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

Protein Dynamics in Living Cells01:19

Protein Dynamics in Living Cells

2.7K
Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
2.7K
Overview Of Cell Separation And Isolation01:20

Overview Of Cell Separation And Isolation

7.6K
Cell separation was first achieved in 1964 by S. H. Seal, who separated large tumor cells from the smaller blood cells using filtration. Two years later, Pohl and Hawk performed experiments on how cells respond differently to a nonuniform electric field based on the cell type. Such observations were the inception of cell separation methods, which allow isolating a single cell type from a heterogeneous sample.
7.6K
Matrix-Assisted Laser Desorption Ionization (MALDI)01:08

Matrix-Assisted Laser Desorption Ionization (MALDI)

1.2K
Matrix-assisted laser desorption ionization (MALDI) is a powerful analytical technique used in mass spectrometry. It enables the identification and characterization of various biomolecules, including proteins, peptides, nucleic acids, and carbohydrates. MALDI is an ionization technique, widely employed in biological and medical research, as well as in fields like pharmacology and biochemistry.The analyte of interest, a biomolecule or a mixture of biomolecules, is mixed with a suitable matrix...
1.2K
DNA Isolation01:34

DNA Isolation

199.5K
DNA from cells is required for many biotechnology and research applications, such as molecular cloning. To remove and purify DNA from cells, researchers use various methods of DNA extraction. While the specifics of different protocols may vary, some general concepts underlie the process of DNA extraction.
199.5K
DNA Isolation01:24

DNA Isolation

45.1K
DNA isolation protocols can be fast and straightforward or complex and time-consuming depending on the type and quality of DNA required for further processing. For example, plasmid DNA extraction is a bit more complicated than genomic DNA extraction because of the need for an appropriate lysis method to separate plasmid DNA from gDNA during isolation. However, for specific applications, such as long-range DNA sequencing that require a good yield of high- quality DNA samples, we need to follow...
45.1K
Chemistry of the Cell02:58

Chemistry of the Cell

48.0K
The cell is chemically composed of water, organic molecules and inorganic ions.
Water
The polarity of the water molecule and its resulting hydrogen bonding makes water a unique substance with special properties that are intimately tied to the processes of life. Life originally evolved in an aqueous environment, and most of an organism’s cellular chemistry and metabolism occur inside the aqueous contents of the cell’s cytoplasm. Special properties of water are its high heat capacity...
48.0K

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

In vivo chemogenetic generation of intraneuronal H<sub>2</sub>O<sub>2</sub>.

Free radical biology & medicine·2026
Same author

Fiber-optic platform for infrared laser thermogenetic stimulation and multimodal optical readout in freely moving animals.

Optics express·2025
Same author

Epilepsy Treatment through Genetic Intervention of GABAergic Interneurons: Promises and Challenges.

ACS chemical neuroscience·2025
Same author

The Endoplasmic Reticulum-Located TRPV1 Channel Is Not Thermal Sensitive.

ACS chemical biology·2025
Same author

Human TRPV1 is an efficient thermogenetic actuator for chronic neuromodulation.

Cellular and molecular life sciences : CMLS·2024
Same author

Identification of De Novo Dividing Stem Cells.

Methods in molecular biology (Clifton, N.J.)·2024

相关实验视频

Updated: Feb 4, 2026

Laser Capture Microdissection of Mammalian Tissue
16:34

Laser Capture Microdissection of Mammalian Tissue

Published on: October 1, 2007

17.5K

通过激光捕捉微解剖来隔离活细胞.

Ekaterina A Elesina1,2, Ulyana V Khlebnikova1,2, Oleg V Podgorny1,3,4

  • 1Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, Russia.

Methods in molecular biology (Clifton, N.J.)
|February 2, 2026
PubMed
概括

活细胞激光微解剖能够精确地将单细胞和细胞群从培养物中分离出来. 这种方法保留了细胞完整性,用于下游分子分析和再培养.

关键词:
细胞培养培养的细胞培养.细胞分离 细胞分离隔离活细胞的隔离.激光微切割是指激光微切割.再种植是为了重新培养.

更多相关视频

Laser Capture Microdissection of Drosophila Peripheral Neurons
12:02

Laser Capture Microdissection of Drosophila Peripheral Neurons

Published on: May 24, 2010

14.0K
Laser Capture Microdissection of Neurons from Differentiated Human Neuroprogenitor Cells in Culture
12:38

Laser Capture Microdissection of Neurons from Differentiated Human Neuroprogenitor Cells in Culture

Published on: September 16, 2013

12.6K

相关实验视频

Last Updated: Feb 4, 2026

Laser Capture Microdissection of Mammalian Tissue
16:34

Laser Capture Microdissection of Mammalian Tissue

Published on: October 1, 2007

17.5K
Laser Capture Microdissection of Drosophila Peripheral Neurons
12:02

Laser Capture Microdissection of Drosophila Peripheral Neurons

Published on: May 24, 2010

14.0K
Laser Capture Microdissection of Neurons from Differentiated Human Neuroprogenitor Cells in Culture
12:38

Laser Capture Microdissection of Neurons from Differentiated Human Neuroprogenitor Cells in Culture

Published on: September 16, 2013

12.6K

科学领域:

  • 细胞生物学 细胞生物学
  • 分子生物学分子生物学
  • 生物技术是生物技术.

背景情况:

  • 精确的分子分析需要纯粹和均的细胞样本.
  • 现有的细胞隔离方法往往会分离细胞,影响下游分析.
  • 活细胞隔离对于奥米克研究和再培养至关重要.

研究的目的:

  • 通过激光微解剖来提出一种新的活细胞隔离协议.
  • 为了使单细胞和细胞碎片在不脱离基质的情况下收集.
  • 为了促进下游的分子分析和完整细胞的再培养.

主要方法:

  • 活细胞激光微解剖 (LCLM) 技术.
  • 重力转移用于收集孤立的细胞.
  • 在附着细胞培养物上应用.

主要成果:

  • 单细胞和细胞群的成功隔离.
  • 细胞完整性和完整状态的保存.
  • 对于下游的奥米克分析和回收培养的可行性已被证明.

结论:

  • 活细胞激光微解剖与重力转移是获得纯细胞种群的有效方法.
  • 这种技术克服了传统细胞隔离方法的局限性.
  • 它支持先进的分子分析和细胞再培养应用.