摘要
将O、A型FMDVRNA分离纯化,用RT-PCR法扩增其聚合酶编码基因,可检测到A型10-6倍稀释、O型10-4倍稀释乳鼠肌肉毒。Nested-PCR扩增该基因内部片段,进一步说明该方法准确可靠。RT-PCR一步完成使整个检测时间不超过12小时。
An RT PCR was developed to amplify the RNAs of Types A and O FMDV.The sensitivity reached 10 -6 for Type A and 10 -4 for Type O.Amplification of the inner fragments of the gene confirmed the reliabilty for the detection of FMDV.The completion of the whole RT PCR was no more than 12 hours .It is suggested that RT PCR be applied for the import quarantine diagnosis and detection of FMD.
出处
《中国动物检疫》
CAS
1997年第2期3-5,共3页
China Animal Health Inspection