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.
它们共同控制着基因的转录。
植物基因的转录调控是以组合控制方式进行的。
The transcription of plant genes is regulated in the way of combination control.
转录调控是基因表达调控的重要方式。
Transcriptional control is an important way of regulating of gene expression.
目的构建人P 58.1基因的逆转录病毒表达载体并探讨该基因在淋巴细胞中的表达。
To construct the retroviral expression vector of Human P58.1 gene and study its expression in lymphocytes.
LT基因的表达调控主要是在转录水平上。
The expression of LT gene is primarily controlled at the level of transcription.
在转录水平，发现了新的异常剪接基因。
On transcriptional level, no foregone alternative splicing event was found.
逆转录酶基因耐药性突变的发生率是38.9%（14/36）。
The mutation rate of resistance to reverse transcriptase was 38.9 %(14/36).
RT-PCR结果显示目的基因已被成功转录。
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。
The RT-PCR result showed that purpose gene was succeed in transcribing.
应用推荐