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目的 建立适用于牡蛎和粪便中快速、特异、灵敏的GⅠ、GⅡ型诺如病毒(NV)定量分型诊断方法.方法 通过对GⅠ、GⅡ型NV基因组保守序列的比对分析,设计高度特异的引物和探针,建立以TaMan探针为基础的实时聚合酶链反应方法(TaMan Real-time RT-PCR).结果 该方法对NV核酸检测高度特异,且GⅠ和GⅡ型之间无交叉反应,最低检出限达102 copies/μl.对90份新鲜牡蛎样品和37份腹泻粪便标本分别用常规RT-PCR和笔者建立的TaMan Real-time RT-PCR进行NV检测,发现牡蛎样品中后者的检出率明显高于前者,而粪便标本中两者无明显差别.同时对阳性标本的测序分析证实结果准确可靠.结论 研究中建立的TaMan Real-time RT-PCR方法可用于海产品标本及粪便中NV定量及分型检测,可作为应对NV胃肠炎暴发的有效诊断方法. 相似文献
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《Science & Sports》2002,17(5):263-265
Introduction – Finswimming is a new sport activity. The optimization of the leg’s propulsive action is fundamental to improve the performance. The aim of this work is to quantify finswimmer’s movements per race distances, using a kinematic analysis.Fact synthesis – Five elite finswimmers were video recorded during underwater races. The connections between the average velocity of stroke, frequency and range of finswimmers undulation are observed as a fonction of race distance.Conclusion – Finswimmers are shown to adjust and to stabilize instantaneously their movements in terms of race distance. 相似文献
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