Polymerase chain reaction (PCR).
聚合酶链反应。
Results Effective PCR condition was found;
结果获得适合的PCR条件；
Prove RT-PCR detection method is peculiar very high.
结果表明RT-PCR检测方法有很好的特异性。
The expression of multiple gene was evaluated by DD-PCR.
荧光基因差异显示分析法检测多基因表达水平。
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。
Objective To study the diagnostic value of PCR in tuberculosis.
目的探讨PCR法对结核病的诊断价值。
The RT-PCR result showed that purpose gene was succeed in transcribing.
RT-PCR结果显示目的基因已被成功转录。
Methods Narcotics test and 4-pair-primer-pcr are both done in traditional way.
方法毒力测定和4对引物pcr按常规方法进行。
It was thought that molecular test technology based on PCR must be efficient m...
可以认为，以PCR为基础的分子检测技术将是对食品微生态系进行研究的有效手段。
Conclusion it is a general and effective method to clone PCR products with T-vectors.
结论t -载体法是克隆pcr产物通用而有效的方法。
Objective: To discuss the value of aspergillus PCR in organ transplant infection control.
目的：探讨PCR检测曲霉菌在器官移植感染控制中的应用价值。
PCR-primer design is the most important step in polymerase chain reaction (PCR) technique.
引物设计是P CR技术中最重要的一环。
Last, we analysised the expression of IFRG gene in seven different rabbit tissue by RT-PCR.
通过RT - PCR初步分析IF RG基因在兔七种不同组织中的表达情况。
The principle, method and application of Polymerase Chain Reaction (PCR) was introduced in this paper.
介绍了分子生物学前沿技术聚合酶链式反应(PCR)的原理、方法及应用。
Various reverse transcriptase–polymerase chain reaction (RT–PCR) methods are available but are of variable sensitivity.
有各种逆转录酶聚合酶链反应(扩增核糖核酸基因组RT–PCR)检测试验方法，但灵敏度各不相同。
Various reverse transcriptase–polymerase chain reaction (RT–PCR) methods are available but are of variable sensitivity.
有各种逆转录酶聚合酶链反应(扩增核糖核酸基因组RT–PCR)检测试验方法，但灵敏度各不相同。
应用推荐