Objective To develop a molecular biologic technique for detection of bacterial DNA in all bacteria with PCR and reverse hybridization.
目的探讨聚合酶链反应(pcr)加反相杂交技术在细菌DNA检测中的应用。
Influenza virus sample in cultured cells was treated for reverse transcription, amplification, fluorescent dye labelling, hybridization and scanning.
对待检样品进行随机逆转录和扩增，荧光标记，杂交，扫描分析。
The 16S rRNA PCR-membrane reverse dot blot hybridization technique showed that the sensitivity was 92.49%, and the specificity was 100%.
膜反向斑点杂交技术鉴定分枝杆菌菌种的灵敏度为92.49%，特异度为100%。
The 16S rRNA PCR-membrane reverse dot blot hybridization technique showed that the sensitivity was 92.49%, and the specificity was 100%.
膜反向斑点杂交技术鉴定分枝杆菌菌种的灵敏度为92.49%，特异度为100%。
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