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Capillary electrophoresis as a tool for optimization of multiplex PCR reactions
J M Butler1, C M Ruitberg, P M Vallone
1National Institute of Standards and Technology, Biotechnology Division, Gaithersburg, MD 20899, USA. john.butler@nist.gov
Abstract:
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.
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