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作 者:崔学慧[1] 陈舜胜[1] 于子翔[2] 于翠[2] 杨翠云[2]
机构地区:[1]上海海洋大学食品学院,上海201306 [2]上海出入境检验检疫局,上海200135
出 处:《上海交通大学学报(农业科学版)》2012年第5期58-63,共6页Journal of Shanghai Jiaotong University(Agricultural Science)
基 金:上海市科委技术标准专项(10DZ0503300;11dz0502700)
摘 要:以香石竹环斑病毒(Carnation ringspot virus,CRSV)的5个分离物为研究对象,分别建立了快速检测香石竹环斑病毒的多种PCR方法。结果表明,这些方法的灵敏度都比DAS-ELISA的灵敏度高,其中SYBR Green RT-PCR的灵敏度最高,可检测CRSV RNA的最低量是6.4pg。免疫磁珠RT-PCR(IMS-RT-PCR)和普通RT-PCR最低可从400ng的带毒叶片中检出CRSV,而免疫捕获RT-PCR(IC-RT-PCR)最低灵敏度可从40ng的带毒叶片中检出CRSV,是普通RT-PCR的10倍。A few of PCR methods were established for the detecting 5 isolated strains of Carnation ringspot virus (CRSV). The results showed that the sensitivities of all the PCR methods were higher than those of DAS-ELISA,and among these methods, the SYBR Green RT-PCR was most sensitive with a minimum detectable limit of 6.4 pg RNA of CRSV in sample. The minimum detectable quantity of sample for CRSV detection needed by IMS-RT-PCR and RT-PCR were 400 ng,but IC-RT-PCR only needed 40 ng of sample and the minimum sensitivity of IC-RT-PCR is the normal RT-PCR of 10 times.
关 键 词:香石竹环斑病毒 RT—PCR 免疫捕获RT—PCR免疫磁珠RT—PCR SYBR Green RT—PCR
分 类 号:S436.8[农业科学—农业昆虫与害虫防治]
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