猪细小病毒DNA的分子克隆,以期在细菌中合成病毒抗原。

A D Zaberezhny, A L Konorova
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引用次数: 0

摘要

在Pr-lambda和lac-启动子控制下,在大肠杆菌中获得了猪细小病毒1.05 kb DNA片段的表达。在pr控制下表达的产物显示出ppv特异性抗原特性。其电泳迁移率对应的分子量约为45 KD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular cloning of porcine parvovirus DNA for the purpose of obtaining viral antigen synthesis in bacteria.

An expression of porcine parvovirus 1.05 kb DNA fragment was obtained in Escherichia coli under the control both of Pr-lambda and lac-promoters. The product of expression under Pr-control was demonstrated to show PPV-specific antigenic properties. Its electrophoretic mobility corresponded to a molecular weight of approximately 45 KD.

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