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相关概念视频

RNA-seq03:21

RNA-seq

11.7K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
11.7K
Nonsense-mediated mRNA Decay02:27

Nonsense-mediated mRNA Decay

11.7K
The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
11.7K
RNA Stability01:53

RNA Stability

35.6K
Intact DNA strands can be found in fossils, while scientists sometimes struggle to keep RNA intact under laboratory conditions. The structural variations between RNA and DNA underlie the differences in their stability and longevity. Because DNA is double-stranded, it is inherently more stable. The single-stranded structure of RNA is less stable but also more flexible and can form weak internal bonds. Additionally, most RNAs in the cell are relatively short, while DNA can be up to 250 million...
35.6K
Real Time RT-PCR02:57

Real Time RT-PCR

64.6K
Real-time reverse transcription-polymerase chain reaction, or Real-time RT-PCR, is an analytical tool used to determine the expression level of target genes. The method involves converting mRNA to complementary DNA with the help of an enzyme known as reverse transcriptase, followed by the PCR amplification of the cDNA. These two processes can be performed simultaneously in a single tube or separately as a two-step reaction.
The real-time quantification of the number of amplified products is...
64.6K
Ribosome Profiling02:24

Ribosome Profiling

4.1K
Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
4.1K
Nuclear Export of mRNA02:31

Nuclear Export of mRNA

8.7K
Before mRNAs are exported to the cytoplasm, it is crucial to check each mRNA for structural and functional integrity. Eukaryotic cells use several different mechanisms, collectively known as mRNA surveillance, to look for irregularities in mRNAs. Irregular or aberrant mRNA are rapidly degraded by various enzymes. If a defective mRNA escapes the surveillance, it would be translated into a protein which would either be non-functional or not function properly. One of the primary irregularities in...
8.7K

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相关实验视频

Updated: Jan 14, 2026

Metabolic Labeling of Newly Transcribed RNA for High Resolution Gene Expression Profiling of RNA Synthesis, Processing and Decay in Cell Culture
11:00

Metabolic Labeling of Newly Transcribed RNA for High Resolution Gene Expression Profiling of RNA Synthesis, Processing and Decay in Cell Culture

Published on: August 8, 2013

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通过单分子纳米孔传感量化RNA降解.

Max K Earle1, Mohammed Alawami1, Raluca-Elena Alexii1

  • 1Cavendish Laboratory, University of Cambridge, JJ Thomson Avenue, Cambridge CB3 0HE, U.K.

Analytical chemistry
|October 23, 2025
PubMed
概括

固态纳米孔传感为RNA降解分析提供了一种敏感的方法,只需要100ppg的RNA. 这种技术克服了凝电泳对低丰度或高分子量RNA样本的局限性.

科学领域:

  • 生物化学 生物化学
  • 分子生物学分子生物学
  • 纳米技术 纳米技术

背景情况:

  • RNA的化学不稳定性在诊断和治疗方面带来了挑战.
  • 凝电泳是RNA降解评估的标准,但需要大量的RNA数量 (≥100 ng).
  • 需要敏感的方法来分析像mRNA疫苗和病毒RNA这样有价值的样本中的RNA降解.

研究的目的:

  • 引入和评估固态纳米孔传感用于评估RNA降解.
  • 为了证明该方法对低丰度RNA样本的灵敏度和适用性.
  • 为了比较纳米孔传感与传统的凝电泳,用于RNA完整性分析.

主要方法:

  • 利用固态纳米孔传感用于单分子分辨率分析RNA降解.
  • 在广泛的RNA度范围内测试了该方法的性能.
  • 在各种实验条件下评估病毒RNA降解.

主要成果:

  • 纳米孔感应成功评估了单分子分辨率的病毒RNA降解.
  • 与凝电泳相比,这种方法在显著较低的RNA量 (仅为100 pg) 时是有效的.
  • 已证明用于分析RNA样本的实用性,不适合基于凝的方法,因为其度低或分子量高.

更多相关视频

Measurement of mRNA Decay Rates in Saccharomyces cerevisiae Using rpb1-1 Strains
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Measurement of mRNA Decay Rates in Saccharomyces cerevisiae Using rpb1-1 Strains

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Determining Genome-wide Transcript Decay Rates in Proliferating and Quiescent Human Fibroblasts
07:03

Determining Genome-wide Transcript Decay Rates in Proliferating and Quiescent Human Fibroblasts

Published on: January 2, 2018

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相关实验视频

Last Updated: Jan 14, 2026

Metabolic Labeling of Newly Transcribed RNA for High Resolution Gene Expression Profiling of RNA Synthesis, Processing and Decay in Cell Culture
11:00

Metabolic Labeling of Newly Transcribed RNA for High Resolution Gene Expression Profiling of RNA Synthesis, Processing and Decay in Cell Culture

Published on: August 8, 2013

27.7K
Measurement of mRNA Decay Rates in Saccharomyces cerevisiae Using rpb1-1 Strains
12:21

Measurement of mRNA Decay Rates in Saccharomyces cerevisiae Using rpb1-1 Strains

Published on: December 13, 2014

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Determining Genome-wide Transcript Decay Rates in Proliferating and Quiescent Human Fibroblasts
07:03

Determining Genome-wide Transcript Decay Rates in Proliferating and Quiescent Human Fibroblasts

Published on: January 2, 2018

6.6K

结论:

  • 固态纳米孔传感为评估RNA完整性提供了高度敏感和定量方法.
  • 这种方法扩大了RNA样本的分析能力,特别是那些数量有限或分子量高的样本.
  • 纳米孔传感在各种研究和临床应用中代表了RNA分析的宝贵进步.