Methods Polymerase chain reaction ( PCR ) connected with reverse dot blot ( RDB ) were performed.
方法采用多聚酶鏈反應(yīng) ( PCR ) 結(jié)合反向斑點(diǎn)雜交 ( RDB ) 技術(shù).
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Methods Reverse transcription - polymerase chain reaction ( RT - PCR ), and immunohistochemical method were used.
方法采用反轉(zhuǎn)錄 - 聚合酶鏈反應(yīng) ( RT -PCR ) 法和免疫組織化學(xué)方法.
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DNA molecule to RNA polymerase binds, initiating the transcription of RNA.
一種rna模板上的dna形成的聚合酶, 尤其在逆轉(zhuǎn)錄酶病毒中發(fā)現(xiàn).
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Inhibits platelet aggregation. DNA polymerase inhibitor. Shows antifungal activity.
抑制血小板聚集. DNA聚合酶抑制劑. 顯示抗真菌活性.
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The sex of embryos were determined with PCR ( Polymerase chain reaction ) technique.
胚胎的性別鑒定采用多聚酶鏈?zhǔn)椒磻?yīng) ( PCR ) 技術(shù).
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Researchers believe that the bird virus polymerase allows for faster replication, and thus more aggressive.
研究人員認(rèn)為,禽流感病毒聚合酶允許更快的復(fù)制, 從而更加積極.
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Objective To develop a novel multiplex polymerase chain reaction ( PCR ) to detect multidrug - resistant Acinetobacter baumannii.
目的建立一種適于臨床微生物實(shí)驗(yàn)室快速檢測(cè)多耐藥 鮑曼 不動(dòng)桿菌基因的多重PCR方法.
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TLR 4 mRNA in KCs was determined by the reverse transcription polymerase chain reaction ( RT - PCR )
用逆轉(zhuǎn)錄多聚酶聯(lián)反應(yīng) ( RT -PCR ) 測(cè)定KCs中TLR4mRNA的表達(dá).
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The expression of TLR 4, MD - 2 mRNA were assayed by reverse transcriptase polymerase chain reaction ( RT - PCR ).
逆轉(zhuǎn)錄聚合酶鏈反應(yīng) ( RT -PCR ) 檢測(cè)各組細(xì)胞TLR4和MD-2mRNA的表達(dá).
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Objective To establish DNA typing for HLA - DR antigens polymerase chain reaction with sequence - specific primers ( PCR - SSP ).
目的采用順序特異引物聚合酶鏈反應(yīng) ( PCR -SSP ) 建立人類白細(xì)胞抗原DR位點(diǎn)的DNA分型方法.
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Objective To discuss the feasibility and superiority of diagnosis of acanthamoeba Keratitis using polymerase chain reaction.
目的探討聚合酶鏈反應(yīng)(PCR)技術(shù)臨床應(yīng)用于棘阿米巴角膜炎診斷的可行性及優(yōu)越性.
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The gene expression of ET - 1、 ETAR 、 ETBR and ECE was evaluated by semi - quantitative reverse transcription polymerase chain response ( RT - PCR ).
采用半定量逆轉(zhuǎn)錄多聚酶鏈反應(yīng) ( RT -PCR ) 檢測(cè)局部?jī)?nèi)皮素系統(tǒng)ET -1 、ETAR、ETBR及ECE的基因表達(dá).
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Objective To develop a quantitative real - time polymerase chain reaction ( PCR ) for detecting Bartonella henselae.
目的采用新型TaqMan -MGB 探針建立檢測(cè)漢賽巴通體的實(shí)時(shí)熒光定量PCR方法.
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Semi - quantitative reverse transcription - polymerase chain reaction ( RT - PCR ) was used to detect the level of MMP - 12 mRNA expression.
以 半定量 RT -PCR 法檢測(cè)MMP -12 mRNA表達(dá)水平.
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It was validated the extracted DNA could meet the need of polymerase chain reaction ( PCR ).
涂漬的芯片所提取出的DNA能夠滿足聚合 酶 鏈反應(yīng)的需要.
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