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.

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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.

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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.

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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.

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Expression of TGF ? ? 1 mRNA was evaluated by RT PCR.

RT?PCR方法测定肺组织内TGF?β1的表达.

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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.

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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.

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Methods Plasma ETA was measured quantitively by RT PCR.

方法　应用RT-PCR技术检测外周血循环中ETA基因表达水平.

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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.

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Expression of TGF ? ? 1 was evaluated by RT PCR technique.

逆转录聚合酶链反应(RT?PCR)方法测定肺组织内TGF?β1的表达.

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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.

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This article puts forward the detailed design and realization of RT . net.

本文提出了RT. net的详细设计和实现方案.

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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.

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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.

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Conclusion RT - 3 DCE was feasible in assessing EMR.

结论RT-3DCE评价二尖瓣偏心反流束体积是可行的.

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