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Original playlists let you group, arrange and manage your records, the extended graphical equalizer let you change speed of playback, amplify weak signals and add such sound effects as flanger, echo and reverberation.

原始列表让你可以分组，整理和管理你的唱片，扩展的图形化均衡器让你可以改变回放的速度，放大弱小的信号以及添加诸如重复，回响这样的声音特效。

A multiplex PCR assay for detection of Escherichia coli O157:H7 was developed by using 3 sets of primers that specifically amplify segments of the rfbE、fliC and eaeA genes. The target genes fragment of the PCR assay were 291 bp, 625 bp and 368 bp, respectively. Analysis of 30 strains demonstrated that this PCR system was specific.

以编码大肠杆菌O157抗原的rfbE基因、编码H7抗原的fliC基因以及编码毒力因子的eaeA基因为靶基因，选择3对引物，建立并优化了检测大肠杆菌O157：H7的多重PCR体系，扩增产物分别为291 bp、625 bp、368 bp，采用30株细菌验证了该多重PCR具有特异性。

The study cloned the flic gene of App and performed sequencing and analysis of biological information. Polymerase chain reaction PCR was used to amplify the flic gene from.

构建猪传染性胸膜肺炎放线杆菌(Actionobacillus pleuropneumoniae， App)鞭毛蛋白编码基因的重组表达质粒，对其编码蛋白进行生物信息学分析，并将其在原核细胞中进行表达。

The technique is requires a thermal cycling process to amplify target DNA strand in vitro, intercalation of labeling into the amplified DNA strand, and detection of the variation of fluorescence intensity of labeling dye during the amplification of DNA strand a Fluorimeter.

此技术，主要需结合温控机构与萤光分析仪，在温控过程进行DNA体外增生，同时监控增生过程中DNA嵌合萤光萤光强度的变化，进行定量分析，实现此技术之仪器被称为即时侦测同步定量聚合酶连锁反应器(Real-time PCR machine)。

Firstly, by the addition of formamide to 8% into the reaction buffer, conventional PCR technique is used to amplify the GC-rich TGF β1 mature peptide gene encoding the TGF β1 monomer.

首先，采用常规的PCR技术，通过在反应混合物中加入8％的甲酰胺，成功地扩增了高GC含量的、编码人TGFβ1单体分子的成熟肽基因。

In this paper, degenerate PCR was used to amplify the DM domains of Dmrt genes in Gallus gallua.Domesticus.

通过简并PCR克隆技术，扩增和克隆了家鸡基因组中的DM结构域，经序列分析，获得了两个具有不同DM序列的克隆，分别命名为GgDmrt2和GgDmrt5。

The ORF2 gene is the most important protein-code gene for porcine circovirus, and is the main gene differing porcine circovirus typel from porcine circovirus type2 (PCV2). To construct a specific PCR detecting method, we designed a pair of primers to amplify a partial fragment of ORF2 gene from PCV2, referring to fifteen strains complete genome published in Genbank. The PCR product was about 0.67kb in size detected by gelose gel electrophoresis.

猪圆环病毒的开放阅读框2(ORF2)是其主要结构蛋白的编码基因，也是区分猪圆环病毒1型(PCV1)和猪圆环病毒2型(PCV2)的重要基因，本研究参照GenBank已发表的15株PCV2基因序列，设计合成一对引物，对PCV2的ORF2基因进行PCR扩增，产物经琼脂糖凝胶电泳，呈现一条大小约0.67kb的特异条带，经条件筛选，建立了猪病料中PCV2感染的PCR检测方法。

Traditional image enhancement technique will amplify interfering signal and scintillation at the same time, while grey scale accelerating circuit and contrast enhancement technology have successfully solve this problem.

传统的影像增强技术会使干扰信号和闪烁也同时被放大，灰阶加速电路和对比度增强技术成功地解决了这个问题。

We couldn't see the line-relationship of the mute sites and the feather color types; maybe MC1R was just one major but not only silky feather color functional gene, the feather color maybe controlled by several genes. 8. There were length differences when using the same primer to amplify the mtDNA HVS-1 of black normal feather Wugu chickens and Guinea fowl.

在这些突变的氨基酸位点中，突变与羽毛颜色间除了丝羽乌鸡外均有一一对应关系，这可能提示乌鸡的丝羽口及颜色受多个基因的调控，MC IR基因可能是其中的一个主效但不是唯一的质量性状基因。

We couldnt see the line-relationship of the mute sites and the feather color types; maybe MC1R was just one major but not only silky feather color functional gene, the feather color maybe controlled by several genes.8. There were length differences when using the same primer to amplify the mtDNA HVS-1 of black normal feather Wugu chickens and Guinea fowl.

在这些突变的氨基酸位点中，突变与羽毛颜色间除了丝羽乌鸡外均有一一对应关系，这可能提示乌鸡的丝羽口及颜色受多个基因的调控，MC IR基因可能是其中的一个主效但不是唯一的质量性状基因。

He and Nina moved to California and lived at 2005 Ivar Street, Apt.

他和Nina搬到加州，并在2005年伊瓦尔街，公寓生活。

Droperidol （ potently inhibits transfected HERGchannels and this is the probable mechanism for QT prolongation.

氟哌利多有效地抑制了转染的 HERG 钾通道，可能是 QT 间期延长的机制。