taq怎么读

taq怎么读：taqt?k

TAQ 双语例句

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.

实验发现，6种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、亚甲基富勒烯二膦酸四乙酯、亚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对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.

本文介绍了Taq DNA聚合酶的结构与功能改造的研究现状，并展望了Taq DNA聚合酶在医药领域的应用前景。

3. The interaction of colloidal gold with?Taq?DNA polymerase was investigated in this study.

本文研究了胶体金与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.

结果 Taq I位点等位基因在2组间分布差异有统计学意义。

5. The prepared methods of recombinant?Taq?DNA polymerase in our laboratory are simple and rapidly.

结论该方法制备可用于PCR的Taq酶具有快速简便的优点。

6. This experimentation will establish the expression vector of?Taq?DNA polymerase gene.

本实验将构建Taq DNA聚合酶的基因表达载体。

7. Objective To compare two methods of preparing purified?Taq?DNA polymerase in order to provide experimental enzyme for polymerase chain reaction.

目的比较2种制备纯化Taq DNA聚合酶的方法，为PCR提供实验用酶。

8. The result is that:1、the fitting concentrations for the?Taq?DNA polymerase, 25mMol?

试验结果：1、优化的猪源性成分PCR反应体系中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.

建立荧光定量PCR体系以准确灵敏的鉴定小麦黑穗菌(Tilletia controversa Kühn，TCK)根据筛选的TCK独有差异基因片段(1322bp)设计特异性引物对CQUTCK4/CQUTCK5和TaqMan探针CQUP1，建立SYBR GreenⅠ荧光染料法和Taq Man水解探针法定量PCR检测体系，并对体系进行优化。

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.

研究用高保贞Taq酶通过PCR方法从正常人的基因组DNA中扩增出1182bp的人胰岛素原基因，运用TA克隆的方法将扩增片段插入PGEM-T-easy载体中，在Genebank中全序列分析表明扩增出的hINS与其中一个发表序列完全吻合，而与另外的一个发表序列同源性为99％，不同的碱基其中一处是位于内含子，其它三处位于等位多变点，这种碱基的差别可能与取样的人种有关。