Capillary electrophoresis as a tool for optimization of multiplex PCR reactions

被引:0
|
作者
J. M. Butler
Christian M. Ruitberg
Peter M. Vallone
机构
[1] National Institute of Standards and Technology,
[2] Biotechnology Division,undefined
[3] 100 Bureau Drive,undefined
[4] Mail Stop 8311,undefined
[5] Gaithersburg,undefined
[6] MD 20899,undefined
[7] USA e-mail: john.butler@nist.gov,undefined
来源
Fresenius' Journal of Analytical Chemistry | 2001年 / 369卷
关键词
Polymerase Chain Reaction; Electrophoresis; Thermal Cycling; Optimization Process; Capillary Electrophoresis;
D O I
暂无
中图分类号
学科分类号
摘要
Copying multiple regions of a DNA molecule is routinely performed today using the polymerase chain reaction (PCR) in a process commonly referred to as multiplex PCR. The development of a multiplex PCR reaction involves designing primer sets and examining various combinations of those primer sets and different reaction components and/or thermal cycling conditions. The process of optimizing a multiplex PCR reaction in order to obtain a well-balanced set of amplicons can be time-consuming and labor-intensive. The rapid separation and quantitation capabilities of capillary electrophoresis make it an efficient technique to help in the multiplex PCR optimization process.
引用
收藏
页码:200 / 205
页数:5
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