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相关概念视频

Imaging Biological Samples with Optical Microscopy01:18

Imaging Biological Samples with Optical Microscopy

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...
Phase Contrast and Differential Interference Contrast Microscopy01:26

Phase Contrast and Differential Interference Contrast Microscopy

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...
Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

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,...
Total Internal Reflection Fluorescence Microscopy01:05

Total Internal Reflection Fluorescence Microscopy

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.
Overview of Microscopy Techniques01:22

Overview of Microscopy Techniques

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...
Two-Dimensional Microscopy in Microbiology01:29

Two-Dimensional Microscopy in Microbiology

Two-dimensional (2D) microscopy encompasses a range of optical techniques that capture images within a single focal plane, offering detailed representations of microscopic structures. These techniques are essential in biological and medical research, enabling the visualization of cellular and subcellular structures with different levels of contrast and specificity.There are several major types of 2D microscopy, each with strengths and applications.Bright-Field MicroscopyBright-field microscopy...

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相关实验视频

Updated: May 8, 2026

Quantitative Optical Microscopy: Measurement of Cellular Biophysical Features with a Standard Optical Microscope
14:09

Quantitative Optical Microscopy: Measurement of Cellular Biophysical Features with a Standard Optical Microscope

Published on: April 7, 2014

单次捕捉定量斜背照明显微镜.

Paloma Casteleiro Costa1, Srinidhi Bharadwaj2,3, Zhenmin Li2

  • 1School of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, GA, USA.

Npj imaging
|March 2, 2026
PubMed
概括

单次捕获量化相位成像 (SCqOBM) 使用深度学习从一个捕获中重建3D图像. 这一进步显著加快了用于研究和诊断的生物样本的无标签成像.

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Multimodal Volumetric Retinal Imaging by Oblique Scanning Laser Ophthalmoscopy (oSLO) and Optical Coherence Tomography (OCT)
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Whole Ovary Immunofluorescence, Clearing, and Multiphoton Microscopy for Quantitative 3D Analysis of the Developing Ovarian Reserve in Mouse
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相关实验视频

Last Updated: May 8, 2026

Quantitative Optical Microscopy: Measurement of Cellular Biophysical Features with a Standard Optical Microscope
14:09

Quantitative Optical Microscopy: Measurement of Cellular Biophysical Features with a Standard Optical Microscope

Published on: April 7, 2014

Multimodal Volumetric Retinal Imaging by Oblique Scanning Laser Ophthalmoscopy (oSLO) and Optical Coherence Tomography (OCT)
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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,限制成像速度和系统简单性.

研究的目的:

  • 开发一种使用深度学习的单次捕获qOBM (SCqOBM) 方法,以实现更快,更简单的阶段恢复.
  • 在各种生物应用中验证SCqOBM的准确性和性能.

主要方法:

  • 实现了一个深度学习模型,从单个斜背照明图像进行相位重建.
  • 将SCqOBM应用于各种生物样本,包括血液流动的体内成像.
  • 评估的成像速度为单片和体积折射率断层扫描.

主要成果:

  • SCqOBM准确地重建相位信息,与传统的四捕获qOBM相似.
  • 在小鼠大脑和人手臂中证明了血液流动的非侵入性体内成像.
  • 实现了2kHz的高速定量相位成像和10卷/秒的体积断层扫描.

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.
  • 该技术适用于动态的实时应用,并为生物医学研究和诊断开辟了新的可能性.
  • SCqOBM促进了高分辨率的无标签成像,用于非侵入性血液学评估和体内组织分析.