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相关概念视频

Leaky Scanning02:28

Leaky Scanning

5.1K
During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R...
5.1K
Real Time RT-PCR02:57

Real Time RT-PCR

56.9K
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...
56.9K
Initiation of Translation02:33

Initiation of Translation

31.2K
Initiating translation is complex because it involves multiple molecules. Initiator tRNA, ribosomal subunits, and eukaryotic initiation factors (eIFs) are all required to assemble on the initiation codon of mRNA. This process consists of several steps that are mediated by different eIFs.
First, the initiator tRNA must be selected from the pool of elongator tRNAs by eukaryotic initiation factor 2 (eIF2). The initiator tRNA (Met-tRNAi) has conserved sequence elements including modified bases at...
31.2K
Ribosome Profiling02:24

Ribosome Profiling

3.5K
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...
3.5K

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相关实验视频

Updated: Jun 7, 2025

Aptamer-Based Target Detection Facilitated by a 3-Stage G-Quadruplex Isothermal Exponential Amplification Reaction
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Aptamer-Based Target Detection Facilitated by a 3-Stage G-Quadruplex Isothermal Exponential Amplification Reaction

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分裂探针诱导的蛋白质转化放大用于核酸检测.

Yoo-Hong Min1,2, Yoonseo Hong1, Cheol-Hee Kim2

  • 1Critical Diseases Diagnostics Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 34141, Republic of Korea.

ACS applied bio materials
|November 15, 2024
PubMed
概括

这项研究介绍了一种新型的分裂探头传感器,用于高度敏感和准确的核酸检测. 该方法增强了在生物样本中检测微RNA的信号生成.

关键词:
没有细胞的蛋白质合成.外基因组是外基因组中的一个.这是一个小RNARNA.纳米光线的使用方法核酸检测核酸检测检测sfGFPFP 的价格为分裂探测器探测器 分裂探测器

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Measurement of Specific Mycobacterial Mistranslation Rates with Gain-of-function Reporter Systems
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Measurement of Specific Mycobacterial Mistranslation Rates with Gain-of-function Reporter Systems

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Quantitative Immunofluorescence to Measure Global Localized Translation
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Quantitative Immunofluorescence to Measure Global Localized Translation

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相关实验视频

Last Updated: Jun 7, 2025

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Measurement of Specific Mycobacterial Mistranslation Rates with Gain-of-function Reporter Systems
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科学领域:

  • 生物化学 生物化学
  • 分子生物学分子生物学
  • 生物技术是生物技术.

背景情况:

  • 核酸检测对于诊断,研究和法医非常重要.
  • 当前的方法往往缺乏灵敏度,准确性或负担能力.
  • 敏感和特定的核酸检测是一个持续的挑战.

研究的目的:

  • 开发一种简单,灵敏和准确的核酸检测方法.
  • 通过分探针策略和体外翻译放大来提高灵敏度.
  • 为了使多个微RNA (miRNA) 的同时检测.

主要方法:

  • 使用分探针策略与记者蛋白的体内翻译放大相结合.
  • 设计了一种光分裂探针传感器,采用具有明显光波长的记者蛋白.
  • 通过修改记者蛋白序列以提高灵敏度来进行内置的发光检测.

主要成果:

  • 在检测目标microRNAs (miRNAs) 中实现了高灵敏度和选择性.
  • 从细胞系和细胞外囊泡中成功分析和量化miRNAs.
  • 该系统能够使用多种光记者同时检测多个miRNA.

结论:

  • 开发的分裂探头传感器为核酸检测提供了一个简单,灵敏和特定的工具.
  • 这种方法对包括诊断和研究在内的各种应用具有重大潜力.
  • 该系统的适应性允许检测各种向核酸.