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gpv

  • 网络鹅细小病毒;小鹅瘟病毒;鹅副粘病毒;山羊痘病毒;绿激光汽化术
gpvgpv
  1. Establishment and Application of the PCR Assay for Detection of GPV

    鹅细小病毒PCR检测方法的建立及应用

  2. Cloning and Sequence Analysis of the partial genome of GPV and MPV and Expression of VP 2 - VP 3 Gene

    鹅细小病毒和番鸭细小病毒部分基因组克隆、序列分析及VP2-VP3基因的表达

  3. The study provided a technology platform for further study on GPV live vector vaccine and related foundation research .

    本实验为进一步开展GTPV活载体疫苗的研制及相关基础研究提供了技术平台。

  4. Identification & Pathogenic Test on a GPV Wild Strain

    GPV野毒株鉴定及其致病力试验

  5. Isolation of GPV wild strain and detection by PCR

    GPV野毒株的分离及PCR检测方法的应用

  6. Purification and serological studies on the GPV strain of wheat yellow dwarf virus

    小麦黄矮病毒GPV株系的提纯及血清学研究

  7. Transgenic Wheat Resistant to Barley Yellow Dwarf Virus GPV Using Replicase Gene

    大麦黄矮病毒GPV株系复制酶基因介导的抗病毒转基因小麦的研究

  8. Objective To study the security , reliability of GPV in the treatment of with glandular cystitis .

    目的研究绿激光治疗腺性膀胱炎的安全性和可靠性。

  9. Conclusion It is secure and efficient to treat glandular cystitis with GPV .

    结论绿激光治疗腺性膀胱炎,是一种安全有效的微创疗法。

  10. Construction of Recombinant Fowlpox Virus Transfer Vector and DNA Vaccine of GPV and GPMV

    GPV与GPMV重组禽痘病毒转移载体和DNA疫苗的构建

  11. Western blot and IFA showed that the four McAbs could combine with the natural GPV .

    westernblot及间接免疫荧光显示,4株单抗均能与天然GPV结合。

  12. Development of McAb to GPV and the Study on ICS to Diagnose GPV

    小鹅瘟病毒单克隆抗体的制备及胶体金诊断试纸的研究

  13. Dot-ELISA Method for Detecting GPV Infected Antibody

    检测小鹅瘟感染抗体的Dot-ELISA方法研究

  14. This study established a foundation for the industrialization of the PPRV recombinant GPV vaccine .

    本研究为小反刍兽疫重组山羊痘疫苗的产业化提供了参考。

  15. We have purified the samples of GPV strain , and improved and simplified the procedure of purification .

    并对GPV株系毒源进行了提纯;对其提纯方法有所改进和简化。

  16. GPV can be regarded as a mark reflecting the degree of platelet activation in AMI patients .

    GPV可以作为反映冠心病患者病程中血小板活化程度的一项新指标。

  17. RAPD marker of resistance gene to strain GPV of BYDV in wheat addition line Z1

    抗大麦黄矮病毒GPV株系小麦异附加系Z1抗性基因的RAPD标记

  18. Dynamic Distribution of Virulent GPV in Vivo and Molecular Analysis on Structure of the Intestinal Flora after Infected GPV

    小鹅瘟强毒在人工感染雏鹅体内侵染规律及对消化道菌群结构影响的分子解析

  19. Development of Indirect in Situ PCR for the Detection of GPV and Study GPV Infection Law in Goslings Experimental Infected

    间接原位PCR检测GPV方法建立及GPV在实验感染雏鹅体侵染规律的研究

  20. Preliminary study on transcapsidation between GPV and GAV strains of Barley yellow dwarf virus

    大麦黄矮病毒GPV与GAV株系间异源装配现象的初步研究

  21. In this study , we designed primers that can directly differentiate GPV from MDPV using a single PCR reaction .

    本实验中设计出一组引子,能在于一次PCR反应中,直接区分是GPV或是MDPV感染。

  22. T1 plants of the transgenic lines ( 2 and 3 ) were indicated resistance to GPV to some extent .

    获得的2个转基因系的T1代苗在温室中的初步抗病检测显示,转基因后代对GPV株系具有一定抗性。

  23. Preparation and application of immunosera against GPV

    鹅细小病毒免疫血清的制备及其应用

  24. Determination on biology of strains of GPV and GAV transmitted by greenbug and English grain aphid

    麦二叉蚜、麦长管蚜传播小麦黄矮病毒病株系GPV、GAV的生物学特性测定

  25. The Fine Structure and Morphogenesis of Envelope and Nucleocapsid of GPV and IBRV : Freeze-Etching Study

    GPV和IBRV的超微结构与形态发生的冰冻蚀刻研究

  26. The nucleotide identity of the PCR product between HG5 / 82 and GPV strain B was 93.6 % .

    PCR产物序列与GPV参考毒株B的相应序列同源性达93.6%。

  27. Differentiation of Goose Paramyxovirus ( GPV ) and Newcastle Disease Virus ( NDV ) by Multiplex RT-PCR

    复合RT-PCR快速鉴别鹅副粘病毒与鸡新城疫病毒

  28. Further more recombinant GPV construction system and optimized the purification methods were established , which supply a technique platform for investigation of live vector vaccine and relative basal research .

    研究建立了表达外源基因重组GPV构建系统及其克隆纯化方法,为进一步开展GPV活载体疫苗研制及相关基础研究提供了技术平台。

  29. One wild strain of gosling plague virus ( GPV ) was isolated from the liver and spleen of affected young goose in GuangDong province .

    从广东某地死亡的、具有小鹅瘟典型病变的雏鹅肝、脾中分离到一株病毒。

  30. The result of sensitivity assay of hybridization showed that as little as 0.032 ng of GPV DNA could be detected by the DIG-labeled probe .

    敏感性检测结果表明该探针对GPV的最低检出量为0.032ng。