Meunier J R, Grimont P A
Institut Pasteur, Unité des Enterobactéries, INSERM-U.199, Paris, France.
Res Microbiol. 1993 Jun;144(5):373-9. doi: 10.1016/0923-2508(93)90194-7.
The reproducibility of random amplified polymorphic DNA (RAPD) was tested using two different thermal cyclers and three brands of Taq DNA polymerase. Three different oligonucleotides were used to obtain patterns of amplified fragments from three DNA samples (Escherichia coli, Bacillus subtilis, and Thermococcus littoralis). Experiments were repeated three to six times. Apart from the expected between-oligonucleotide and between-DNA variations, between-thermal cycler and between-DNA polymerase variations were observed. Within the DNA-oligonucleotide-DNA-polymerase-thermal cycler, reproducibility was excellent when the thermal cycler equipped with the best temperature regulation was used, but was not as good with another brand of thermal cycler.
使用两种不同的热循环仪和三个品牌的Taq DNA聚合酶对随机扩增多态性DNA(RAPD)的可重复性进行了测试。使用三种不同的寡核苷酸从三个DNA样本(大肠杆菌、枯草芽孢杆菌和嗜热栖热菌)中获得扩增片段模式。实验重复进行了三到六次。除了预期的寡核苷酸间和DNA间变异外,还观察到了热循环仪间和DNA聚合酶间的变异。在DNA-寡核苷酸-DNA-聚合酶-热循环仪体系中,当使用配备最佳温度调节功能的热循环仪时,可重复性极佳,但使用另一个品牌的热循环仪时,可重复性则没那么好。