restriction enzyme analysis的意思

restriction enzyme analysis中文翻譯：

限制性酶切分析，限制性內切酶分析

相似詞語短語

restriction enzyme───[遺]限制性內切酶；[遺]限制酶

restriction───n.限制；約束；束縛

enzyme───n.[生化]酶

analysis───n.分析；分解；驗定

restriction orifice───節流孔板

assimilatory enzyme───同化酶

conjugated enzyme───綴合酶；結合酶類；[生化]結合酶

effector enzyme───效應酶

caloric restriction───[醫]熱限制

雙語使用場景

Results Restriction enzyme analysis and DNA sequence analysis showed that PTEN gene was cloned and the eukaryotic expression vector was constructed successfully.───結果酶切和測序證實PTEN基因克隆和真核表達載體構建成功。

were prepared by alkali lysis and purified with polyethylene glycol 8000. Restriction enzyme analysis show that both genes are well-constructed suitable for transgenic animal experiment.───限制性酶切圖譜分析證實這兩個基因的結構是完整的，符合轉基因實驗要求。

sheep and goat derived materials were positive in mixed feed powders of level test by PCR and restriction enzyme analysis.───CR檢測和酶切鑒定結果表明，在水平測試的混合飼料粉中可檢出牛源、羊源性成分。

Results The three results of restriction enzyme analysis are coincident completely, and the method is more precise than RT-PCR.───結果限制性內切酶分析法的三次檢測結果完全一致，較RT-PCR法的檢測結果更精確。

Finally a recombinant plasmid named pcNcSRS2, which was identified by PCR, restriction enzyme analysis and sequencing, was obtained.───經PCR鑒定、限制性內切酶分析和克隆片段序列測定、比較，證實了重組質粒的正確性。

Polymerase chain reaction and restriction enzyme analysis of human cytomegalovirus infection in pregnant women and neonates───孕婦及新生兒巨細胞病毒感染的聚合酶鏈反應及限制酶分析

英語使用場景

Plasmid DNAs were prepared by alkali lysis and purified with polyethylene glycol 8000. Restriction enzyme analysis show that both genes are well-constructed suitable for transgenic animal experiment.

The bovine, sheep and goat derived materials were positive in mixed feed powders of level test by PCR and restriction enzyme analysis.

The recombinant plasmid pcDNA3 F was stable within the host stain ZJ111 in vitro and in vivo as shown by restriction enzyme analysis and PCR identification of the F gene.

Methods: The serum samples were collected from 56 patients with morbilliform maculopapular eruption. The target DNA of CBV was detected by RT-PCR and restriction enzyme analysis.

Finally a recombinant plasmid named pcNcSRS2, which was identified by PCR, restriction enzyme analysis and sequencing, was obtained.

Subcloning and comparative restriction enzyme analysis were carried out with the replication origin from tne integrated F' plasmid and that from the autonomous F plasmid.

Results Restriction enzyme analysis and DNA sequence analysis showed that PTEN gene was cloned and the eukaryotic expression vector was constructed successfully.