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

Recombinant DNA01:09

Recombinant DNA

Overview
Labeling DNA Probes03:31

Labeling DNA Probes

DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
DNA Microarrays02:34

DNA Microarrays

Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
Heterochromatin02:38

Heterochromatin

The extent of chromatin compaction can be studied by staining chromatin using specific DNA binding dyes. Under the microscope, the dense-compacted regions that take up more dye are called heterochromatin. Heterochromatin is further classified into two forms – constitutive heterochromatin and facultative heterochromatin.
Constitutive heterochromatin: It is a highly compact region of chromatin that is mostly concentrated in the centromere and telomere. Unlike euchromatin, the amino acid at 9th...
Single-Strand DNA Binding Proteins01:03

Single-Strand DNA Binding Proteins

For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...

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

Phosphorothioate-Free and Self-Interaction-Reduced Acyclic Nucleic Acids for Effective Antisense Oligonucleotide.

Journal of medicinal chemistry·2026
Same author

An acyclic nucleic acid-modified siRNA targeting CAG expansions for polyglutamine disease treatment.

Molecular therapy. Nucleic acids·2026
Same author

Membrane-Penetrating Molecular Device Based on a Triplex Containing Acyclic L-Threoninol Nucleic Acid Functionalized with Cholesterol.

Angewandte Chemie (International ed. in English)·2025
Same author

Staple oligomers induce a stable RNA G-quadruplex structure for protein translation inhibition in therapeutics.

Nature biomedical engineering·2025
Same author

Reversible photocycloaddition of 8-pyrenylvinylguanine for photoreactive serinol nucleic acid (SNA).

Organic & biomolecular chemistry·2025
Same author

Highly Effective Chemical Ligation of DNA and l-aTNA.

Current protocols·2025

相关实验视频

Updated: Jun 25, 2026

Combining QD-FRET and Microfluidics to Monitor DNA Nanocomplex Self-Assembly in Real-Time
14:36

Combining QD-FRET and Microfluidics to Monitor DNA Nanocomplex Self-Assembly in Real-Time

Published on: August 26, 2009

用于可控制的H聚合的DNA染料合物(1)

Hiroyuki Asanuma1, Kenji Shirasuka, Tohru Takarada

  • 1Research Center for Advanced Science and Technology, The University of Tokyo, Komaba, Meguro-ku, Tokyo 153-8904, Japan. asanuma@mkomi.rcast.u-tokyo.ac.jp

Journal of the American Chemical Society
|February 20, 2003
PubMed
概括

研究人员合成了DNA-甲基红联物,形成了H聚合物. 这些DNA染料聚合物的光谱特性随着DNA双重组的形成而可逆地发生变化,证明了对聚合结构的控制.

科学领域:

  • 超分子化学 超分子化学
  • 生物物理化学 生物物理化学
  • 材料科学 材料科学 材料科学

背景情况:

  • 基于DNA的纳米材料具有独特的结构性质.
  • 控制DNA支架内的染料聚合对于功能应用至关重要.
  • 甲基红色染料可以形成具有明显光谱特征的H聚合物.

研究的目的:

  • 在DNA结合物中合成和表征甲基红H聚合物.
  • 研究DNA结构对H聚合物形成和光谱特性的影响.
  • 通过DNA杂交证明H聚合物结构的可逆控制.

主要方法:

  • 合成与多个甲基红色部分结合的DNA结合物.
  • 紫外线-紫外线光谱学用于监测光谱变化.
  • 热变性化研究 (T(m)) 来评估DNA双重组的形成.

主要成果:

  • 成功合成了DNA-甲基红结合物,形成了H聚合物.
  • 观察到显著的低染色度和带收窄随着染料的增加,表明H聚合物形成.
  • 在DNA双重组形成和解离时,证明了可逆光谱变化 (H波段的消失和重新出现).

更多相关视频

Synthesis of Wavelength-shifting DNA Hybridization Probes by Using Photostable Cyanine Dyes
07:44

Synthesis of Wavelength-shifting DNA Hybridization Probes by Using Photostable Cyanine Dyes

Published on: July 6, 2016

DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation
09:26

DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation

Published on: December 29, 2021

相关实验视频

Last Updated: Jun 25, 2026

Combining QD-FRET and Microfluidics to Monitor DNA Nanocomplex Self-Assembly in Real-Time
14:36

Combining QD-FRET and Microfluidics to Monitor DNA Nanocomplex Self-Assembly in Real-Time

Published on: August 26, 2009

Synthesis of Wavelength-shifting DNA Hybridization Probes by Using Photostable Cyanine Dyes
07:44

Synthesis of Wavelength-shifting DNA Hybridization Probes by Using Photostable Cyanine Dyes

Published on: July 6, 2016

DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation
09:26

DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation

Published on: December 29, 2021

结论:

  • DNA-甲基红合物可以形成明确的H聚合物.
  • 这些聚合物的光谱特性对DNA结构变化敏感.
  • DNA杂交提供了一种可逆的机制来控制甲基红H聚合物的形成和结构.