PCR method weas used to detect 99 domesticated Paguma larvata.
对99只人工养殖的果子狸采用聚合酶链反应进行检测。
Methods RT-PCR method were used.
方法采用逆转录聚合酶链反应(RT pcr)法。
Individual genotype was detected by PCR method.
PCR方法检测个体基因型；
The P1 structure gene was amplified by PCR method.
采用PCR扩增方法获取P1结构基因。
Conclusion of PCR method can be an excellent DNA marker.
结论P CR扩增法可以获得优良的DNA分子量标准。
Using fluorescence quantitative PCR method of quantitative analysis.
采用荧光定量pcr的方法进行定量分析。
PurposeThe aim is to obtain recombinant hirudin gene using PCR method.
目的应用PCR方法获得水蛭素基因。
The PCR method were performed to determine the genotypes of aminoglycoside modifying enzymes.
用PCR法检测氨基糖苷类药物修饰酶基因。
Conclusion PCR method is better than isoenzyme analysis in differentiating An. minimus a and c.
结论对于微小按蚊a、C的鉴别，PCR方法明显优于同工酶方法。
So the PCR method was suitable for rapid and sensitive detection of human botulism borne clostridia.
因此，此P CR方法可用于快速敏感地检测引起人类肉毒中毒的梭菌。
Objective: to establish a PCR method for gene identification and genotyping of clostridial neurotoxin.
目的：建立梭菌属神经毒素基因快速鉴定和分型的PCR方法。
Objective: To study the sensitivity of PCR method for the detection of Listeria monocytogenes in food.
目的：研究PCR检测不同食品中产单核李斯特菌的灵敏度。
The PCR method verified in the research have a potentiality to detect D, f and D. p in the environment.
本研究方法具有检测环境中粉尘螨和屋尘螨的潜力。
After sequence analysis, RT PCR method was used to analyze the expression pattern in human fetal tissues.
序列分析后用RTPCR方法研究胎儿组织中的表达情况。
Objective To establish PCR method for the detection of the asymptomatic infection of Leishmania infantum.
目的建立适合检测我国婴儿利什曼原虫无症状感染的PCR方法。
Furthermore, the reaction system and program of ERIC-PCR method for the acid mineral drainage were optimized.
确定了ERIC方法用于酸性矿坑水样品时的最佳扩增体系和反应程序。
Quantitative RT PCR method were used to detect the mRNA levels of multidrug resistance gene in 32 leukemia children.
应用逆转录PCR结合同位素定量分析，对32例儿童白血病患者的多源耐药基因表达水平进行了研究。
A chlamydia psittaci were isolated from affected chickens and the PCR method for chicken chlamydiosis was established.
本研究分离了鸡源鹦鹉热衣原体，建立了鸡衣原体病PCR诊断方法。
Methods Semi-quantitative PCR method was used in this research to estimate PERV copy-number of four mini-pigs in China.
方法采用半定量pcr方法检测了我国四种小型猪内源性逆转录病毒基因的拷贝数。
Compared to the 'reference' standard (histopathology), the PCR method had a sensitivity of 83% and a specificity of 66%.
对比参考标准(组织病理学)而言，P CR方法具有83%的敏感性以及66%的特异性。
ConclusionDue to specificity on enterovirus, the RT PCR method has some value in the diagnosis of enterovirus infections.
结论该RT -PCR方法具有肠道病毒特异性，在肠道病毒感染的诊断中有一定应用价值。
The result in this paper showed that the TP-PCR method is one of rapid and convenient methods for fused gene construction.
本文研究结果表明，PCR一步法是一种快速方便的构建融合基因的方法。
It was proved that vitellogenin is synthesized in ovary and hepatopancreas in mature female shrimp through the RT-PCR method.
通过RT - P CR证实了雌虾的卵巢和肝胰腺是卵黄蛋白原的合成位点。
Conclusion the applications of combined PCR method make the amplification of long gene sequences more convenient and accurate.
结论联合pcr技术的应用使较长长度的基因序列的扩增更为方便、准确。
Methods Serological test and PCR method were used to detect 117 of 15 species of wild animals and 99 domesticated Paguma larvata.
方法对广西境内15种117只野生动物及99只人工养殖的果子狸采用聚合酶链反应和血清学方法检测其病毒核酸。
Methods: Expressions of WT1 and LRP genes were measured in 73 patients with acute leukemia and 23 normal controls by RT-PCR method.
方法：应用逆转录-聚合酶链反应(RT - pcr)法检测73例急性白血病患者及23例正常人的WT 1及LRP基因的表达。
The results of agarose gel electrophoresis and DNA sequence analysis indicated that the PCR method had high specificity and sensitivity.
结果经琼脂糖凝胶电泳和DNA序列测定证实，建立的PCR检测方法具有极高的灵敏度和较好的特异性。
All the 6 genotypes (9 strains) of measles virus showed DNA positive strand, it means this RT-PCR method is sensitive for measles viruses.
结果9株6种基因型麻疹病毒RT PCR均呈现阳性条带，说明本研究采用的RT PCR方法敏感。
Methods PCR method was used to detect micro-deletion in AZF gene in 62 oligospermatism and azoospermatism patients and 20 normal male controls.
方法 对62例无精症、少精症患者及20例正常男性采用多重聚合酶链反应法进行AZF区基因微缺失检测。
Methods PCR method was used to detect micro-deletion in AZF gene in 62 oligospermatism and azoospermatism patients and 20 normal male controls.
方法 对62例无精症、少精症患者及20例正常男性采用多重聚合酶链反应法进行AZF区基因微缺失检测。
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