逆转录-实时荧光定量聚合酶链反应,Reverse transcription-Real time Quantitative polymerase chain reaction
real-time fluorescence relative quantitative RT-PCR实时荧光定量-逆转录-聚合酶链反应
3)real time quantitative RT-PCR实时荧光定量逆转录聚合酶链反应
1.Methods Adult Wistar rats were exposed to hypobaric hypoxic environment for 2 hours following which the expression of AngⅡwere observed at 3 hours,24 hours,3 days,7 days and 14 days with real time quantitative RT-PCR and Western-blotting,respectively.L-1O2)2h后,分别在3h、24h、3d、7d和14d,通过实时荧光定量逆转录聚合酶链反应、蛋白免疫印迹法检测AngⅡ在视网膜中的表达情况。
4)real-time quantitative reverse transcription polymerase chain reaction实时荧光定量逆转录-聚合酶链反应
1.The COL3A1 mRNA was measured by real-time quantitative reverse transcription polymerase chain reaction(RT-PCR).方法应用基因芯片技术和实时荧光定量逆转录-聚合酶链反应(RT-PCR)技术,检测Ⅲ型胶原α链在不同舌苔中的表达水平。
5)Real-time RTpolymerase chain reaction实时荧光定量逆转录聚合酶链式反应
6)Real-time fluorescent quantitative reverse transcriptase polymerase chain reaction实时荧光定量逆转录聚合酶链反应
1.METHODS: Real-time fluorescent quantitative reverse transcriptase polymerase chain reaction (RT-PCR) was used to detect the level of hPMS2 mRNA respectively in 41 cases of gastric cancer and 37 cancer-adjacent mucosa samples of atrophic gastritis and 25 cases of chronic atrophic gastritis and 20 cases of chronic superf icial gas-tritis.方法:应用实时荧光定量逆转录聚合酶链反应(RT-PCR)技术对41例胃癌患者的癌组织、37例癌旁萎缩性胃炎组织、25例慢性萎缩性胃炎组织及20例慢性浅表性胃炎组织中hPMS2 mRNA进行定量检测,以三磷酸甘油醛脱氢酶基因(hGAPDH)为内参照。
延伸阅读

聚合酶链反应聚合酶链反应polymerase chain reaction,PCR 是用特异性寡核苷酸引物在DNA聚合酶的作用下对靶DNA序列进行大量扩增的分子生物学方法。PCR技术中以在短时间内把极其微量的特定DNA(或RNA)片断大量增扩,达到用常规方法就可以检测的水平。临床用来确定一些疾病的病原体,因其假阳性率较高,故应谨慎使用。