Search research articles

相关概念视频

Super-resolution Fluorescence Microscopy

Super-resolution Fluorescence Microscopy

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...

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

Local mitochondrial physiology defined by mtDNA quality guides purifying selection.

PLoS genetics·2026

Same author

Nanoscale dynamics of enhancer-promoter interactions during exit from pluripotency.

Nucleic acids research·2025

Same author

Generation of densely labeled oligonucleotides for the detection of small genomic elements.

Cell reports methods·2024

Same author

Nucleosome spacing controls chromatin spatial structure and accessibility.

Biophysical journal·2024

Same author

Regulatory evolution tuning pigmentation intensity quantitatively in <i>Drosophila</i>.

Science advances·2024

Same author

Rapid and synchronous chemical induction of replicative-like senescence via a small molecule inhibitor.

Aging cell·2024

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 Journal Methods Collections JoVE Encyclopedia of Experiments 存档

教育

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual 教师资源中心教师网站

使用条款与条件

Search research articles

相关实验视频

Updated: Jan 13, 2026

Visualization of the Immunological Synapse by Dual Color Time-gated Stimulated Emission Depletion STED Nanoscopy

Visualization of the Immunological Synapse by Dual Color Time-gated Stimulated Emission Depletion STED Nanoscopy

Published on: March 24, 2014

一个灵活的框架,用于自动化STED超分辨率显微镜.

¹Computational BioImaging, Faculty of Biology, LMU Munich, Munich, Germany. hoerl@bio.lmu.de.

Scientific reports

|January 9, 2026

概括

使用autoSTED软件的自动成像管道加快了超分辨率显微镜的速度. 这种框架使细胞结构的动态,适应性成像成为可能,减少了研究人员的偏见和实践时间.

科学领域:

细胞和分子成像技术
生物物理学的生物物理.
显微镜技术显微镜技术

背景情况:

超分辨率显微镜提供了高细节,但受到高光暴露和缓慢成像速度的影响.
当前的方法往往只对选定的地区进行成像,限制了公正的人口研究.
自动化的飞行区域检测对于高效的超高分辨率成像至关重要.

研究的目的:

为了介绍autoSTED,一个Python框架用于在STIMulated Emission Depletion (STED) 显微镜中自动化成像管道.
为了实现超越固定采集循环的动态和适应性成像策略.
为了促进计算机视觉方法的集成,用于增强显微镜工作流程.

主要方法:

开发自动STED,这是一个灵活的Python框架,用于获取任务的优先级队列.
实现回调函数用于基于获取数据的动态任务生成.
模块化设计允许轻松交换构建块和自定义代码集成.

主要成果:

自动STED可以构建用于STED显微镜的自动成像管道.
该框架支持动态和自适应成像,超越静态采集协议.
已经证明有潜力显著加速亚细胞结构的超高分辨率成像.

更多相关视频

A Guide to Structured Illumination TIRF Microscopy at High Speed with Multiple Colors

A Guide to Structured Illumination TIRF Microscopy at High Speed with Multiple Colors

Published on: May 30, 2016

Super-Resolution Microscopy of the Synaptonemal Complex Within the Caenorhabditis elegans Germline

Super-Resolution Microscopy of the Synaptonemal Complex Within the Caenorhabditis elegans Germline

Published on: September 13, 2022

相关实验视频

Last Updated: Jan 13, 2026

Visualization of the Immunological Synapse by Dual Color Time-gated Stimulated Emission Depletion STED Nanoscopy

Visualization of the Immunological Synapse by Dual Color Time-gated Stimulated Emission Depletion STED Nanoscopy

Published on: March 24, 2014

A Guide to Structured Illumination TIRF Microscopy at High Speed with Multiple Colors

A Guide to Structured Illumination TIRF Microscopy at High Speed with Multiple Colors

Published on: May 30, 2016

Super-Resolution Microscopy of the Synaptonemal Complex Within the Caenorhabditis elegans Germline

Super-Resolution Microscopy of the Synaptonemal Complex Within the Caenorhabditis elegans Germline

Published on: September 13, 2022

结论:

自动STED极大地加快了亚细胞结构的超高分辨率成像.
该框架允许自主显微镜操作,最小偏差和实践时间.
通过autoSTED,可以在大型细胞群中对细胞特征进行无偏见的定量分析.