast and Differential Interference Contrast Microscopy

8.2K
Phase-Contrast Microscopes
In-phase-contrast microscopes, interference between light directly passing through a cell and light refracted by cellular components is used to create high-contrast, high-resolution images without staining. It is the oldest and simplest type of microscope that creates an image by altering the wavelengths of light rays passing through the specimen. Altered wavelength paths are created using an annular stop in the condenser. The annular stop produces a hollow cone of...
8.2K

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相关实验视频

Updated: Jul 17, 2025

Near Simultaneous Laser Scanning Confocal and Atomic Force Microscopy Conpokal on Live Cells
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Near Simultaneous Laser Scanning Confocal and Atomic Force Microscopy Conpokal on Live Cells

Published on: August 11, 2020

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在相位解析的共聚焦显微镜中进行计算重定焦.

Martin Schnell, Melanie King, Sam Buercklin

    Optics letters
    |September 1, 2023
    PubMed
    概括
    此摘要是机器生成的。

    我们展示了如何使用合成全息学在连贯的共聚焦激光扫描显微镜中数字重新聚焦图像. 这种基于物理学的方法从多个焦平面数据中计算重建了对焦图像,这对于表面造型有用.

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    Conducting Multiple Imaging Modes with One Fluorescence Microscope
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    相关实验视频

    Last Updated: Jul 17, 2025

    Near Simultaneous Laser Scanning Confocal and Atomic Force Microscopy Conpokal on Live Cells
    09:20

    Near Simultaneous Laser Scanning Confocal and Atomic Force Microscopy Conpokal on Live Cells

    Published on: August 11, 2020

    6.9K
    Conducting Multiple Imaging Modes with One Fluorescence Microscope
    08:32

    Conducting Multiple Imaging Modes with One Fluorescence Microscope

    Published on: October 28, 2018

    9.9K
    Video-rate Scanning Confocal Microscopy and Microendoscopy
    14:10

    Video-rate Scanning Confocal Microscopy and Microendoscopy

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    科学领域:

    • 光学和光子学 在光学和光子学.
    • 显微镜技术 显微镜技术
    • 计算成像技术的成像

    背景情况:

    • 同焦激光扫描显微镜 (CLSM) 提供高分辨率的光学切割.
    • 在具有显著地形变异的样本中实现对焦仍然是CLSM的一个挑战.
    • 合成光学全息提供了一种捕获复杂波浪信息的方法.

    研究的目的:

    • 用合成光学全息图来证明在连贯的CLSM中的数值重定位.
    • 为了验证基于物理的计算传播方法用于图像重建.
    • 探索复杂样品的高分辨率表面造型的应用.

    主要方法:

    • 在合成全息的复杂信号上实现计算波传播.
    • 在多个焦平面偏移处获取CLSM数据.
    • 通过纠正焦点偏差来重建对焦图像.

    主要成果:

    • 从多焦平面数据成功恢复了测试对象的焦点图像.
    • 在一个连贯的CLSM设置中证明了数值重定位的可行性.
    • 验证了基于物理的计算传播模型的准确性.

    结论:

    • 基于合成全息的数值重定位是CLSM的一种可行的技术.
    • 这种方法可以获得高度差异很大的样本的聚焦视图.
    • 潜在的应用包括先进的共聚焦光学表面造型.