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Confocal Fluorescence Microscopy01:16

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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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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.
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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...
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Total internal reflection fluorescence microscopy or TIRF is an advanced microscopic technique used to visualize fluorophores in samples close to a solid surface with a higher refractive index, such as a glass coverslip. TIRF only allows fluorophores in proximity to the solid surface to be excited. When light from a medium with a lower refractive index (such as air) hits the glass coverslip at a critical angle, the light undergoes total internal reflection stead of passing through the glass.
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Updated: Sep 12, 2025

Whole Ovary Immunofluorescence, Clearing, and Multiphoton Microscopy for Quantitative 3D Analysis of the Developing Ovarian Reserve in Mouse
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单次捕捉量化斜背照明显微镜

Paloma Casteleiro Costa, Srinidhi Bharadwaj, Zhenmin Li

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    此摘要是机器生成的。

    单次捕获定量斜背照明显微镜 (SCqOBM) 使用深度学习进行快速,无标签的3D相位成像. 这种先进的技术实现了高精度,通过简化硬件实现实时生物可视化.

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    科学领域:

    • 生物医学光学 生物医学光学
    • 显微镜的使用方法
    • 计算成像技术的成像

    背景情况:

    • 定量斜背照明显微镜 (qOBM) 能够对厚厚的生物样本进行无标签的3D相位成像.
    • 传统的qOBM需要多次捕获,限制成像速度并增加系统复杂性.

    研究的目的:

    • 引入使用深度学习进行快速相位恢复的单次捕获qOBM (SCqOBM).
    • 为了证明SCqOBM在体内和高速成像应用中的准确性和潜力.

    主要方法:

    • 从单个斜背照明图像进行相位重建的深度学习模型的开发.
    • 使用多种生物标本对SCqOBM与传统的四捕获qOBM进行验证.
    • SCqOBM的应用用于血液流动的体内成像和高速断层成像.

    主要成果:

    • SCqOBM从单次捕获中准确地重建相位信息,与传统的qOBM结果相匹配.
    • 在小鼠大脑和人类手臂中,证明了血液流动的非侵入性可视化.
    • 实现了2kHz的单片定量相位成像和10卷/秒的体积折射率断层扫描.

    结论:

    • SCqOBM显著提高了成像速度,并简化了定量相位成像的硬件要求.
    • 该技术为动态的实时生物医学研究和临床诊断提供了变革性的优势.
    • SCqOBM促进了高分辨率,无标签的3D成像,为体内组织分析和血液学评估开辟了新的途径.