1) virulent duck plague virus
鸭瘟强毒
1.
The propagation characteristics of virulent duck plague virus(DPV)in duck embryo fibroblast(DEF)were studied by the method of light microscopy observation of DEF cell culture monolayer,electron microscopy observation of infected DEF cell culture,real-time PCR detecting virus propagation.
通过细胞培养物光学显微观察、细胞超薄切片研究、定量PCR检测技术对鸭胚成纤维细胞中鸭瘟强毒的增殖特性进行了研究。
2) duck plague virus virulent strain
鸭瘟病毒强毒
1.
Replication kinetics of duck plague virus virulent strain in parenchymatous organs of experimentally infected ducklings;
鸭瘟病毒强毒株在感染鸭实质器官内的增殖与分布
3) Attenuated and Virulent DPV
鸭瘟弱毒及强毒株
4) duck plague virus
鸭瘟病毒
1.
Dynamics of IFN-α mRNA expression in liver of ducks infected with duck plague virus of different virulence;
鸭瘟病毒疫苗株与强毒株诱导雏鸭IFN-α mRNA在肝脏中表达的动态定量研究
2.
Purification and electron microscopy observation after negative staining of duck plague virus;
鸭瘟病毒的纯化及电镜负染形态观察
3.
Prokaryotic expression of N-terminal antigenic domain of duck plague virus gB protein and the establishment of putative indirect ELISA assay;
鸭瘟病毒gB蛋白N端主要抗原域的表达及间接ELISA检测
5) DPV
鸭瘟病毒
1.
The SD-01 strain of DPV was propagated in chicken embryo fibroblast monolayer cells.
将鸭瘟病毒分离株SD-01在鸡胚成纤维细胞上增殖。
2.
According to the UL6 and UL7 gene data of duck plague virus(DPV),a pair of primers were designed and used for a polymerase chain reaction(PCR) with two duck plague vaccine strains and one standard strain and one field isolate.
根据鸭瘟病毒UL6和UL7基因序列,设计合成了一对引物,以2株疫苗株1、株强毒株和1株山东分离株DNA为模板,进行PCR扩增,得到预期690 bp的目的片段。
3.
According to DPV gC gene sequence discovered by our laboratory,a series of scientific research were conducted and the results were obtained as followed: 1.
本文对本实验室发现的鸭瘟病毒gC基因开展系列研究,获如下结果: 1。
6) duck plague attenuated vaccine virus
鸭瘟弱毒株
补充资料：强毒
【强毒】
（术语）强结毒鼓之缘之意。又作疆毒。谓于无大善根者，强说法华经而使之谤，以结逆缘也。法华文句所谓“本已有善，释迦以小而将护之，本未有善，不轻以大而强毒之”是也。
（术语）强结毒鼓之缘之意。又作疆毒。谓于无大善根者，强说法华经而使之谤，以结逆缘也。法华文句所谓“本已有善，释迦以小而将护之，本未有善，不轻以大而强毒之”是也。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条