- abbr.right 右翼，右侧
RT - PCR was used to determine GK and PEPCKgene expression ( corrected by � � - actin ) .
用RT -PCR 检测GK和 PEPCK mRNA表达水平的变化.
Results CnA α, CnA � � could be detected by RT - PCR but no CnA � �.
结果RT -PCR 可检测到CnAα 、 CnAβ,未检测到CnAγ.
RT - PCR was used to detect the eNOS mRNA and iNOS mRNA.
RT -PCR 分别检测内皮细胞eNOS、iNOS基因的相对表达量.
The expressions of bcl - x, bax and eNOS were measured by SQ - RT - PCR technique.
采用半定量逆转录聚合酶链反应(SQ-RT-PCR)法检测内皮细胞bcl-x 、 bax以及 eNOS表达.
Expression of TGF � � 1 mRNA was evaluated by RT PCR.
RT - PCR confirmed that AtT - 20 cells presented an endogenous expression of H _ 4 - receptor mRNA.
RT -PCR 结果证实,在AtT-20细胞中存在组胺H4受体mRNA的内源性表达.
Methods Reverse transcription - polymerase chain reaction ( RT - PCR ), and immunohistochemical method were used.
方法采用反转录 - 聚合酶链反应 ( RT -PCR ) 法和免疫组织化学方法.
Methods Plasma ETA was measured quantitively by RT PCR.
The iNOS mRNA levels was determined by using RT - PCR .
RT -PCR 方法测定诱导型一氧化氮合酶(iNOS)mRNA水平.
Expression of TGF � � 1 was evaluated by RT PCR technique.
Then current through C 1, RT forms the return circuit preheating filament.
于是,电流通过C1 、 Rt形成回路预热灯丝.
This article puts forward the detailed design and realization of RT . net.
The ECE - 1 expression was measured by RT - PCT and Western bloting.
RT -PCR 检测转染细胞ECE-1mRNA的表达,Westernbloting检测细胞ECE蛋白表达情况.
EWS - FLI 1 fusion transcripts were detected by nested RT - PCR.
EWS-FLI1融合基因检测方法采用嵌套式RT - PCR法.
Conclusion RT - 3 DCE was feasible in assessing EMR.