taq怎麽讀：taqt?k
TAQ 雙語例句
It was discovered that trimalonic acid C60、fullerol、dimalonic[60]fullerene hydrolysate、tetraethyl methano[60]fullerenediphosphonate、methano[60]fullerenediphosphonic acid and dimalonic acid C60 exhibited different inhibitory effects on?Taq?DNA polymerase.
實驗發現，6種富勒烯衍生物三丙二酸富勒烯、富勒醇、富勒烯丙二酸水解物、亞甲基富勒烯二膦酸四乙酯、亞甲基富勒烯二膦酸四乙酯的完全水解物和二丙二酸富勒烯對Taq DNA聚合酶存在不同程度的抑制作用。
2. Current advance of?Taq?DNA polymerase improvement and application in medicine has been discussed in this paper.
本文介紹了Taq DNA聚合酶的結構與功能改造的研究現狀，並展望了Taq DNA聚合酶在醫藥領域的應用前景。
3. The interaction of colloidal gold with?Taq?DNA polymerase was investigated in this study.
本文研究了膠體金與Taq DNA聚合酶的相互作用。
4. Results Allele frequencies of?Taq?I polymorphism had significant differences between the two groups.
結果 Taq I位點等位基因在2組間分布差異有統計學意義。
5. The prepared methods of recombinant?Taq?DNA polymerase in our laboratory are simple and rapidly.
結論該方法制備可用於PCR的Taq酶具有快速簡便的優點。
6. This experimentation will establish the expression vector of?Taq?DNA polymerase gene.
本實驗將構建Taq DNA聚合酶的基因表達載體。
7. Objective To compare two methods of preparing purified?Taq?DNA polymerase in order to provide experimental enzyme for polymerase chain reaction.
目的比較2種制備純化Taq DNA聚合酶的方法，為PCR提供實驗用酶。
8. The result is that:1、the fitting concentrations for the?Taq?DNA polymerase, 25mMol?
試驗結果：1、優化的豬源性成分PCR反應體系中Taq DNA聚合酶、25mMol？
9. To detection of Tilletia controversa Kühn sensitively and accurately, real-time PCR systems were developed. The species-specific primer pair CQUTCK4/CQUTCK5 and probe CQUP1 were designed based on a selected specific fragment (1322 bp) specific for TCK, and the SYBR Green I and?TaqMan quantitative PCR detection systems were established with optimized reaction conditions.
建立熒光定量PCR體系以準確靈敏的鑒定小麥黑穗菌(Tilletia controversa Kühn，TCK)根據篩選的TCK獨有差異基因片段(1322bp)設計特異性引物對CQUTCK4/CQUTCK5和TaqMan探針CQUP1，建立SYBR GreenⅠ熒光染料法和Taq Man水解探針法定量PCR檢測體系，並對體系進行優化。
10. This study is focused on the feasibility of producing human insulin in the animal mammary gland. In this study, we amplified the 1182 bp genome DNA of human proinsulin by pyrobest?Taq?PCR from human genome.
研究用高保貞Taq酶通過PCR方法從正常人的基因組DNA中擴增出1182bp的人胰島素原基因，運用TA克隆的方法將擴增片段插入PGEM-T-easy載體中，在Genebank中全序列分析表明擴增出的hINS與其中壹個發表序列完全吻合，而與另外的壹個發表序列同源性為99％，不同的堿基其中壹處是位於內含子，其它三處位於等位多變點，這種堿基的差別可能與取樣的人種有關。