Cloning and analysis of PCR-generated DNA fragments.

G L Costa, A Grafsky, M P Weiner
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引用次数: 31

Abstract

Methods are presented for the improved yield and analysis of blunt-ended cloning of PCR-generated DNA fragments. We show that Pfu DNA polymerase polishing of Taq DNA polymerase-generated fragments increases the yield and efficiency of cloning. Using a triple primer set consisting of two outside, asymmetrically distanced primers and one fragment-specific primer, both the presence and orientation of cloned inserts can be determined. Application of these methods allows the generation and cloning of a fragment in 1 day and the analysis of putative clones the next, thereby saving a substantial amount of both time and effort.

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pcr生成DNA片段的克隆与分析。
提出了提高产量和分析pcr产生的DNA片段钝端克隆的方法。我们发现Pfu DNA聚合酶对Taq DNA聚合酶产生的片段进行抛光可以提高克隆的产量和效率。使用由两个外部非对称距离引物和一个片段特异性引物组成的三重引物,可以确定克隆插入物的存在和方向。应用这些方法可以在1天内生成和克隆一个片段,并在第二天分析假定的克隆,从而节省了大量的时间和精力。
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Rapid and sensitive analysis of mRNA polyadenylation states by PCR. Identification of 3'-terminal exons from yeast artificial chromosomes. Quantitative analysis of specific mRNA transcripts using a competitive PCR assay with electrochemiluminescent detection. Batched analysis of genotypes. A one-step coupled amplification and oligonucleotide ligation procedure for multiplex genetic typing.
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