聚合酶

The strain BEB2 of endophytic Bacillus isolated from banana was identified as Bacillus subtilis according to its homology analysis of 16S rDNA sequence. The temperature, pH and medium had a significant impact to the inhibition of BEB2 to the banana wilt disease.

利用聚合酶链式反应方法对细菌BEB2做进一步的分子鉴定，并研究不同温度、pH值和培养基下BEB2发酵液对香蕉枯萎病菌生长的抑制能力，以及应用BEB2对香蕉枯萎病进行防治测试。

Methods: 70 patients with COPD and 70 healthy volunteers were enrolled in this study. Limosis peripheral blood was taken and whole blood corpuscle genomic DNA was extracted. The genetic polymorphism of SOD1-3 genes was determined by polymerase chain reaction and restriction fragment length polymorphism.

收集70例COPD患者和70例健康人空腹外周血，提取全血细胞DNA，采用聚合酶链式反应－限制性片段长度多态性法检测两组SOD1-3基因的多态性。

Borna disease virus ; Reverse transcription-polymerase chain reaction ; Receptor ; Serotonin ; Dopamine ; Transcription ; genetic

Borna病病毒；逆转录聚合酶链反应；受体；血清素；多巴胺；转录；遗传

The total RNA of viruses isolated was extracted from the Hantavirus-infected Vero-E6 cells and the S-segment cDNA of Hantavirus was obtained by RT-PCR. This gene fragment was then cloned into plasmid vector pUCm-T and sequenced afterwards by using the DNA STAR software for comparison.

提取病毒总RNA，应用逆转录聚合酶链反应扩增病毒S基因全片段，克隆入质粒载体，进行核苷酸序列测定及分析，应用DNA STAR软件分析比较，确定病毒型别。

Methods: Four hantavirus strains, which were positive by antigen immunofluorescence assay, were analyzed by reverse transcription polymerase chain reaction, nucleotide sequence and cell culture.

采用逆转录－聚合酶链反应、核苷酸序列测定和细胞培养方法对免疫荧光抗原阳性的4份鼠肺标本进行汉坦病毒分析。

A virus strain was isolated from samples of oviduct mucosa of breeder duck , which showed irregularity and reduction in egg-laying.

从表现产蛋异常的蛋鸭中分离到1 株病毒，经血凝抑制试验和聚合酶链反应方法鉴定为H9N2亚型禽流感病毒。

Nine different aphid-resistant alfalfas and four cross bred F1 were used in this experiment to investigate better dosage in SSR technique system and to seek the best combination among factors.At last,the best SSR technique system was established. The Taq DNA polymerase was 0.2μL(5U/μL),the 10×Buffer(Mg2+Plus)was 2.5μL , the dNTP Mixture was 2μL ( 2.5mmol/L), the primer was 1.5μL (10μmol/L),the template DNA was 1μL,the ddH2O was 16.3μL ,and the whole system was 25μL.

以九个不同抗蚜级别的苜蓿品种及四个杂交F1代为试材，摸索SSR反应体系中各个影响因素的浓度和用量，确定适合苜蓿抗蚜虫基因定位的SSR反应体系：其中Taq DNA聚合酶0.2μL(5U/μL)，10×Buffer(Mg2+Plus) 2.5μL，dNTP Mixture 2μL (各2.5mM)，引物各1.5μL (10μM)，模板DNA1μL，ddH2O 16.3μL补足25μL。

Methods Polymerase chain reaction with two groups of common primers for TCR-γ gene was used to analyze the malignant cells of 28 autopsied cases of malignant histiocytosis.

方法用两组针对T细胞受体γ链的通用引物和聚合酶链反应，对28例&恶组&的尸检病例进行了TCR-γ基因重排的检测。

But the overseas MMP-1-associated cases of oral cancer lacked those of Taiwan, where there are many betel nut chewers. Therefore, this research aimed at Taiwan, to analyze the MMP-1 expression of oral cancer in the just- mentioned patients.

共选取了奇美医学中心口腔颚面外科 30 位只具有长期嚼食槟榔并接受口腔癌手术切除的患者，分别进行肿瘤样本组织与肿瘤周围组织中 MMP-1 的半定量反转录作用-聚合酶连锁反应，发现在肿瘤样本组织中 MMP-1 mRNA 有普遍提高的表现。

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。

It has been put forward that there exists single Ball point and double Ball points on the symmetrical connecting-rod curves of equilateral mechanisms.

从鲍尔点的形成原理出发，分析对称连杆曲线上鲍尔点的产生条件，提出等边机构的对称连杆曲线上有单鲍尔点和双鲍尔点。

The factory affiliated to the Group primarily manufactures multiple-purpose pincers, baking kits, knives, scissors, kitchenware, gardening tools and beauty care kits as well as other hardware tools, the annual production value of which reaches US$ 30 million dollars.

集团所属工厂主要生产多用钳、烤具、刀具、剪刀、厨具、花园工具、美容套等五金产品，年生产总值3000万美元，产品价廉物美、选料上乘、质量保证，深受国内外客户的青睐