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sequenced相关的网络例句

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The appraisal and the finding of current mill condition , the forecasting of conditiontrend ,fault diagnosis 、maintenance strategy arithmetic and decision-making deducingprocess.To enhance software function of equipment management information system, mill condition-based maintenance software aided system is developed,it can save mill condition data into equipment information management platform,through mill software module to analysis sequenced detection data and automaticly give the appraisal of current mill condition , the forecasting of condition trend ,fault diagnosis,maintenance strategy and decision-making suggestion for mill technician as a reference to decide whether tostart mill condition-based maintenance.

在燃煤电厂既有的设备点检和大小修管理信息系统软件平台的基础上,进一步开发磨煤机的状态检修软件支持系统模块,能存储磨煤机的状态点检数据入设备信息管理平台,通过磨煤机状态检修软件支持系统模块对一段时间内的磨煤机点检数据进行处理从而给出磨煤机当前状态的分析与评价,磨煤机状态趋势的预测,磨煤机的故障分析、故障原因查找和解决措施,将最终的维修决策建议提供给磨煤机的专业技术维修人员和管理决策者参考,结合软件分析和人工经验的干预以决定是否开始磨煤机的状态检修。

One fragment of 248 bp cDNA of the GABAa recep tor gene from the fourth instar larvae of diamondback moth was amplified, cloned, sequenced and analyzed by using reverse transcription polymerase chain reaction method.

利用反转录多聚酶链式反应对小菜蛾的γ-氨基丁酸a 受体基因cDNA片段进行了克隆和序列分析。

For five Enterobacteriaceaes tested for ESBLs by double-disk method, two primers were designed and synthetized: TEM-1and SHV-1, ESBLs gene type was amplified, sequenced and analyzed by PCR; the minimal inhibitory concentrations of Cetiofur combined BLI-Tazobactam to the five Enterobacteriaceae according to different proportions were carried out with two fold dilution method.

对产生ESBLs的5株致病性大肠埃希氏菌,设计并合成TEM-1和是SHV-12对引物,用PCR方法进行了ESBLs的DNA扩增、测序和基因型分析;用试管二倍稀释法测定头孢噻呋与BLI-他唑巴坦钠以不同配比对产生ESBLs大肠埃希氏菌的最小抑菌浓度。

In partⅢof the study,mitochondria DNA nad4 of the dog cestodes have been studied.The mtDNA nad4 were cloned and sequenced.

根据绦虫的部分序列设计的一对引物,经过PCR扩增犬绦虫线粒体nad4基因序列,克隆及测序。

Methods Tyresine kinase genes of EGFR (exons 18, 19 and 21) were amplified by PCR technology, and sequenced and analyzed by Chromas software in 80 NSCLC patients.

方法应用聚合酶链反应,对80例手术切除NSCLC瘤组织EGFR基因的第18、19和21外显子片段进行扩增和测序,Chromas软件分析基因突变。

The internal transcribed spacer (ITS, contains ITS-1, 5.8S nuclear ribosomal DNA, ITS-2) and 28S nuclear ribosomal DNA-LSU were amplified by PCR, sequenced and analyzed by Chromas and DNASTAR softwares, and the RNA secondary structure of 28S rDNA-LSU was analyzed by DNAMAN software.

抽提成虫基因组DNA,扩增其ITS(包括ITS-1、5.8S rDNA和ITS-2)和28S rDNA-LSU序列,测序并分析以上序列,以及28S rDNA-LSU序列RNA二级结构。

The four proper complete DNA sequences were obtained by splicing the sequenced results with the software SeqMan of the DNA Star. The homology compare of the corresponding nuclear sequences and the cladogram analyze between the obtained virus strain and abroad virus collate strain were measured by Jotun Hein method in software DNA Star.

将MS-1、DL-1、DL-2和DL-3株病毒经组织病料提取总DNA,采用依据标准毒株ADV-G的DNA序列设计并合成的四对引物,经PCR扩增后分别构建重组质粒并测序,将测序结果用DNA Star软件中的SeqMan程序进行拼接,获得四株病毒的近全长DNA序列。

The positive colones were screened and then the inserted fragments were sequenced.

此外 ,NS3、NS5和 3′NTR的几个位点可能与病毒毒力稳定性相关。

Speculating on the figure of two dimensional electrophoresis of rice glutelins there are at least 13 glutelin genes, only six of which, GluA-1, GluA-2, GluA-3, GluB-1, GluB-2 and a cDNA clone,λ RG21 cDNA, have been sequenced.

从水稻谷蛋白的2-D电泳可推测,编码水稻谷蛋白的基因至少有13个,目前尚只有6个水稻谷蛋白基因被分离测序,它们分别是GluA-1,GluA-2,GluA-3,GluB-1,GluB-2和一cDNA克隆(λRG21 cDNA),而且,这些基因都是通过实验筛选大量的水稻基因组文库或cDNA文库获得的,其过程成本高,工作量大,实验周期长。

Methods Four probands from four unrelated families with typical manifestations of CADASIL were studied The 1~12 coding exons and their flanking intron sequences of NOTCH3 gene were amplified by PCR and sequenced Some family members in the pedigree 2 and 4 were also examined for the NOTCH3 gene mutations Results Four hete...

结果 4个家系中的先证者均发现有NOTCH3基因的杂合性错义突变,先证者 1为外显子 3的 2 6 8C→T突变,先证者 2为外显子 3的 32 2C→T突变,先证者 3为外显子 3的 32 8C→T突变,先证者 4为外显子 11的 1819C→T突变,分别造成Notch3蛋白质R90C、C10 8R、R110C和R6 0 7C 4个位点氨基酸的替换。

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