RT - PCR was used to determine GK and PEPCKgene expression ( corrected by ? ? - actin ) .
用RT -PCR 檢測GK和 PEPCK mRNA表達水平的變化.
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Results CnA α, CnA ? ? could be detected by RT - PCR but no CnA ? ?.
結果RT -PCR 可檢測到CnAα 、 CnAβ,未檢測到CnAγ.
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RT - PCR was used to detect the eNOS mRNA and iNOS mRNA.
RT -PCR 分別檢測內皮細胞eNOS、iNOS基因的相對表達量.
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The expressions of bcl - x, bax and eNOS were measured by SQ - RT - PCR technique.
采用半定量逆轉錄聚合酶鏈反應(SQ-RT-PCR)法檢測內皮細胞bcl-x 、 bax以及 eNOS表達.
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Expression of TGF ? ? 1 mRNA was evaluated by RT PCR.
RT?PCR方法測定肺組織內TGF?β1的表達.
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RT - PCR confirmed that AtT - 20 cells presented an endogenous expression of H _ 4 - receptor mRNA.
RT -PCR 結果證實,在AtT-20細胞中存在組胺H4受體mRNA的內源性表達.
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Methods Reverse transcription - polymerase chain reaction ( RT - PCR ), and immunohistochemical method were used.
方法采用反轉錄 - 聚合酶鏈反應 ( RT -PCR ) 法和免疫組織化學方法.
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Methods Plasma ETA was measured quantitively by RT PCR.
方法 應用RT-PCR技術檢測外周血循環(huán)中ETA基因表達水平.
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The iNOS mRNA levels was determined by using RT - PCR .
RT -PCR 方法測定誘導型一氧化氮合酶(iNOS)mRNA水平.
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Expression of TGF ? ? 1 was evaluated by RT PCR technique.
逆轉錄聚合酶鏈反應(RT?PCR)方法測定肺組織內TGF?β1的表達.
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Then current through C 1, RT forms the return circuit preheating filament.
于是,電流通過C1 、 Rt形成回路預熱燈絲.
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This article puts forward the detailed design and realization of RT . net.
本文提出了RT. net的詳細設計和實現(xiàn)方案.
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The ECE - 1 expression was measured by RT - PCT and Western bloting.
RT -PCR 檢測轉染細胞ECE-1mRNA的表達,Westernbloting檢測細胞ECE蛋白表達情況.
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EWS - FLI 1 fusion transcripts were detected by nested RT - PCR.
EWS-FLI1融合基因檢測方法采用嵌套式RT - PCR法.
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Conclusion RT - 3 DCE was feasible in assessing EMR.
結論RT-3DCE評價二尖瓣偏心反流束體積是可行的.
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