A plasmid vector for cloning directly at the transcription initiation site of a bacteriophage T7 promoter.
作者信息
Petty I T
机构信息
Department of Plant Pathology, University of California, Berkeley 94720.
出版信息
Nucleic Acids Res. 1988 Sep 12;16(17):8738. doi: 10.1093/nar/16.17.8738.
Abstract
摘要
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本文引用的文献
1
Production of single-stranded plasmid DNA.单链质粒DNA的制备。
Methods Enzymol. 1987;153:3-11. doi: 10.1016/0076-6879(87)53044-0.
2
Studies on SP6 promoter using a new plasmid vector that allows gene insertion at the transcription initiation site.使用一种新型质粒载体对SP6启动子进行研究，该载体允许在转录起始位点插入基因。
Nucleic Acids Res. 1987 Mar 11;15(5):2279-94. doi: 10.1093/nar/15.5.2279.
3
DNA inserted two bases down from the initiation site of a SP6 polymerase transcription vector is transcribed efficiently in vitro.插入到SP6聚合酶转录载体起始位点下游两个碱基处的DNA在体外能被高效转录。
Nucleic Acids Res. 1987 Feb 11;15(3):1337. doi: 10.1093/nar/15.3.1337.
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