A nonradioactive dot-blot hybridization for Epstain-Barr virus with probe generated using the polymerase chain reaction

Yali Chen , Zuhong Lu , Weiping Wang , Mei Zhou , Jianguo Wu
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Abstract

A nonradioactive probe was utilized in dot-blot hybridization for the detection of infectious Epstein-Barr virus. A polymerase chain reaction PCR-generated oligonucleotide, a 121 bp segment was labeled with digoxigenin (DIG)-11-dUTP. The hybridization results were detected by using an alkaline phosphatase-conjugated antibody to DIG and the enzyme substrates. The DIG-EB DNA allowed the detection limit in 0.1 pg of DNA. The samples from fifteen patients with nasopharyneal cancer (NPC) were examined.

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用聚合酶链反应产生探针对eb病毒进行非放射性斑点杂交
采用非放射性探针进行斑点杂交检测感染性eb病毒。聚合酶链反应聚合酶链反应生成的寡核苷酸,121 bp的片段用地高辛(DIG)-11-dUTP标记。用碱性磷酸酶偶联抗体检测DIG和酶底物的杂交结果。digi - eb DNA的检出限为0.1 pg。本文对15例鼻咽癌(NPC)患者的标本进行了检查。
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Editorial Publisher's note A nonradioactive dot-blot hybridization for Epstain-Barr virus with probe generated using the polymerase chain reaction A novel amphiphilic push-pull ferrocene derivative: Langmuir–Blodgett films and second-order optical nonlinearity Interaction of poly-L-lysine with photosynthetic reaction center for the Langmuir–Blodgett film preparation
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