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A Colony Multiplex Quantitative PCR-Based 3S3DBC Method and Variations of It for Screening DNA Libraries.

机译:基于菌落多重定量PCR的3S3DBC方法及其变体,用于筛选DNA库。

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摘要

A DNA library is a collection of DNA fragments cloned into vectors and stored individually in host cells, and is a valuable resource for molecular cloning, gene physical mapping, and genome sequencing projects. To take the best advantage of a DNA library, a good screening method is needed. After describing pooling strategies and issues that should be considered in DNA library screening, here we report an efficient colony multiplex quantitative PCR-based 3-step, 3-dimension, and binary-code (3S3DBC) method we used to screen genes from a planarian genomic DNA fosmid library. This method requires only 3 rounds of PCR reactions and only around 6 hours to distinguish one or more desired clones from a large DNA library. According to the particular situations in different research labs, this method can be further modified and simplified to suit their requirements.
机译:DNA库是克隆到载体中的DNA片段的集合,并分别存储在宿主细胞中,是分子克隆,基因物理作图和基因组测序项目的宝贵资源。为了充分利用DNA文库的优势,需要一种良好的筛选方法。在描述了合并策略和DNA文库筛选中应考虑的问题后,我们在此报告了一种有效的基于菌落多重定量PCR的3步,3维和二进制代码(3S3DBC)方法,用于从涡虫中筛选基因基因组DNA fosmid文库。该方法仅需3轮PCR反应,仅需约6小时即可从大型DNA文库中区分出一个或多个所需克隆。根据不同研究实验室的具体情况,可以进一步修改和简化此方法,以适应他们的要求。

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