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our lab
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  本实验室
     Members of this family include avrxa5,avrXa7,avrXa10 ,and the avrXa3 which was cloned recently in our lab from the strain JXOⅢ of the bacterium from different races of Xoo .
     已报道的avrxa5、avrXa7、avrXa10以及本实验室从水稻白叶枯病菌菌株JXOⅢ克隆的avrXa3均属于avrBs3/ pth家族。
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     Our Lab also constructed an oncolytic adenovirus--ZD55-gene by deleting adenoviral E1B 55kDa gene.
     本实验室将腺病毒E1B 55kDa蛋白基因剔除后构建了另外一类肿瘤特异性增殖腺病毒ZD55-Gene。
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     (1) Our lab has previously cloned the liver-specific sequence-LFIRE-1 by DD-PCR.
     (1)本实验室已通过DD-PCR的方法克隆了一个人肝脏特异表达cDNA序列——LFIRE-1。
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     The Fc genes of Newcastle disease virus (NDV) strain LaSota E 4 and F 46 E 9 were recovered from the recombinants of pUCLaFc and pUCF 46 Fc constructed by our lab before.
     将新城疫病毒(NDV)F46E9株和LaSotaE4株的融合蛋白裂解位点(Fc)基因从本实验室构建的重组质粒pUCF46Fc和pUCLaFc中用EcoRI和SalⅠ切出。
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     The previous studies in our lab showed that LKS1 interact with AKT1 (Arabidopsis K~+ Transporter, a Shaker family potassium channel) in yeast two-hybrid experiments, and akt1 has the same phenotype as lks1 when treated under low potassium conditions.
     本实验室已有的研究显示:LKS1与钾通道AKT1(Arabidopsis K~+ Transporter)在酵母双杂交体系中互作:lks1与akt1在低钾处理条件下具有相似的表型。
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  “our lab”译为未确定词的双语例句
     Results The risk rates of down's syndrome and trisomy 18 syndrome were 2. 35% and 0. 35% by median of Access, but the risk of down's syndrome and trisomy 18 syndrome were 5. 46% and 0. 58% on our Lab. The screening positive rate of neural tube defects on two group both were 1.09%.
     结果:在1738 例孕妇中,按Access仪提供的中位数和本组孕妇的中位数计算,唐氏综合症(Down Syndrome,DS)筛查阳性率分别为2.35%,5.46%,18三体筛查阳性率分别为0.35%,0.58%,神经管缺陷(neural tube defects NTD)筛查阳性率均为1.09%。
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     Our lab previously reported CDK11P58, a G2/M CDK, acts as a partner of cyclin D3 in G2/M phase.
     我们实验室报导了一个G2/M期的CDK-CDK11P58,也能特异地与cyclin D3在G2/M期相互作用。
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     The sample is provided by our lab and accomplished by the Walter and Eliza Hall Institute for Medical Research of Australia.
     该项测定是由本实验室提供测定样品,并由The Walter and Eliza Hall Institute for Medical Research of Australia协助完成。
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     ECRG2 (Genebank AF 268198) and ECRG4 (Genebank AF 325503) are novel esophageal cancer suppressor genes cloned and identified in our lab.
     ECRG2(Genebank AF 268198)和ECRG4(Genebank AF 325503)是本室发现的新的食管癌相关抑癌基因。
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     Two prototypes of 1kV/420A/300ns/600W and 6kV/32A/500ns/500W palsed power supplies are developed in our lab. The experimental results show the correctness of the design.
     设计了两套运行参数分别为 1kV/4 2 0A/3 0 0ns/60 0W和6kV/3 2A/50 0ns/50 0W的IGBT脉冲电源装置 ,给出了实验结果
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     lab.
     lab.
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     Lab.
     Lab为开发环境建立。
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     strain B-2023 stored at our lab.
     strain B-2023,对其液体发酵产生纤溶酶(暂命名为BH-1)的条件进行了优化,用自制的猪血浆平板测酶的活性,得出以下结果:
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     The progresses of recent years in our lab are introduced.
     本文介绍了环境断裂近年来的研究进展。
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     To Our Readers
     致《国外城市规划》的读者
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  our lab
The predictions of the model are shown to compare well with the experimental results obtained in our lab and with the literature data.
      
