Polymerase chain reaction in polymeric microchips:: DNA amplification in less than 240 seconds

被引:225
|
作者
Giordano, BC
Ferrance, J
Swedberg, S
Hühmer, AFR
Landers, JP
机构
[1] Univ Virginia, Dept Chem, Charlottesville, VA 22901 USA
[2] Univ Virginia, Dept Pathol, Charlottesville, VA 22901 USA
[3] Agilent Technol, Palo Alto, CA USA
[4] ThermoFinnigan, San Jose, CA USA
关键词
polymerase chain reaction; thermocycling; PCR fragment; capillary electrophoresis; polyimide; polyethylene glycol; thermocouple; microchips;
D O I
10.1006/abio.2000.4974
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
There is much interest in developing methods amenable to amplifying nucleic acids by the polymerase chain reaction (PCR) in small volumes in microfabricated devices. The use of infrared-mediated temperature control to accurately thermocycle microliter volumes in microchips fabricated from polyimide is demonstrated. Amplification of a 500-base-pair fragment of h-phage DNA was achieved in a 1.7-mul chamber containing a thermocouple that allowed for accurate control of temperature, While previous work showed that Tag polymerase was inactivated when in direct contact with the thermocouple, this was circumvented with the polyimide chip by the addition of polyethylene glycol as a buffer additive, This, consequently, allowed for adequate amounts of PCR product to be observed after only 15 cycles, with a total time for amplification of 240 s. (C) 2001 Academic Press.
引用
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页码:124 / 132
页数:9
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