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

Flow Cytometry01:23

Flow Cytometry

14.2K
The development of flow cytometry techniques began in 1934 with initial attempts by Andrew Moldavan, a bacteriologist who counted the cells in a flowing capillary system. Moldavan pumped cells through a capillary tube focused under a microscope for visualization. The invention of photometry allowed the measurement of differentially-stained cells, and Louis Kamentsky developed the first multiparameter flow cytometer in 1965 to identify and count the cancer cells in cervical tissue specimens.
In...
14.2K

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

Modular training resources for bioimage analysis.

Journal of microscopy·2026
Same author

Targeted single-cell RNA and perturbation sequencing with TAP-seq.

Nature protocols·2026
Same author

GloBIAS: strengthening the foundations of bioimage analysis.

Nature methods·2026
Same author

Genome-scale mapping of variant, enhancer and gene function in primary human CD4+ T cells.

bioRxiv : the preprint server for biology·2026
Same author

Ki-67 shapes the nucleolus by anchoring chromatin via its amphiphilic properties.

The EMBO journal·2026
Same author

Harnessing lipid-driven immunometabolic pathways in omental metastases to enhance immunotherapy in patients with ovarian cancer.

Signal transduction and targeted therapy·2026
Same journal

A native sulfur deposit in Gale crater, Mars.

Science (New York, N.Y.)·2026
Same journal

Coordinated demise of harmful algal blooms.

Science (New York, N.Y.)·2026
Same journal

Genetic effects put into context.

Science (New York, N.Y.)·2026
Same journal

Bacteria share proteins to survive antibiotics.

Science (New York, N.Y.)·2026
Same journal

Impacts shaped Earth's first continents.

Science (New York, N.Y.)·2026
Same journal

Erratum for the Report "Covalently bonded single-molecule junctions with stable and reversible photoswitched conductivity" by C. Jia <i>et al</i>.

Science (New York, N.Y.)·2026
查看所有相关文章

相关实验视频

Updated: Oct 6, 2025

Immunophenotyping and Cell Sorting of Human MKs from Human Primary Sources or Differentiated In Vitro from Hematopoietic Progenitors
14:30

Immunophenotyping and Cell Sorting of Human MKs from Human Primary Sources or Differentiated In Vitro from Hematopoietic Progenitors

Published on: August 7, 2021

7.0K

高速光图像支持的细胞分类

Daniel Schraivogel1, Terra M Kuhn2, Benedikt Rauscher1

  • 1Genome Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.

Science (New York, N.Y.)
|January 20, 2022
PubMed
概括
此摘要是机器生成的。

高速图像启用细胞分类 (ICS) 精确地根据形态和蛋白质定位隔离单个细胞. 这种先进的细胞分类技术加速了全基因组选,并扩大了表型分析能力.

更多相关视频

Fluorescence Activated Cell Sorting of Plant Protoplasts
13:35

Fluorescence Activated Cell Sorting of Plant Protoplasts

Published on: February 18, 2010

25.1K
Purification of Specific Cell Population by Fluorescence Activated Cell Sorting FACS
15:29

Purification of Specific Cell Population by Fluorescence Activated Cell Sorting FACS

Published on: July 10, 2010

74.1K

相关实验视频

Last Updated: Oct 6, 2025

Immunophenotyping and Cell Sorting of Human MKs from Human Primary Sources or Differentiated In Vitro from Hematopoietic Progenitors
14:30

Immunophenotyping and Cell Sorting of Human MKs from Human Primary Sources or Differentiated In Vitro from Hematopoietic Progenitors

Published on: August 7, 2021

7.0K
Fluorescence Activated Cell Sorting of Plant Protoplasts
13:35

Fluorescence Activated Cell Sorting of Plant Protoplasts

Published on: February 18, 2010

25.1K
Purification of Specific Cell Population by Fluorescence Activated Cell Sorting FACS
15:29

Purification of Specific Cell Population by Fluorescence Activated Cell Sorting FACS

Published on: July 10, 2010

74.1K

科学领域:

  • 细胞生物学
  • 生物技术
  • 基因组学

背景情况:

  • 隔离具有特定空间和形态特征的单个细胞是一个重要的技术障碍.
  • 目前的细胞分类方法缺乏捕获复杂细胞表型的分辨率.

研究的目的:

  • 为精确的单细胞隔离开发一个高速图像支持的细胞分类 (ICS) 方法.
  • 通过先进的表型分析扩大细胞分类和聚合遗传查的能力.

主要方法:

  • 已建立能够记录多色光图像和分类细胞的高速图像分类系统 (ICS).
  • 使用ICS来量化细胞形态,蛋白质定位和线性阶段,以增强细胞周期分析.
  • 结合ICS和CRISPR组合查以快速进行全基因组查.

主要成果:

  • ICS成功量化了细胞形态和蛋白质定位,提高了细胞周期分析的分辨率.
  • 在大约9小时内完成全基因组图像屏幕.
  • 证明了核因子KB (NF-KB) 路径调节者的鉴定.

结论:

  • ICS显著扩大了细胞分类和聚合基因选的表型空间.
  • 这项技术为分析复杂的细胞表型和加速生物发现提供了强大的工具.