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相关概念视频

Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

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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...
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Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

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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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Overview of Microscopy Techniques01:22

Overview of Microscopy Techniques

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The early pioneers of microscopy opened a window into the invisible world of microorganisms. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes that leveraged nonvisible light, such as fluorescence microscopy that uses an ultraviolet light source and electron microscopy that uses short-wavelength electron beams. These advances significantly improved magnification, image resolution, and contrast. By comparison, the...
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相关实验视频

Updated: May 14, 2025

Multimodal Analytical Platform on a Multiplexed Surface Plasmon Resonance Imaging Chip for the Analysis of Extracellular Vesicle Subsets
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自动聚焦扫描表面等离子体共振显微镜.

Sheng Sun, Pengbin Liu, Jingfang Hu

    Optics express
    |April 12, 2025
    PubMed
    概括

    自动对焦扫描表面等离子体共振显微镜 (SPRM) 在大场成像期间纠正焦点偏移. 这种增强的成像方法提高了生物分子相互作用检测和纳米级观测能力.

    科学领域:

    • 纳米技术纳米技术
    • 生物物理学的生物物理.
    • 显微镜的使用方法

    背景情况:

    • 表面等离子共振显微镜 (SPRM) 对于无标签的生物分子实时纳米成像至关重要.
    • 传统的SPRM具有有限的视野 (FOV),并且在扫描过程中容易引起焦点偏移,降低图像质量.

    研究的目的:

    • 开发一种自动对焦扫描SPRM (AFS-SPRM) 系统,用于实现自动,实时的对焦偏移校正.
    • 为了实现高质量,大FOV SPRM成像,以改善生物分子相互作用研究.

    主要方法:

    • 开发一个集成到扫描SPRM系统中的自动对焦机制.
    • 实现快速 (80毫秒) 失焦事件处理以实时进行焦点校正.

    主要成果:

    • 与传统的SPRM相比,AFS-SPRM系统的焦点稳定性得到了30倍的改善.
    • 成功区分了不同大小的纳米粒子.
    • 在含有纳米粒子的介质中观察到巨细胞的动态变化.

    结论:

    • 通过提供稳定,高质量,大FOV成像,AFS-SPRM克服了传统SPRM的局限性.
    • 该技术显示了纳米级生物分子相互作用研究和实时生物过程观测的巨大潜力.

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