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polymorphism相关的网络例句

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与 polymorphism 相关的网络例句 [注:此内容来源于网络,仅供参考]

The present study provides experimental data to understand ADH enzymic property, and to explore the relationship between polymorphism of ADH activity and disease.

该研究为进一步了解ADH酶学性质,探讨酶活性多态性与疾病的关系打下基础。

The present study provides experimental data to understand ADH enzymic property, and to explore the relationship between polymorphism of ADH activity and disease.

为进一步了解ADH的酶学性质,探讨ADH与疾病的关系,本文构建了人ADH原核表达载体,进行了体外表达,并测定了部分酶学参数。

Some intergeneric hybrids (Sugarcane×Erianthus fulvus) were identified by chromosome counting and RAPD (Random Amplified Polymorphism DNA) technique.

采用体细胞染色体计数和RAPD(Random Amplified Polymorphism DNA)分子标记的方法鉴定甘蔗与蔗茅属间杂交种F1的真实性。

The reaction system of AFLP (Amplified Fragment Length Polymorphism) in genus Eriobotrya was studied and the AFLP analysis system was established by detected the results of several reactions such as DNA extraction, enzymes restriction, adapter-ligation, pre-amplification and selective amplification; the main factors which affected AFLP analysis were analyzed.

通过检测AFLP分析中DNA提取、酶切及连接、预扩增和选择性扩增的结果,对影响AFLP分析的主要因子进行分析,建立了AFLP分析体系。

Objective To investigate the association between MBD3 gene polymorphism and schizophrenia and provide theoretical basis for its etiological study.

目的:探讨MBD3基因多态性与精神分裂症的关系,为精神分裂症的病因学研究奠定基础。

Five of fifty random primers amplified DNA polymorphism hands in RAPD analysis of seed-derived seedlings and of in vitro regenerated plantlets taken at random. One primer eyen amplified the difference between the regenerated plants. This suggested that there was some variation in DNA in plants of M. sativa regenerated in vitro.

随机选取实生苗和下胚轴愈伤组织再生苗进行RAPD分析,结果表明,所用的50个随机引物中有5个扩增出差异性条带,甚至再生植株之间也有1条引物扩增的条带有差异,这说明经组织培养所得到的再生植株与实生苗相比,在DNA水平上发生了一定程度变异,并且这种变异也存在于再生植株之间。

By using random amplified polymorphic DNA technique, this paper studied the effects of Cd stress on DNA polymorphism in root tip of Vicia faba seedlings.

采用随机扩增多态性DNA技术检测镉胁迫对蚕豆幼苗根尖DNA多态性的影响。

The gene polymorphism of PPARγC161-T was an independent risk factor which was associated with the occurrence of CHD after farraginous factors were excluded.

逐步logistic回归方法分析得CT基因型为排除混杂后与冠心病发病显著相关的独立危险因素。

By using SRAP technology, a polymorphism primer of E2M5 was successfully selected. The primer E2M5 can be used to test hybrid purity of a small fruited diploid watermelon variety Hongxiaoyu.

采用SRAP技术,成功筛选出1对多态性好的引物对E2M5,对二倍体小果型西瓜品种红小玉杂交种纯度开展了分子鉴定研究。

Drug sensitive test and three-dimensional test220 strains of Pa were isolated from hospitalized patients between 2003 and 2007. K-B method was used to tested the susceptibility of 10 different antibiotics. IRPa was screened by testing the minimal inhibitory concentration of imipemem by using agar diluiion method.The susceptibility of these IRPa to the antibiotics was analysised. Three-dimensional test was used to identify the different kinds of beta lactamases from 220 strains of Pa.2.Carbarpenems hydrolytic enzyme genes and oprD2 gene were detectedamong the selected IRPa strains, PCR method was performed to detect carbapenemase genes which included GES、KPC、SPM、VIM、IMP、GIM gene and the oprD2 gene;Multiplex PCR were used to detect OXA genes and plasmid-mediated AmpC beta lactamase genes; The expression of the chromosomal AmpC beta lactamases and oprD2 genes in IRPa strains were analyzed by Real-time PCR.3.Identification and characterization of integronsIntegrase gene was detected by PCR, and the classification of integrons was performed by using restriction fragment length polymorphism.PCR was performed to detect the qacE△1-sull gene,and the gene cassetes which are located at variable region of integrons in the strains were detected to be positive.

方法1、药敏实验和三维实验收集2003~2007年临床分离的220株Pa,对这些菌株采用K-B法测定10种临床常用抗生素的药敏情况,同时采用琼脂稀释法检测亚胺培南的最低抑菌浓度(Minimal inhibitory concentration,MIC),筛选出对亚胺培南耐药的铜绿假单胞菌,并分析其对其它抗生素的药物敏感率;采用三维实验的方法分析220株Pa产β内酰胺酶的类型。2、碳青霉烯类水解酶和oprD2蛋白的检测针对鉴定的IRPa菌株,采用普通PCR方法检测具有碳青霉烯水解作用的β内酰胺酶耐药基因(GES、KPC、SPM、VIM、IMP、GIM基因)和oprD2基因,采用多重PCR的方法检测OXA型基因和质粒携带的AmpC酶基因,用荧光定量RT-PCR方法检测oprD2蛋白基因表达情况;同时对产AmpC酶的Pa(25株,含IMP耐药和敏感株)用RT-PCR方法检测AmpC酶基因的表达量情况。3。

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