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相关概念视频

PCR01:32

PCR

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Overview
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Real Time RT-PCR02:57

Real Time RT-PCR

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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...
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RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

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Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific...
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The Replisome03:01

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DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or the replisome.
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with...
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Lagging Strand Synthesis01:59

Lagging Strand Synthesis

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During replication, the complementary strands in double-stranded DNA are synthesized at different rates. Replication first begins on the leading strand. Replication starts later, occurs more slowly, and proceeds discontinuously on the lagging strand.
There are several major differences between synthesis of the leading strand and synthesis of the lagging strand. 1) Leading strand synthesis happens in the direction of replication fork opening, whereas lagging strand synthesis happens in the...
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Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

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Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
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相关实验视频

Updated: Jul 18, 2025

Linear Amplification Mediated PCR – Localization of Genetic Elements and Characterization of Unknown Flanking DNA
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Linear Amplification Mediated PCR – Localization of Genetic Elements and Characterization of Unknown Flanking DNA

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长距离聚合酶连锁反应

Ping Siu Kee1, Harsheni Karunanathie2, Simran D S Maggo1,3

  • 1Department of Pathology and Biomedical Science, University of Otago, Christchurch, New Zealand.

Methods in molecular biology (Clifton, N.J.)
|August 22, 2023
PubMed
概括

远程聚合酶连锁反应 (PCR) 成功地放大了高达20kB的大型DNA片段. PCR增强剂对于放大困难的DNA点至关重要,提高长距离PCR效率.

关键词:
阿加罗斯凝电泳DNA聚合酶是一种DNA聚合酶.长的安普利康斯长的安普利康斯.长距离聚合酶连锁反应 (PCR)在PCR添加剂中使用PCR添加剂.增强PCR的增强剂是PCR增强剂.药物遗传学 药物遗传学设计初级设计 设计初级设计校对酶检查检查检查检查检查检查检查检查热循环是一个热循环.

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相关实验视频

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Linear Amplification Mediated PCR – Localization of Genetic Elements and Characterization of Unknown Flanking DNA
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Linear Amplification Mediated PCR – Localization of Genetic Elements and Characterization of Unknown Flanking DNA

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Associated Chromosome Trap for Identifying Long-range DNA Interactions

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科学领域:

  • 分子生物学分子生物学
  • 遗传学 是一个遗传学.

背景情况:

  • 聚合酶链反应 (PCR) 是用于DNA放大的一种标准实验室技术.
  • 远程PCR是一种专门的方法,旨在放大广泛的DNA片段.

研究的目的:

  • 适应和优化一个远程PCR协议,用于放大人类基因组DNA的大型DNA片段.
  • 评估PCR增强剂在提高远程PCR成功率方面的有效性.

主要方法:

  • 使用了一种适应的远程PCR协议.
  • 来自人类基因组DNA的不同大小 (6.6,7.2,13,和20kb) 的增强DNA片段.
  • 评估了PCR增强剂对放大成功的影响.

主要成果:

  • 成功生成了从6.6kb到20kb的PCR产品.
  • 证明PCR增强剂对于某些长DNA片段的成功放大是必要的.
  • 提供了关于特定增强剂在远程PCR中的有效性数据.

结论:

  • 适应的远程PCR协议对于放大大DNA片段是有效的.
  • PCR增强剂显著提高了远程PCR的成功和效率,特别是在具有挑战性的目标上.