Performance evaluation of thermal cyclers for PCR in a rapid cycling condition

• Published in: BioTechniques Vol. 44; no. 4; pp. 495 - 505
• Main Authors: Ho Kim, Young, Yang, Inchul, Bae, Young-Seuk, Park, Sang-Ryoul
• Format: Journal Article
• Language: English
• Published: Natick, MA Future Science Ltd 01.04.2008; Eaton; Taylor & Francis Group
• Subjects: Biological and medical sciences; Diverse techniques; DNA - analysis; Equipment Design; Female; Fundamental and applied biological sciences. Psychology; Humans; Microchemistry - instrumentation; Microchemistry - methods; Microchemistry - standards; Molecular and cellular biology; Placenta - chemistry; Polymerase Chain Reaction - instrumentation; Polymerase Chain Reaction - methods; Polymerase Chain Reaction - standards; Pregnancy; Temperature; Templates, Genetic; Time Factors; Performance evaluation; Polymerase chain reaction
• ISSN: 0736-6205; 1940-9818
• DOI: 10.2144/000112705

The performance of thermal cyclers for polymerase chain reactions (PCR) is of great concern in terms of the reliability of PCR-based assays, particularly when rapid cycling conditions are applied to small volume reactions. In this work, the precision of the temperature controls during rapid thermal cycling was measured in 19 commercial thermal cyclers of 8 different models. The temperatures of test solutions in specific locations in each thermal block were simultaneously monitored at 1 s intervals during thermal cycling. A temperature-sensitive multiplex PCR was run in parallel to assess undesirable PCR results caused by poor temperature control. Under the given conditions (20 s of annealing time and 20 µL reaction volume), a majority of the tested instruments showed prominent curving, undershooting, and/or overshooting in their temperature profiles, which substantially influenced the results of the temperature-sensitive multiplex PCR. Variations between wells were also observed in most instruments. It is strongly hoped that these problems will be addressed by manufacturers and that they will make substantial improvements in the precision and efficiency of thermal cyclers. In the meantime, users of thermal cyclers might be able to avoid unexpected poor outcomes of sensitive PCR-based assays by designing their PCR protocols with these findings in mind.