1、

Typing of NA Gene in the Hui Nationality in North west China by PCR SSP

PCR-SSP方法对西北地区回族NA抗原基因分型

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2、

Screening of Antagonistic Actinomycetes against Animal Pathogen from Saline Soil of Northwest Typing of NA Gene in the Hui Nationality in North west China by PCR SSP

西北地区盐渍土中抗动物病原菌的拮抗放线菌筛选PCR-SSP方法对西北地区回族NA抗原基因分型

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3、

Methods: PCR technique was used to determine the ACE gene genotypes in 102 cases of Chinese type ⅱ diabetics.

方法:用PCR技术检测102例中国汉族Ⅱ型糖尿病患者ACE基因I/D多态基因型。

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4、

Chitinase gene had been amplified by PCR in albinos lethal mutant line, that certificated transformation was successful;

PCR扩增结果表明在白化致死突变株系中存在几丁质酶基因,证明转化成功;

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5、

One step RT-PCR is practisible for ARV RNA detection.

表明该一步法RT_PCR对于ARV的检测是可行的.

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6、

Detection and Identification of Food Borne Pathogens Using Real Time PCR and Gene Chip Assay

运用实时荧光PCR和DNA芯片技术检测和鉴定食源性致病菌方法的研究

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7、

During the course of prenatal diagnosis we discovered a previously undescribed β-30 TATA box mutation ( T → C) by using PCR and direct DNA sequencing.

在产前诊断过程中,我们应用PCR后直接DNA测序技术发现一种以前未描述过的突变:β-30(T→C)。

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8、

Rz 107 was electroporated into BRL-3 A cells and the Rz 107 expression was analyzed by RT-PCR.

将携带有Rz107基因的真核表达质粒pcDNA31Rz107电穿孔至BRL3A细胞中,通过RTPCR方法分析Rz107的细胞内剪切活性.

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9、

Genotyping of the PCR-amplified isolate from the confirmed case shows high homogeneity with other H5N1 isolates from poultry in Java, and no evidence of reassortment.

对确认病例的PCR扩增分离菌进行基因型确定,显示与爪哇禽类的其它H5N1分离菌具有很高的一致性,没有重新分类的依据。

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10、

Method Chelex 100 extraction method was used to extract DNA of 170 cigarette butts, STR loci were typed after PCR amplification by Profiler Plus kit.

方法用Chelex-100法提取170枚烟蒂样本的DNA,进行PCR扩增及STR检验。

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11、

Semiquantitative RT-PCR determination of specific glycosyltransferases may be helpful for diagnosis and prognosis of BDC.

采用半定量RTPCR检测糖基转移酶的表达,将有助于对胆管癌的诊断和预后判断.

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12、

Objective To establish multiple PCR assay for simultaneous detection of agents causing genital ulcer disease ( GUD).

目的建立多重PCR用于快速检测引起性传播生殖器溃疡性疾病(GUD)常见病原体。

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13、

A watermelon mosaic virus 2 ( WMV-2) isolate from diseased watermelon in Shanxi Province was used for cDNA synthesis of WMV-2 CP gene by RT-PCR.

本研究以从山西西瓜上分离纯化得到的西瓜花叶病毒2号(WMV-2)分离物为材料,用RT-PCR方法得到其外壳蛋白(CP)。

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14、

Optimized RAPD-PCR reaction system by orthogonal design, and DNA polymorphism for RAPD analysis of Metarhizium anisopliae isolate from different areas.

通过正交设计试验优化了绿僵菌RAPD-PCR反应体系,并对不同地理来源金龟子绿僵菌进行DNA多态性RAPD分析。

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15、

Conclusion: PCR technique is the most sensitivity and differential method.

结论:4种方法中以PCR检测法的灵敏性和特异性最高,抗体检测法次之。

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16、

Development of a competitive PCR assay for quantifying sheep-associated malignant catarrhal fever viral DNA

定量测定羊关联性恶性卡他热病毒DNA的竞争性PCR方法的建立

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17、

By polymerase chain reaction ( PCR), the seasonal variation of the phytoplasmal amounts in mulberry tree was determined.

通过聚合酶链式反应(PCR)检测了植原体在桑树体内的分布及其相对含量的周年变化。

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18、

In addition, the two RT-PCR reaction systems of Apple scar skin viroid and Apple mosaic virus, which cause serious harms on apple production, were optimized and established the more simple and efficient detection assay. 2.

另外,对生产上危害较重的苹果锈果类病毒和苹果花叶病毒的RT-PCR反应体系进行了优化,建立了操作步骤更简单、效率更高的RT-PCR检测体系。

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19、

Detection of human papillomavirus type 16 DNA by quantitative PCR in cervical dysplasia tissues

宫颈非典型增生组织中HPV16-DNA的定量PCR检测

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20、

Methods Telomerase activity in 28 specimens of cervical carcinoma, 6 specimens of cervical dysplasia and 10 specimens of normal cervical tissues were detected by PCR based sliver staining Telomeric repeat Amplification Protocal ( TRAP).

方法:采用PCR TRAP方法对28例宫颈癌组织,10例正常宫颈组织,6例宫颈不典型增生组织的端粒酶活性进行检测。

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