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Preliminary Study on Detecting the SARS-CoV Specific Target cDNA Fragments by Multiplex PCR

机译:多重PCR检测SARS-CoV特异靶cDNA片段的初步研究

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The multiplex polymerase chain reaction (PCR) technique was applied to detect the SARS-CoV (severe acute respiratory syndrome-associated coronavirus) specific target cDNA fragments in the present study. The target cDNA fragments of SARS-CoV were synthesized artificially according to the genome sequence of SARS-CoV in GenBank submitted by The Chinese University of Hong Kong, and were used as simulated positive samples. Five primers recommended by World Health Organization (WHO) were used to amplify the fragments by single PCR and multiplex PCR. Three target cDNA fragments (121, 182 and 302 bp), as well as the three different combinations of any two of these fragments, were amplified by single PCR. The combination of these three fragments was amplified by multiplex PCR. The results indicated that the multiplex PCR technique could be applied to detect the SARS-CoV specific target cDNA fragments successfully.
机译:在本研究中,采用了多重聚合酶链反应(PCR)技术来检测SARS-CoV(严重急性呼吸综合征相关冠状病毒)特异性靶cDNA片段。根据香港中文大学提交的GenBank中SARS-CoV的基因组序列,人工合成SARS-CoV的靶cDNA片段,并将其用作模拟阳性样品。使用世界卫生组织(WHO)推荐的五种引物通过单次PCR和多重PCR扩增片段。通过一次PCR扩增了三个靶cDNA片段(121、182和302 bp)以及这些片段中任意两个的三种不同组合。通过多重PCR扩增这三个片段的组合。结果表明,多重PCR技术可以成功地检测SARS-CoV特异性靶cDNA片段。

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