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采用原位杂交技术检测爱泼斯坦-巴尔病毒(EBV)DNA序列。

Detection of Epstein-Barr virus (EBV) DNA sequences using in situ hybridization.

作者信息

Moar M H, Klein G

出版信息

Biochim Biophys Acta. 1978 Jun 22;519(1):49-64. doi: 10.1016/0005-2787(78)90061-8.

Abstract

In situ hybridization was used to detect Epstein-Barr virus (EBV) DNA sequences under conditions where the virus DNA is replicating spontaneously and where it is induced to do so following superinfection. The in situ reaction itself is influenced by several parameters, analogous to conventional nucleic acid hybridization, consideration of which should help to optimize the designing of in situ hybridization reactions in general. Both EBV complementary RNA (cRNA) and EBV DNA synthesized in vitro can efficiently detect the virus DNA sequences in situ. The findings presented here can therefore be utilized in both the study of EBV-cell interactions and, more generally, in studies using in situ hybridization as a general approach.

摘要

原位杂交用于在病毒DNA自发复制以及超感染后诱导其复制的条件下检测爱泼斯坦-巴尔病毒(EBV)DNA序列。原位反应本身受几个参数的影响,这与传统核酸杂交类似,考虑这些参数应有助于总体上优化原位杂交反应的设计。体外合成的EBV互补RNA(cRNA)和EBV DNA均可有效原位检测病毒DNA序列。因此,本文呈现的研究结果可用于EBV与细胞相互作用的研究,更广泛地讲,也可用于将原位杂交作为通用方法的研究。

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