1、

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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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、

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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4、

Detection of feline panleukopenia virus infecting tiger by PCR

用PCR法检测东北虎感染猫细小病毒的研究

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5、

Development of one step Real-time RT-PCR method for detection of Hendra virus

Hendra病毒一步法Real-Time RT-PCR检测方法的建立

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6、

Detection of Hendra virus by real-time PCR assay

Hendra病毒的实时PCR检测方法的建立

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7、

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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8、

The results showed that the typical expressions of GVHD were observed 4 or 5 days after the injection of donor spleen cells, and specific male Y chromosome fragment was amplified by genomic PCR in female BALC/ c receipts.

结果显示:3注射脾细胞4~5天后,小鼠开始出现GVHD典型体征,第10天受体小鼠体内扩增出雄性供体小鼠Y染色体特异片段。

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9、

The library was screened by using 20 microsatellite markers and 5 known functional genes with PCR. Positive BACs for all these markers and genes were identified successfully and the positive number ranges from 3 to 19 with average of 11.3.

用20个微卫星标记和5个功能基因对整个文库进行PCR筛选,所有这些标记和基因都得到了阳性克隆,克隆数从3到19不等,得到的平均阳性克隆数为11.3。

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10、

C 3 d-P 28 coding gene was amplified by PCR.

将PCR获得 的补体C3d-P28DNA序列 以头尾串连的方式构建四聚体.

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11、

PCR founded in 1985, as a amplification technology in vitro, it acts in life science study importantly in recent ten years.

PCR是1985年兴起的一项基因体浙江大学硕土学位论文外扩槽的分于生物学新技术,多年来在生命科学研究领域发挥了前所未有的作用。

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12、

Application of real-time fluorescence quantitative PCR accompanied with comparison of Delta CT for diagnosis of Down's syndrome from a single cell

单细胞实时荧光定量PCR结合比较阈值法在诊断唐氏综合征中的应用

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13、

The PCR and hybridization results were compared.

将唐氏综合征患者的荧光定量PCR检测结果和荧光原位杂交检测结果与细胞遗传学分析结果进行比较。

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14、

The Investigation of the Application of Quantitative Fluorescent PCR for Fast Prenatal Diagnosis of Down's Syndrome

定量荧光PCR在唐氏综合征快速产前诊断中的应用研究

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15、

Conclusion Real-time FQ-PCR is a reliable method that may provide a new way for non-invasive prenatal diagnosis and preimplantation genetic diagnosis for Down's syndrome.

结论实时荧光定量PCR是一种可信的诊断方法,为唐氏综合征的无创性产前诊断及植入前遗传学诊断等提供了新的思路。

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16、

The relationship between genital tract cytomegalovirus infection and tubal pregnancy DETECTION OF HUMAN CYTOMEGALOVIRUS BY PCR

输卵管妊娠患者生殖道巨细胞病毒检测与基因分析人巨细胞病毒的PCR检测

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17、

Clinical Significance of PCR Techique in Detecting the Infection of Male Urinary Tract

PCR法检测男性泌尿道感染的临床意义

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18、

Method The genotypes and alleles of D4 receptor gene in 104 refractory schizophrenic patients and 76 healthy controls were examined with PCR amplification technique.

方法用PCR技术测定104例难治性精神分裂症病人和76例正常人的D4受体基因。

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19、

Conclusion : FQ-PCR is absolutely necessary methods for diagnosis CMV infection in pregnant women.

结论FQ -PCR 对CMV感染的诊断有重要的作用.

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20、

RT-PCR for Diagnosis of Rubella and Analysis on E1 Region DNA Sequencing

RT-PCR诊断风疹及E1膜蛋白基因序列分析

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