taq

Direct DNA Sequencing of Polymerase Chain Reaction Products With Taq DNA Polymerase

利用taq DNA聚合酶对PCR产物直接进行顺序分析

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The affinity of Taq pol binding with DNA T-P decreased when the number of mismatched bases increased.

引物末端一个至多个的碱基错配影响了Taq聚合酶（Taq pol）和DNA模板-引物（DNA T-P）的结合，随错配碱基个数增多Taq pol和DNA的亲和力下降。

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High content of protein, phenol, tannin, pigment and polysaccharide in plant tissues usually affect the activity of Taq DNA polymerase and Lead to failure of PCR reaction.

植物体内所含的蛋白质、单宁、酚类、多糖及色素等次生代谢物质影响taq DNA聚合酶的活性，是导致PCR扩增反应失败的主要因素。

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One of the mechanisms causing gene mutation might be to change of the Taq DNA polymerase conformation. It interfers with the enzyme-substrate-dNTP binding site and further causes replication mismatch.

这一实验结果也说明了稀土是一种诱变剂，引起基因突变的机制之一可能是改变taq DNA聚合酶的立体构象，干扰了酶与底物dNTP结合位点，从而引起复制错配。

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[ METHOD] Different levels on concentration of DNA template, primer, dNTP mixture and Taq DNA polymerase and annealing temperature were set in this experimentation. All factor influence for SRAP-PCR in peanut genome was investigated.

【方法】对模板DNA、引物、dNTP mixture、taq DNA聚合酶浓度及退火温度设置不同梯度，研究各因素对PCR结果的影响；

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Moreover, the concentrations of Mg2+, dNTP and Taq DNA polymerase in allele-specific PCR were higher than that in conventional PCR.

在等位基因特异PCR中，Mg2+、dNTP及taq DNA聚合酶的用量均大于普通PCR。

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Rapid Purification of High-activity Recombinant Taq DNA Polymerase Using Freezing-thawing Method

以冻融法快速纯化高活力基因工程taq DNA聚合酶

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The DNA repair techniques with Taq DNA polymerase can greatly enhance the success rate of STR genotyping for high degrade samples, which is suitable for the STR genotyping of high degrade samples. 3.

使用taq DNA聚合酶修复技术可以极大地提高高度降解检材STR分型的成功率，适合高度降解检材STR分型的应用。

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This study concentrated on extracting and purification of Taq and Pfu DNA polymerase in the recombinant strains.

本文主要研究从重组工程菌中分别提取Pfu DNA聚合酶及taq DNA聚合酶。

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With genome DNA as template, three upstream primers ( R1 、 R2 、 R3) targeting point mutation of K-ras oncogene codon 12 and common downstream primer ( R4) were added respectively. PCR was employed to amplify corresponding fragment with Taq DNA polymerase.

以基因组DNA为模板，分别加入针对K-ras第12密码子的三种主要突变方式设计的PCR上游引物R1、R2、R3和共同的下游引物R4，在taq DNA聚合酶作用下扩增相应片段。

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Optimization of Preparation Techniques of Taq DNA Polymerase

taq DNA聚合酶制备技术的优化

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Methods Investigations were conducted in 620 students within 4 days before examination with the Cognitive Test Anxiety Scale ( CTAS), Test Anxiety Scale ( TAS) and Test Anxiety Questionnaire ( TAQ) respectively and correlations analyzed.

方法对620名初中生采用《认知考试焦虑量表》、《考试焦虑量表》、《考试焦虑问卷》分别于期末考试前4d进行测试，并进行相关性分析。

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Separation and Purification of Taq DNA Polymerase in E. coli

大肠杆菌表达重组taq DNA聚合酶的分离和纯化

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Although the commercial production of Taq DNA polymerase has come true for many years and a lot of technique improvement has been made, the activity ratio of the enzyme preparation is not high, some methods of procedure too complicated, or the production cost is high.

虽然taq DNA聚合酶已经商品化生产多年，制备方法较多，但是目前一些方法生产的酶制剂比活性不高，而一些方法又过于繁琐，增加生产成本。

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In order to establish the optimized SSR detection system, the concentrations of DNA, Mg~ ( 2+), Taq DNA polymerase, dNTPs, and the annealing temperature were optimized for SSR-PCR reaction.

