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

Fluorescence and Phosphorescence: Instrumentation01:25

Fluorescence and Phosphorescence: Instrumentation

561
Fluorometers and spectrofluorometers are two types of instruments used for measuring molecular fluorescence. These instruments differ in how they select excitation and emission wavelengths and the type of light sources they utilize. Fluorometers use absorption interference filters to choose excitation and emission wavelengths. The excitation source in a fluorometer is typically a low-pressure mercury vapor lamp that emits intense lines distributed throughout the ultraviolet and visible regions.
561
Total Internal Reflection Fluorescence Microscopy01:05

Total Internal Reflection Fluorescence Microscopy

5.7K
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.
5.7K
Photoluminescence: Applications01:14

Photoluminescence: Applications

385
Photoluminescence offers a wide range of applications due to its inherent sensitivity and selectivity. This technique allows for both direct and indirect analyses of the analyte. Direct quantitative analysis is possible when the analyte exhibits a favorable quantum yield for fluorescence or phosphorescence. However, an indirect analysis may be feasible if the analyte is not fluorescent or phosphorescent, or if the quantum yield is unfavorable. Indirect methods include reacting the analyte with...
385
Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

6.9K
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...
6.9K
Atomic Spectroscopy: Absorption, Emission, and Fluorescence01:23

Atomic Spectroscopy: Absorption, Emission, and Fluorescence

841
Atomic spectroscopy is a vital tool in elemental analysis, both qualitatively and quantitatively. It can be broadly divided into optical spectroscopy, mass spectroscopy, and X-ray spectroscopy methods. The optical spectroscopic methods are atomic absorption spectroscopy (AAS), atomic emission spectroscopy (AES), and atomic fluorescence spectroscopy (AFS). The first step in all three methods is atomization, where the solid, liquid, or solution-phase samples are converted into gas-phase atoms and...
841

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

Upper-state-assisted uphill energy transfer in a far-red light-harvesting antenna from an Antarctic alga.

The Journal of chemical physics·2026
Same author

Spectroscopic Characterization of the Charge-Separated Zwitterionic State Responsible for the Excimer-like Emission of a Luminescent Diradical.

Journal of the American Chemical Society·2025
Same author

Localization of the Au-Au bond strength in the triplet excited state of the [Au(CN)<sub>2</sub> <sup>-</sup>] oligomers revealed by ultrafast time-domain Raman spectroscopy.

Chemical science·2025
Same author

Dynamic Excited-State Localization Induced by Jahn-Teller Distortion Observed by Coherent Vibrational Spectroscopy.

Journal of the American Chemical Society·2025
Same author

Ultrafast Protein Dynamics Prior to Retinal Photoisomerization in Microbial Rhodopsins.

The journal of physical chemistry letters·2025
Same author

Excited-State Aromatization Drives Nonequilibrium Planarization Dynamics.

Journal of the American Chemical Society·2025

相关实验视频

Updated: Jun 17, 2025

Dual-Color Fluorescence Cross-Correlation Spectroscopy to Study Protein-Protein Interaction and Protein Dynamics in Live Cells
14:12

Dual-Color Fluorescence Cross-Correlation Spectroscopy to Study Protein-Protein Interaction and Protein Dynamics in Live Cells

Published on: December 11, 2021

5.2K

室温溶液光激发相关性谱学

Yusuke Yoneda1,2, Hikaru Kuramochi1,2

  • 1Research Center of Integrative Molecular Systems (CIMoS), Institute for Molecular Science, National Institutes of Natural Sciences, 38 Nishigo-Naka, Myodaiji, Okazaki 444-8585, Japan.

The journal of physical chemistry letters
|August 12, 2024
PubMed
概括

这项研究引入了光激发相关性光谱学,以观察室温溶液中的快速分子光谱变化. 这种新方法实现了微秒分辨率,使得动态分子过程的研究成为可能.

科学领域:

  • 物理化学 物理化学
  • 频谱学是一种光谱学.
  • 单分子生物物理学 单分子生物物理学

背景情况:

  • 单分子光谱对于研究分子性质至关重要.
  • 在室温下调查溶液中自由扩散的分子的快速动态是具有挑战性的.

研究的目的:

  • 开发一种方法来研究单个分子水平的室温溶液中激发光谱的快波动力学.
  • 为了使微秒时间分辨率的自发光谱变化的调查.

主要方法:

  • 使用光激发相关性光谱学.
  • 采用宽带五分秒脉冲的里埃变换光谱学.
  • 应用时间相关的单光子计数用于单分子测量.

主要成果:

  • 在室温溶液中实现了单分子光激发光谱.
  • 获得的激发波长解析的光自相关函数在微秒到毫秒范围内.
  • 证明了该方法在研究依赖时间的激发光谱变化方面的潜力.

结论:

  • 开发的方法允许在统计学上平衡的系统中研究快速,自发的激发频谱波动.
  • 进一步的发展可以使得光谱交换的研究具有前所未有的时间分辨率.

更多相关视频

A Fluorescence Fluctuation Spectroscopy Assay of Protein-Protein Interactions at Cell-Cell Contacts
08:43

A Fluorescence Fluctuation Spectroscopy Assay of Protein-Protein Interactions at Cell-Cell Contacts

Published on: December 1, 2018

11.3K
High Precision FRET at Single-molecule Level for Biomolecule Structure Determination
11:24

High Precision FRET at Single-molecule Level for Biomolecule Structure Determination

Published on: May 13, 2017

10.7K

相关实验视频

Last Updated: Jun 17, 2025

Dual-Color Fluorescence Cross-Correlation Spectroscopy to Study Protein-Protein Interaction and Protein Dynamics in Live Cells
14:12

Dual-Color Fluorescence Cross-Correlation Spectroscopy to Study Protein-Protein Interaction and Protein Dynamics in Live Cells

Published on: December 11, 2021

5.2K
A Fluorescence Fluctuation Spectroscopy Assay of Protein-Protein Interactions at Cell-Cell Contacts
08:43

A Fluorescence Fluctuation Spectroscopy Assay of Protein-Protein Interactions at Cell-Cell Contacts

Published on: December 1, 2018

11.3K
High Precision FRET at Single-molecule Level for Biomolecule Structure Determination
11:24

High Precision FRET at Single-molecule Level for Biomolecule Structure Determination

Published on: May 13, 2017

10.7K
  • 这种技术为溶液中的分子动力学提供了新的见解.