taq dna polymerase meaning in English
taq dna聚合酶
耐热性dna聚合酶
Examples
- The y - a489 - plex multiplex pcr is feasible for using home product of taq dna polymerase
Y一a489一plex体系采用的是国产的taq酶。 - Furthermore , the home product of taq dna polymerase had the same specificity and efficiency compared to the amplitaq gold ( pe , usa ) in this study . conclusion this is the first time that the tailed primer design protocol for multiplex pcr system is used for y - str loci
初步构建了四个y一str基因座的y一a489一plex银染体系和y一a4sg一plex荧光体系:并依据dna分析技术工作组( twgdam )指南进行了应用性研究。 - Due to high sensitivity of rapd analysis to reaction conditions , main factors affecting the results including composition of the buffering system , concentrations of taq dna polymerase , primers and templates , and number of pcr cycle etc . , were examined , and conditions applicable to rapd analysis of j . curcas were determined
针对rapd标记影响因素众多、结果重复性低的特点，对rapd分析中pcr扩增的各种条件进行了梯度测试，包括反应混合液成分、 taq酶量、引物浓度、模板浓度、 pcr循环数等。 - That is to add a special fluorescence - based dna internal standard in the telomerase elongated ts primers , then do pcr amplification after a step of refinement ( hydroxybenzene / chloroform extracting , and deposited by ethanol ) . sequencing analysis of pcr product was done on 310 gene scan analysis ? . 1 . 2 dna sequencer to determine telomerase activity . notably , this method eliminated the restraining factors of taq dna polymerase , making it possible to erase the sample differences met in pcr and eradicate the annoying phenomena of pseudo negative results
在kim等开发的端粒重复扩增分析法（ trap ）的基础上进行改进，即通过对端粒酶延伸ts寡核昔酸反应产物的精制，消除了pcr扩增中抑制taq酶活性的因素，从而减少了样品之间pcr扩增上的差异和假阴性现象的发生，提高了判断样品端粒酶阴、阳性的准确率和定量的准确性。