为建立适宜的SSR反应体系，对影响SSR-PCR扩增的模板DNA浓度、Mg~（2+）的用量、taq DNA聚合酶浓度、dNTPs浓度、退火温度等因素进行了优化。

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After Taq DNA polymerase had been isolated and purified from the thermophilic bacteria ( Thermus aquatics) in aquatic habitat by Randall K. Saiki and his colleagues in 1988, it was widely used in PCR techniques.

1988年，Randall K.Saiki等[1.2]从水生栖热菌（Thermus aquatics）中分离纯化到了taq DNA聚合酶，之后它广泛应用于PCR技术。

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Methods Slides of metaphase chromosome were examined by the method of PCR in situ. And PCR reactions without Taq DNA polymerase, primer and bio 11 dUTP were set up as control groups.

方法应用原位PCR的方法对豫医无毛小鼠中期染色体标本的无毛基因进行检测，并设立PCR反应液中无taq DNA聚合酶、无引物、无bio-11-dUTP等进行多组对照。

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Results and conclusion: Taq DNA Polymerase labeling method is as efficient as Klenow fragment random primer DNA labeling system.

结果与结论：Taq酶标记法和大肠杆菌Klenow片段随机引物延伸标记法同样有较好的标记效果，且随机引物或特定引物作为延伸引物均可以合成足够有效的探针。

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The two systems were easy to optimize and using domestic Taq can obtain satisfied amplification results.

本实验构建的两个复合扩增体系条件易于优化，采用国产Taq酶进行扩增，即可得到满意的扩增产物和分型结果。

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Taq DNA polymerase is an ideal enzyme for DNA sequencing because it's fast, highly processive and active over a broad range of temperature.

taq DNA聚合酶具有反应速度快、温度作用范围广及良好的续进性等特点，可视为一种理想的DNA顺序分析酶。

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Taq DNA polymerase is a kind of the highly heat-stable DNA polymerase, that was isolated from thermophilic bacterium Thermus aquaticus. Because of its high thermostability, high specificity, sensitivity and other excellent features, Taq DNA polymerase is widely used in the PCR amplification.

taq DNA聚合酶是一种来源于嗜热菌Thermus aquaticus的高度热稳定的DNA聚合酶，并以其耐高温、较高的特异性、灵敏度等优良特性被广泛应用在PCR扩增中。

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Using the thermostable ability of Taq DNA polymerase, the protein was immerged in a 75 ℃ water-bath for 1h, and then obtained by the method of ammonium sulfate precipitation.

利用Taq酶的热稳定性，将破胞液在75℃水浴1h，然后用硫酸铵沉淀法获得纯化的表达蛋白。

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Concentration of primer, magnesium chloride, dNTP, template DNA, Taq DNA polymerase and annealing temperature in PCR and the quantity of PCR product and endonuclease and digesting time in digestion process affect the profiles of the whole experiment.

PCR反应体系中不同模板含量、引物浓度、taq DNA聚合酶用量、dNTP浓度、Mg2+浓度、退火温度和酶切体系中PCR产物量、内切酶量、酶切时间等对反应结果均有不同程度的影响。

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General Taq DNA polymerase amplified long DNA fragments of Helicobacter pylori urease

普通taq DNA聚合酶扩增幽门螺杆菌尿素酶基因长片段

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The total DNAs from 3 species of plants and 2 species of animals were amplified by RAPD ( random amplified polymorphic DNA) using 10 RAPD 10 nt primers and 3 different commercial Taq DNA polymerases, respectively.

随机选用了10条RAPD引物，采用3种商品taq DNA聚合酶体系，以5个不同物种的动植物总DNA为模板，进行RAPD扩增。

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Direct Amplification of Target Sequences by Taq DNA Polymerise Using Double-stranded Rna as Templates

利用taq DNA聚合酶直接从双链RNA模板中扩增靶序列

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Study on some problems of TAQ in high grade office buildings in Beijing

北京市一些高级办公大楼室内空气质量问题探讨

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Optimization of Recombinant Taq DNA Polymerase Expression in E.coli

重组taq DNA聚合酶在大肠杆菌中表达条件的优化

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Methods: The circled TA plasmid was digested and linearized with restriction endonuclease. The ends of the plasmid were repaired and made blunt with Klenow Fragment. A single T was added respectively to the 5 ′ ends of the vector with Taq DNA polymerase.

方法：将环化质粒以限制性内切酶消化成线性后，以Klenow大片段将末端补平，再用taq DNA聚合酶在线性载体的两个5′末端各加上一个非配对的T。

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Study on the Functional Domain of Taq DNA Polymerase

taq DNA聚合酶功能区域的定位

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