DPV

Confirmed that the method can be used in clinical detection of DPV .

证实该方法可应用于临床DPV的检测。

The results will help us to study the diagnosis and pathogenic mechanism of DPV .

该结果有利于对鸭瘟病毒的诊断及致病机理的研究。

This is the first report of the DPV genes above .

这是国内外对鸭瘟病毒以上基因序列的首次报道。

Compared with other alphaherpesviruses , the total level of DPV study is much lower .

相对其它α-疱疹病毒而言，DPV研究的总体水平较低。

Study on Molecular Characterization of Intestinal Microbial Community of Ducks Infected with DPV Virulent Strain

DPV强毒感染鸭肠道菌群的分子解析

It was concluded that there were no significant differences between the results obtained by the DPV and those obtained by the HPLC method .

HPLC分析进行t检验，测定结果无显著性差异。

DPV U_L26 Gene Prokaryotic Expression and the Study of Its Cellular Localization in Virus-infected Host Cells

鸭瘟病毒UL26基因原核表达及宿主细胞中的定位研究

A rather low detection limit of AA is obtained with DPV measurement using MWNT / GCE as working electrode .

应用MWNT/GCE对AA以微分脉冲伏安法测定得到了很低的检测限。

Effect of " Shuanghuang " granula against DPV in duck embryo

双黄在鸭胚中抗鸭瘟病毒的效力试验

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。

The results showed that DPV exhibited higher sensitive and lower detection limit for the determination of target , compared with the results using UV-vis spectra analysis techniques .

结果表明电化学方法较紫外可见分光光度法更适合用于物质的微量检测。相比之下其灵敏度更高、检测限更低。

The duck parvovirus disease is an acute and contagious disease caused by the Duck Parvovirus ( DPV ) .

鸭细小病毒病是由鸭细小病毒（duckparvovirusDPV）引起，以雏鸭为易感的急性传染性疾病。

The DPV peak currents decreased with the increased AFP concentration due to increasing spatial blocking and impedance from the formed immunoconjugates .

随着AFP抗原浓度的增加，由于形成的免疫复合物的影响而导致的空间位阻和阻抗的增加，从而引起了DPV峰电流的降低。

There , it can be infered from the distribution pattern that DPV gI was expressed in cytoplasm .

因此，从gI蛋白的分布特征可以推测该蛋白主要在细胞质中合成。

MPCs / electrode interfacial structure and electrochemical properties of nanometer-scale electrode interface are studied by CV , DPV and EIS .

采用循环伏安法、示差脉冲伏安法、电化学阻抗谱技术研究自组装MPCs电极界面的结构和纳米尺度电极界面的电化学性质。

The result of the study will provide significant testing data for illuminating nosogenesis of DPV and detecting DPV by PCR in infected duck body .

结果为阐明DPV的致病机理和应用PCR方法检测感染鸭体组织中的DPV提供了重要的实验数据。

The ambroxol hydrochloride was determined with a carbon fiber electrode modified with bismuth film by differential pulse voltammetry ( DPV ) at1 .

介绍了一种制备碳纤电极的新方法，并研究了盐酸氨溴索在铋膜修饰的碳纤电极上的电化学响应。

The optimal condition of the DNA fixed and hybrid was confirmed by electrochemical characterization ( CV , DPV , EIS ) compared with different material modified electrode .

采用CV、DPV、EIS电化学方法对不同材料修饰的电极进行电化学测试对比，确定了DNA固定与杂交的最佳条件。

The results of continuous passage showed that the DPV - △ gE-EGFP was able to be stably inherited and express EGFP protein .

连续传代结果说明DPV-△gE-EGFP能够稳定遗传并表达EGFP蛋白。

A method to determine pyrocatechol and p-dihydroxybenzeqe in the presence of each other with carbon paste electrode by DPV was reported .

本文介绍用示差脉冲伏安法（DPV）采用自制的碳糊电极同时测定邻苯二酚与对苯二酚的方法。

DPV is an objectively and quantificationally indicator , hence an useful climate diagnosis tool to diagnose seasonal transition and the Indian summer monsoon onset .

该变差度可客观定量的诊断季节变化和夏季风建立的时间，是一个好用的气候诊断工具。

In the first direct catalytic oxidation method , we studied the catalytic oxidation behavior of EDTA on graphene-modified electrode with differential pulse voltammetry ( DPV ) .

直接催化氧化法：用差示脉冲伏安法（DPV）研究EDTA在氧化石墨烯修饰电极上的催化氧化行为。

The enriching mechanism was investigated by using open circuit potential-time technology ( Op ~ t ), cyclic voltammetry and differential pulse voltammetry ( DPV ) .

用开路电位时间谱技术（Op～t）、循环伏安法（CV）和微分脉冲伏安法（DPV）表征了该溶液还原法对铜进行选择性富集的机理和效果。

The increasing transcription of DPV gI in the late infection stage suggests that DPV gI protein may closely related to the assembly and maturation of DPV .

DPVgI基因在感染晚期大量转录的现象提示基因编码产物可能参与成熟病毒粒子的囊膜化装配。

Under the optimum conditions , quantitative determination for ractopamine , isoxsuprine , ritodrine and fenoterol was carried out by DPV .

在最佳实验条件下，采用DPV对莱克多巴胺以及异克舒令、利托君和非诺特罗进行了定量测定。

The result indicate that the DPV DNA can be firstly detected 2 hours after inoculability from brain , liver , spleen , bursa of fabricius , thymus .

结果表明，接种2小时后即能够从脑、肝、脾、法氏囊、胸腺中检出DPVDNA。

The results showed that the biotinylated DNA probe could detect purified homologous DNA target at 10 pg level and could detect DPV DNA in 10 ~ 5-fold dilution of the liver tissue .

试验结果表明，生物素标记核酸探针可检出10pg提纯的鸭瘟病毒DNA，并检出稀释10~5倍和肝组织鸭瘟病毒DNA；

Detection the Varietal-regularity of Enteron and Respiratory Tract 's Bifidobacterium , Bacillus , Enterococcus with FQ-PCR for Duck after Artificially Infected by DPV

FQ-PCR检测DPV强毒人工感染鸭消化道及呼吸道双歧（芽孢）杆菌和肠球菌数量变化规律研究

The primers amplified a 101 bp fragment between the sites 891-991.With DNA obtained from standard virulent strain of DPV , a real-time quantitative PCR for DPV was established successfully .

以DPV标准强株DNA为模板，建立了实时荧光定量PCR检测鸭瘟病毒的方法。

The electrochemical behavior of kojic acid with a glassy carbon ( GC ) electrode was investigated . The contents of kojic acid were measured by differential pulse voltammetry ( DPV ) .

考查了曲酸在玻碳电极上的电化学行为，示差脉冲伏安法（DPV）可应用于测定曲酸，然而测定样品时裸电极的稳定性差；