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首页> 外文期刊>Molecular and Cellular Probes: The Location, Diagnosis and Monitoring of Disease by Specific Molecules and Cell Lines >Production of digoxigenin-labelled DNA probe for detection of Muscovy duck parvovirus.
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Production of digoxigenin-labelled DNA probe for detection of Muscovy duck parvovirus.

机译:地高辛配基标记的DNA探针的生产,用于检测番鸭细小病毒。

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摘要

A chemiluminescent dot-blot hybridization assay was developed for the detection of Muscovy duck parvovirus (DPV) by using a non-radioactive DPV DNA probe. A 1030bp HindIII-Bg/II fragment of DPV DNA was labelled with digoxigenin-labelled dUTP. The hybridized DPV DNA probes were detected by an immunoenzymatic reaction using anti-digoxigenin-antibody Fab fragments conjugated to alkaline phosphatase and visualized by chemiluminescent reaction. The assay proved to be sensitive since up to 3 fg of homologous DPV DNA and 10(0.4) EID50 mul-1 of DPV infected amino-allantoic fluid could be visualized. It appeared to be specific for the detection of different strains of DPV and Derszy's disease virus (DDV). Nevertheless, the dot-blot assay showed a lower sensitivity to detect DDV infected samples. No hybridization was noticed between DPV DNA probe and the two mammalian parvovirus strains tested (canine and porcine parvoviruses), emphasizing nucleotidic sequence heterologies. The use of the probe for DPV diagnosispurpose is discussed. To our knowledge, this work constitutes the first description of a dot-blot hybridization assay for the detection of an avian parvovirus.
机译:通过使用非放射性DPV DNA探针,开发了一种化学发光点印迹杂交测定法,用于检测番鸭细小病毒(DPV)。用洋地黄毒苷标记的dUTP标记DPV DNA的1030bp HindIII-Bg / II片段。通过使用与碱性磷酸酶偶联的抗洋地黄毒苷-抗体Fab片段的免疫酶反应,检测杂交的DPV DNA探针,并通过化学发光反应观察。该实验证明是灵敏的,因为最多可以看到3 fg的同源DPV DNA和10(0.4)EID50 mul-1 DPV感染的氨基-尿液。它似乎对检测DPV和Derszy病病毒(DDV)的不同菌株具有特异性。尽管如此,斑点印迹分析显示检测DDV感染样品的灵敏度较低。在DPV DNA探针与测试的两种哺乳动物细小病毒株(犬和猪细小病毒)之间未发现杂交,强调了核苷酸序列的异质性。讨论了探针在DPV诊断中的用途。就我们所知,这项工作构成了用于检测禽细小病毒的斑点印迹杂交测定法的第一个描述。

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