Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Electron Microscope Tomography and Single-particle Reconstruction01:07

Electron Microscope Tomography and Single-particle Reconstruction

2.4K
Transmission electron microscopy (TEM) can be used to determine the 3D structure of biological samples with the help of techniques such as electron microscope tomography and single-particle reconstruction. While single-particle reconstruction can examine macromolecules and macromolecular complexes in vitro conditions only, tomography permits the study of cell components or small cells in vivo.
Electron Tomography
Electron tomography can be performed either in TEM or STEM (scanning transmission...
2.4K
Scanning Electron Microscopy01:07

Scanning Electron Microscopy

4.2K
A scanning electron microscope (SEM) is used to study the surface features of a sample by using an electron beam that scans the sample surface in a two-dimensional manner. Typically, areas between ~1 centimeter to 5 micrometers in width can be imaged. SEM can be used to image bacteria, viruses, tissues as well as larger samples like insects. Conventional SEM gives a magnification ranging from 20X to 30,000X and spatial resolution of 50 to 100 nanometers.
Fundamental Principles
Accelerated...
4.2K
Overview of Electron Microscopy01:25

Overview of Electron Microscopy

9.1K
The wavelengths of visible light ultimately limit the maximum theoretical resolution of images created by light microscopes. Most light microscopes can only magnify 1000X, and a few can magnify up to 1500X. Electrons, like electromagnetic radiation, can behave like waves, but with wavelengths of 0.005 nm, they produce significantly greater resolution up to 0.05 nm as compared to 500 nm for visible light. An electron microscope (EM) can create a sharp image that is magnified up to 2,000,000X.
9.1K
Transmission Electron Microscopy01:15

Transmission Electron Microscopy

5.5K
In 1931, physicist Ernst Ruska—building on the idea that magnetic fields can direct an electron beam just as lenses can direct a beam of light in an optical microscope—developed the first prototype of the electron microscope. This development led to the development of the field of electron microscopy. In the transmission electron microscope (TEM), electrons are produced by a hot tungsten element and accelerated by a potential difference in an electron gun, which gives them up to 400...
5.5K
Preparation of Samples for Electron Microscopy01:20

Preparation of Samples for Electron Microscopy

5.4K
To be visualized by an electron microscope, either transmission or scanning, biological samples need to be fixed (stabilized) so the electron beam does not destroy them and dried thoroughly (desiccated/dehydrated) so the vacuum does not affect them. Fixation needs to be done as quickly as possible because the sample properties will start changing as soon as it is removed from its natural environment. For example, in a tissue sample, the oxygen levels begin decreasing, causing an altered...
5.4K
Overview of Microscopy Techniques01:22

Overview of Microscopy Techniques

10.4K
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...
10.4K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Effect of prophylactic subcutaneous unfractionated heparin on the maternal sFlt-1/PlGF ratio: a retrospective cohort study.

BMC pregnancy and childbirth·2026
Same author

[Spontaneous resolution of ATRA-related hearing impairment without symptoms of intracranial hypertension].

[Rinsho ketsueki] The Japanese journal of clinical hematology·2026
Same author

Accelerated Discovery-to-Unveiling of High-Performance and Affordable Ammonia Electrode Process by Human-Machine Collaboration Framework.

Angewandte Chemie (International ed. in English)·2026
Same author

Mother-child correlations in hair mineral profiles in Japan: Insights from a cross-sectional study.

Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS)·2026
Same author

Atomic-scale elucidation of formation and structure in high-performance Re-Ge nanocatalysts.

Nanoscale·2026
Same author

Atomic-scale insights into the Cu ion distribution in zeolites used for ammonia selective catalytic reduction during early hydrothermal degradation.

Chemical communications (Cambridge, England)·2026
Same journal

Development of a specialized diamond knife for controlled notch introduction in ultrathin polymer films for in situ tensile transmission electron microscopy.

Microscopy (Oxford, England)·2026
Same journal

Study of nanocrystals within lamellar structures of polyvinylidene fluoride using phase plate scanning transmission electron microscopy.

Microscopy (Oxford, England)·2026
Same journal

Capability of angle-resolved SXES experiment examined by hexagonal BN and its application for the chemical bonding state of Fe2B.

Microscopy (Oxford, England)·2026
Same journal

Cryo-EELS elemental mapping of organic-solvent systems.

