Cloning and mapping of BamHi endonuclease fragments of DNA from the transforming B95-8 strain of Epstein-Barr virus.
Cloning and mapping of BamHi endonuclease fragments of DNA from the transforming B95-8 strain of Epstein-Barr virus.
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对 Epstein-Barr 病毒 B95-8 转化株 DNA 的 BamHi 核酸内切酶片段进行克隆和定位。
DOI：
10.1073/pnas.77.7.3860
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发表时间：
1980
影响因子：
11.1
通讯作者：
Strominger,JL
中科院分区：
文献类型：
--
作者：
Skare,J;Strominger,JL
用BamHI内切核酸酶（EC 3.1.23.6）将来自EB病毒B 95 -8株的DNA切割成29个不同的片段。除末端片段外的所有片段都已插入pBR 322克隆载体中并在大肠杆菌中复制。每个克隆的DNA片段在病毒基因组中的位置已经确定，提供了比以前更详细的基因组物理图谱。
DNA from the B95-8 strain of Epstein-Barr virus was cleaved into 29 different fragments by BamHI endonuclease (EC 3.1.23.6). All of the fragments except the terminal fragments have been inserted into the pBR322 cloning vector and replicated in Escherichia coli. The location of each cloned DNA fragment in the viral genome has been determined, providing a more detailed physical map of the genome than has been available previously.