Efficient cloning of fragments of the polymerase chain reaction directly into the single stranded bacteriophage M13mp18.
作者信息
Zimmer W
机构信息
Botanisches Institut, Universität zu Köln, Germany.
出版信息
Nucleic Acids Res. 1993 Feb 11;21(3):773-4. doi: 10.1093/nar/21.3.773.
Abstract
摘要
相似文献
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Efficient cloning of fragments of the polymerase chain reaction directly into the single stranded bacteriophage M13mp18.将聚合酶链反应片段高效直接克隆到单链噬菌体M13mp18中。
Nucleic Acids Res. 1993 Feb 11;21(3):773-4. doi: 10.1093/nar/21.3.773.
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本文引用的文献
1
New M13 vectors for cloning.用于克隆的新型M13载体。
Methods Enzymol. 1983;101:20-78. doi: 10.1016/0076-6879(83)01005-8.
2
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.
3
Lambda ZAP: a bacteriophage lambda expression vector with in vivo excision properties.λZAP：一种具有体内切除特性的λ噬菌体表达载体。
Nucleic Acids Res. 1988 Aug 11;16(15):7583-600. doi: 10.1093/nar/16.15.7583.
4
Using the polymerase chain reaction to modify expression plasmids for epitope mapping.利用聚合酶链反应修饰表达质粒用于表位作图。
Nucleic Acids Res. 1989 Apr 25;17(8):3319. doi: 10.1093/nar/17.8.3319.
5
Novel non-templated nucleotide addition reactions catalyzed by procaryotic and eucaryotic DNA polymerases.原核生物和真核生物DNA聚合酶催化的新型非模板核苷酸添加反应。
Nucleic Acids Res. 1988 Oct 25;16(20):9677-86. doi: 10.1093/nar/16.20.9677.
6
Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products.T载体的构建，一种用于直接克隆未修饰PCR产物的快速通用系统。
Nucleic Acids Res. 1991 Mar 11;19(5):1154. doi: 10.1093/nar/19.5.1154.
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