Microscopy (Oxford, England)·2026
Same journal

In-situ biasing DPC STEM observation of GaAs p-n junction.

Microscopy (Oxford, England)·2026
Same journal

Dynamic Scan Shaping: Overcoming Coil Hysteresis for High-Speed STEM.

Microscopy (Oxford, England)·2026
查看所有相关文章

相关实验视频

Updated: Jul 5, 2025

A Method for Obtaining Serial Ultrathin Sections of Microorganisms in Transmission Electron Microscopy
09:46

A Method for Obtaining Serial Ultrathin Sections of Microorganisms in Transmission Electron Microscopy

Published on: January 17, 2018

14.3K

使用环境和原子分辨率STEM进行深度切割.

Masaki Takeguchi1, Ayako Hashimoto1, Kazutaka Mitsuishi1

  • 1Center for Basic Research on Materials, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047, Japan.

Microscopy (Oxford, England)
|January 22, 2024
PubMed
概括
此摘要是机器生成的。

深度切割扫描传输电子显微镜 (STEM) 提高了气体或液体环境中的样品的图像分辨率. 这种技术提高了信号与背景的比率,使环境细胞能够进行原子级成像.

关键词:
在3D中,它是3D.深度切割 切割的深度这是一个声音.原子分辨率的原子分辨率我们的环境环境环境环境环境环境环境.气体 气体 气体 气体这是一种液态液体液体.

更多相关视频

Array Tomography Workflow for the Targeted Acquisition of Volume Information using Scanning Electron Microscopy
09:47

Array Tomography Workflow for the Targeted Acquisition of Volume Information using Scanning Electron Microscopy

Published on: July 15, 2021

4.8K
Three-dimensional Characterization of Interorganelle Contact Sites in Hepatocytes using Serial Section Electron Microscopy
09:12

Three-dimensional Characterization of Interorganelle Contact Sites in Hepatocytes using Serial Section Electron Microscopy

Published on: June 9, 2022

5.7K

相关实验视频

Last Updated: Jul 5, 2025

A Method for Obtaining Serial Ultrathin Sections of Microorganisms in Transmission Electron Microscopy
09:46

A Method for Obtaining Serial Ultrathin Sections of Microorganisms in Transmission Electron Microscopy

Published on: January 17, 2018

14.3K
Array Tomography Workflow for the Targeted Acquisition of Volume Information using Scanning Electron Microscopy
09:47

Array Tomography Workflow for the Targeted Acquisition of Volume Information using Scanning Electron Microscopy

Published on: July 15, 2021

4.8K
Three-dimensional Characterization of Interorganelle Contact Sites in Hepatocytes using Serial Section Electron Microscopy
09:12

Three-dimensional Characterization of Interorganelle Contact Sites in Hepatocytes using Serial Section Electron Microscopy

Published on: June 9, 2022

5.7K

科学领域:

  • 材料科学 材料科学 材料科学
  • 显微镜的使用方法
  • 纳米技术 纳米技术

背景情况:

  • 环境电池 (EC) 传输电子显微镜 (TEM) 可使用化膜对气体和液体介质中的样品进行成像.
  • 在EC-TEM中实现高分辨率受到信号与背景比率的挑战.
  • 深度切割扫描TEM (STEM) 提供了一种方法来增强矩阵内样本的信号.

研究的目的:

  • 引入深度切割STEM作为高分辨率成像技术.
  • 审查环境细胞中深度切割STEM的应用.
  • 突出气体和液体环境中原子级分辨率的潜力.

主要方法:

  • 使用深度截面扫描TEM (STEM) 原则.
  • 采用带有化膜的环境电池 (EC) 来进行样本封装.
  • 在各种介质上获取扫描传输电子显微镜 (TEM) 图像.

主要成果:

  • 深度切割STEM可以提高样品的信号与背景比.
  • 该技术允许提高分辨率,可能达到原子水平.
  • 在气体和液体介质内成像样本的成功应用.

结论:

  • 深度切割STEM是一种强大的技术,用于高分辨率的环境传输电子显微镜.
  • 它克服了EC-TEM中信号与背景比率所带来的分辨率限制.
  • 能够在研究原始气态或液态的材料和工艺方面进行先进的应用.