VARIABILITY OF THE RANDOM AMPLIFIED POLYMORPHIC DNA ASSAY AMONG THERMAL CYCLERS, AND EFFECTS OF PRIMER AND DNA CONCENTRATION

被引:138
作者
MACPHERSON, JM
ECKSTEIN, PE
SCOLES, GJ
GAJADHAR, AA
机构
[1] AGR CANADA,HLTH ANIM LAB,116 VET RD,SASKATOON S7N 2R3,SASKATCHEWAN,CANADA
[2] UNIV SASKATCHEWAN,COLL AGR,DEPT CROP SCI & PLANT ECOL,SASKATOON S7N 0W0,SASKATCHEWAN,CANADA
关键词
PCR; RAPD; DNA CONCENTRATION; PRIMER CONCENTRATION; THERMAL CYCLERS; DNA FINGERPRINTS;
D O I
10.1006/mcpr.1993.1043
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The reproducibility of the generation of random amplified polymorphic DNA fragments from three commonly used thermal cyclers was determined using identical assay conditions. In all cases, different results were obtained from the three instruments. Variation in the length of the primer (20 nt or 10 nt) did not have any effect on the reproducibility of the assays from the three machines tested. A DNA concentration of 1 ng generated poorly staining DNA fragments whereas concentrations between 10 ng and 100 ng gave similar banding patterns when using the same thermal cycler. Low concentrations of primer (0.05 μM) did not produce any detectable DNA fragments. Increased primer concentrations of 0.25 μM or higher generated intensely staining DNA fragments, and concentrations above 0.5 μM did not improve the clarity of the banding patterns but did direct the synthesis of increasing amounts of very short DNA fragments. Surprisingly, the 20 nt-long primer was able to direct the synthesis of more DNA fragments than a primer of only 10 nt long. © 1993 Academic Press, Limited.
引用
收藏
页码:293 / 299
页数:7
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