Published work from our lab has shown that our 3-D models respond to infection with bacterial and viral pathogens in ways that reflect the infection process in vivo.
      
Within the context of the UK Government Project "Grid-oriented Storage (GOS)" and the EC Project "EuroAsiaGrid," GOS has been developed in our lab, which melds parallel streaming technique to meet the needs of WAN/Grid-based virtual organizations.
      
Two types of highly active and selective vinyl acetate monomer (VAM) catalysts have been developed in our lab via traditional lab preparation and high-pressure reactor performance test methods.
      
Further refinements of assessment techniques used in our lab are briefly described.
      
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This article describes the material-and-device processing of GaP green LED's. Measurement and analysis on both material and devices obtained in our lab. have shown that LPE with overcompensation technique is successful in growing green-light-emitting PN junctions with high reproducibility, and following performances have already been obtained: forward Voltage drop<2.7v. at 30 mA, total light flux is 10~20 mlu. at 30 mA, and peak emitting Wavelength~5600(?)。

文章叙述了GaP绿色发光二极管的材料和器件的制备。对试验所得到的这些材料和器件进行测定与分析表明:用过补偿液相外延方法已能重复地生长出绿色发射PN结。目前已达到的绿色发光二极管性能为:30毫安电流下,正向压降低于2.7伏,总光通量普遍大于10毫流明,有些高达20毫流明以上;发光光谱峰值波长为5600埃左右。

A technique has recently beendeveloped in our lab for isolation ofembryo sacs by enzymatic macerationof fixed ovules (Zhou and Yang1982).The present paper is an ex-tension of this work.Intact embryosacs were successfully isolated fromfixed as well as fresh ovules of Antirr-hinum majus.The method used onfixed ovules was similar to that des-cribed previously.A series of figuresincluding mature embryo sacs priorto fertilization,entry of pollen tube,and embryo sacs after fertilization with2,4,8 and multicellular...

A technique has recently beendeveloped in our lab for isolation ofembryo sacs by enzymatic macerationof fixed ovules (Zhou and Yang1982).The present paper is an ex-tension of this work.Intact embryosacs were successfully isolated fromfixed as well as fresh ovules of Antirr-hinum majus.The method used onfixed ovules was similar to that des-cribed previously.A series of figuresincluding mature embryo sacs priorto fertilization,entry of pollen tube,and embryo sacs after fertilization with2,4,8 and multicellular endospermwere identified in macerated materi-als.Isolation of viable embryo sacswas carried out with fresh ovules,whichwere macerated in a mixture solutionof 2% pectinase and 1—1.5% cel-lulase with or without mannitol and/or potassium dextran sulphate by amicroshaker at 28—30℃ for 2—3hours.Embryo sacs both before andafter fertilization were isolated fromfresh materials,though their cellularstructure was not as clear as fixedones.Histochemical reactions revealed that these embryo sacs were richof ergastic substances,such as lipiddrops,polysaccharide and starchgrains.The significance of isolation ofviable embryo sacs in view of furthercytochemical and cytophysiologicalstudies and in vitro culture of embryosacs is discussed hereof.

用果胶酶与纤维素酶的混合液离解金鱼草的胚珠,从中分离出完整的胚囊。由固定材料分离的胚囊,经透明染色后可借助干涉差显微装置观察由受精前直至受精后具上百个胚乳细胞时期的胚囊的内部结构。由新鲜胚珠分离胚囊也已初步突破,并对其作了简易的显微化学观察。讨论了活胚囊分离的意义与胚囊离体培养的前景。

Inspection of hypodermic syringe needle tips has been performed in our lab using an optical spectrum analysis system. The statistic processing method realized by a digitial computer is presented. The experimental results indicate that the minimal measurable defect size of damaged needle tips approaches the curvature radius of normal needle tips. When the defect size a is over 0.02mm, inspection ratio η is greater than 94.5%.

报道了利用光学频谱分析系统对注射针尖进行质量检验的实验,给出了测!数据统计处理方法。实验结果表明,对针尖尖锐度的检测已达到针尖曲率半径之极限范围,对于针尖平度数a>0.02毫米的次品针尖检出率η>94.5%。

 
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