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prv

  • 网络减压阀;伪狂犬病病毒;伪狂犬病毒;猪伪狂犬病病毒;猪伪狂犬病毒
prvprv
  1. Previous studies have demonstrated PRV infection triggered efficient immune response .

    以前的研究表明,PRV感染能有效诱导机体天然免疫。

  2. By the above experiment results , the isolated virus was identified as PRV .

    通过上述试验结果证明,该分离毒株为伪狂犬病毒。

  3. Comprehensive measures were taken on 5 PRV infected farms with satisfactory results achieved .

    我们对5个PRV污染的猪场采取了综合控制措施,取得了较好的效果。

  4. Prokaryotic Expression of PRV gE Gene and Establishment of Indirect ELISA

    伪狂犬病病毒gE基因的原核表达及间接ELISA方法的建立

  5. Studies on the detection of PRV antibody using Dot-PPA-ELISA in pig serum

    Dot-PPA-ELISA检测猪血清伪狂犬病抗体的研究

  6. Study on Functions of PRV Major Virulent Genes

    伪狂犬病病毒主要毒力基因功能的研究

  7. Biological Characteristics of Pseudorabies Virus ( PRV ) Vaccine Strain

    伪狂犬病毒弱毒株若干生物学特性

  8. The study on safety and immunity of PRV oil emulsion inactivated vaccine to piglets

    伪狂犬病油乳剂灭活苗对新生仔猪的安全性和免疫原性研究

  9. Discussion on the hydraulic calculation of inlet / discharge piping to / from PRV

    安全阀进出口管道水力学计算若干问题探讨

  10. Cloning and Probe Preparation of the Specific Glycoprotein gp 50 of PRV

    PRV特异性糖蛋白gp50基因片段的克隆探针制备

  11. Ultrastructure of the PRV gene-deleted strains in cell proliferation in vitro

    PRV基因缺失株在体外细胞中增殖的超微结构

  12. Three questions about the hydraulic calculation of inlet / discharge piping to / from PRV are discussed .

    针对安全阀进出口管道水力学计算中常遇到的3个问题进行了讨论。

  13. We utilized recombinant antigen and developed an indirect ELISA assay for detecting PRV antibodies .

    本研究应用重组抗原,成功建立了检测猪伪狂犬病病毒血清抗体的间接ELISA诊断方法。

  14. The Construction and Expression of PRV PK / gG / GFP Recombinant Transfer Vector

    伪狂犬病毒PK/gG/GFP重组转移载体的构建和表达

  15. We could conclude that MMLS broad antimicrobial spectrum and good inhibiting effects on PRV .

    MMLS具有广谱的抑菌作用和抗伪狂犬病毒作用。

  16. Operator assembly Pack PRV in wrong way ( opposed right to left ), How to avoid this issue ?

    操作员汇编组装PRV用错误方式(被反对的右到左),如何避免这个问题?

  17. Pressure Relief Valve ( PRV ) is one of the most important and the most frequently-used components in industrial production .

    减压阀是工业生产中常用和重要的稳压元器件之一。

  18. Cloning , Sequencing and a Highly Repeated and Altered Region Analysis of gD Gene of PRV LA Strain

    PRVLA株gD基因的序列测定及其重复高变区的发现

  19. Cloning , Sequencing and Structural Evolution Analysis of the Thymidine Kinase Gene of a Wild Chinese PRV LA Strain

    猪伪狂犬病毒鲁A株TK基因的序列测定及其结构功能与进化分析渤海湾地区中西部中生代构造特征及演化

  20. In pig production , A group PRV virus is one of the main cause and virulence pathogens of diarrhoea .

    在养猪生产上,A组PRV是引起幼猪腹泻的主要病毒性病原体之一。

  21. Then four different gene deletional vaccines of PRV were detected by the multi-PCR .

    利用建立的Multi-PCR方法,对商品化的四种不同基因缺失的PRV疫苗进行检测,其扩增结果与疫苗的基因缺失背景一致。

  22. Altogether , these results suggest that a distinct pathway utilized by PRV to regulate innate immunity .

    这些结果提示PRV通过一种独特的机制调节天然免疫。

  23. Virus neutralization ( VN ) test showed that the isolate could be neutralized by PRV positive serum .

    细胞中和试验表明,该病毒能被猪伪狂犬病病毒标准阳性血清所中和。

  24. TK gene is the main virulent gene , TK deletion may remarkably lower or loss PRV virulence ;

    TK基因是主要毒力基因,其缺失引起PRV毒力丧失或极显著地降低;

  25. Studies on dynamic regularity of antibody after immunization of cows and goats with different assistant PRV inactive vaccines

    不同佐剂PRV灭活苗免疫奶牛及山羊抗体消长规律研究

  26. Prokaryotic Expression of Porcine PRV gD and gE Genes and Development of Monoclonal Antibodies against PRV

    猪伪狂犬病毒gD和gE基因的原核表达及单克隆抗体的研制

  27. Study on the homology between PRV FB low virulent strain and gE and gI of PA strain

    PRVFB弱毒株与FA株gE,gI基因的同源性研究

  28. The recurrent mechanism of PRV latency reactivation determines the persistence of virus in swine herd .

    这种伪狂犬病病毒潜伏-激活循环机制决定了伪狂犬病病毒在猪群中的永远存在。

  29. The research also has a great significance in exploration of molecular epidemiology of PRV and the development of diagnosis and prophylaxis against PRV .

    该研究从血清学、病原学和分子生物学方面证实新疆存在PRV野毒株,对于新疆PRV的流行病学研究及诊断和防治具有重要意义。

  30. This recombinant virus strain can be used for the study of duel-valence vaccine of JEV and PRV .

    该重组病毒可作为猪乙脑和伪狂犬病双价基因工程疫苗用毒株。