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相关概念视频

Labeling DNA Probes03:31

Labeling DNA Probes

8.4K
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...
8.4K
FISH - Fluorescent In-situ Hybridization02:07

FISH - Fluorescent In-situ Hybridization

21.3K
Fluorescence in situ hybridization, or FISH, was developed in the early 1980s and has quickly become one of the most widely used techniques in cytogenetics. Labeled probes are used to bind complementary DNA or RNA sequences on a chromosome or in a region within a cell. Earlier, the probes could only be obtained by cloning or reverse transcription of a DNA template. Currently, the probe oligonucleotides can be synthesized synthetically. Additionally, with the advancement of optical techniques,...
21.3K
In-situ Hybridization02:31

In-situ Hybridization

9.6K
In situ hybridization (ISH) is a technique used to detect and localize specific DNA or RNA molecules in cells, tissue, or tissue sections using a labeled probe. The technique was first used in 1969 for the investigation of nucleic acids. It is currently an essential tool in scientific research and clinical settings, especially for diagnostic purposes.
Types of probes and labels
A probe is a complementary strand of DNA or RNA that binds to corresponding nucleotide sequences in a cell. Many...
9.6K
Southern Blot02:57

Southern Blot

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Agarose gel electrophoresis is very useful in separating DNA fragments by size. Running a DNA ladder containing fragments of the known length alongside the sample helps determine the approximate length of the sample DNA fragments. However, additional steps are needed to verify the sequence identity of the sample DNA fragments.
Denatured DNA fragments must be transferred onto a carrier membrane from the gel to make it accessible to a probe - a small ssDNA fragment complementary to the target DNA...
20.2K
DNA Microarrays02:34

DNA Microarrays

18.5K
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...
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相关实验视频

Updated: Sep 13, 2025

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

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分裂杂交探测器使用DNA光照明Aptamer作为序列特定核酸分析的信号报告器.

AnnaMarie Knowles1, Justine Monsalve1, Yulia Gerasimova2

  • 1Chemistry Department, University of Central Florida.

Journal of visualized experiments : JoVE
|July 28, 2025
PubMed
概括

基于DNA的光照明光体 (FLAP) 提供了一种无标签,低成本的方法来检测核酸点. 这项研究详细介绍了一种用于分光升级阿帕特马传感器 (SLAS) 的算法,使得单核酸替代分析具有精确性.

科学领域:

  • 生物化学 生物化学
  • 分子生物学分子生物学
  • 分析化学 分析化学

背景情况:

  • 传统的核酸检测通常需要标记的探头,增加成本和复杂性.
  • 光照明吸光体 (FLAP) 提供了一个无标签的替代品,利用在结合时光的染料连接体.
  • 据报道,DAP-10-42是最有效的DNA FLAP,显示了生物传感的巨大潜力.

研究的目的:

  • 描述基于高效的DNA FLAP,DAP-10-42.的分光光吸纳体传感器 (SLAS) 设计的算法.
  • 为了实现序列特定的核酸检测与单核酸分辨率的应用程序,如单核酸替代 (SNS) 分析.
  • 突出SLAS在各种生物传感环境中无标签,基于光检测的优势.

主要方法:

  • 开发一种算法来设计分光升级吸收器传感器 (SLAS).
  • 使用DAP-10-42 DNA FLAP作为传感器构建的核心组件.
  • 配备SLAS配备了对特定结合的目标核酸的补充序列.

主要成果:

  • 通过SLAS,可以对特定序列的核酸目标进行特定的检测.
  • 开发的传感器实现了高选择性,直到单核酸分辨率,用于SNS分析.
  • 光信号的读数是无标签的,并且与标准的度仪和视觉观测相兼容.

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Single-Cell Multiplexed Fluorescence Imaging to Visualize Viral Nucleic Acids and Proteins and Monitor HIV, HTLV, HBV, HCV, Zika Virus, and Influenza Infection
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Simple Method for Fluorescence DNA In Situ Hybridization to Squashed Chromosomes
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Simple Method for Fluorescence DNA In Situ Hybridization to Squashed Chromosomes

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相关实验视频

Last Updated: Sep 13, 2025

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

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Single-Cell Multiplexed Fluorescence Imaging to Visualize Viral Nucleic Acids and Proteins and Monitor HIV, HTLV, HBV, HCV, Zika Virus, and Influenza Infection
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Single-Cell Multiplexed Fluorescence Imaging to Visualize Viral Nucleic Acids and Proteins and Monitor HIV, HTLV, HBV, HCV, Zika Virus, and Influenza Infection

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Simple Method for Fluorescence DNA In Situ Hybridization to Squashed Chromosomes
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Simple Method for Fluorescence DNA In Situ Hybridization to Squashed Chromosomes

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结论:

  • SLAS方法为核酸分析提供了一个多功能和高效的平台.
  • SLAS提供了一种无标签,低成本和敏感的方法来检测核酸点,包括单核酸变异.
  • 这项技术有望用于疾病诊断,环境监测和生物分子研究等领域.