Fast detection of genetic information by an optimized PCR in an interchangeable chip.
KAUST DepartmentComputational Bioscience Research Center (CBRC)
Physical Science and Engineering (PSE) Division
KAUST Grant NumberSA-C0040/UK-C0016
Online Publication Date2011-10-06
Print Publication Date2012-02
Permanent link to this recordhttp://hdl.handle.net/10754/303136
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AbstractIn this paper, we report the construction of a polymerase chain reaction (PCR) device for fast amplification and detection of DNA. This device consists of an interchangeable PCR chamber, a temperature control component as well as an optical detection system. The DNA amplification happens on an interchangeable chip with the volumes as low as 1.25 μl, while the heating and cooling rate was as fast as 12.7°C/second ensuring that the total time needed of only 25 min to complete the 35 cycle PCR amplification. An optimized PCR with two-temperature approach for denaturing and annealing (Td and Ta) of DNA was also formulated with the PCR chip, with which the amplification of male-specific sex determining region Y (SRY) gene marker by utilizing raw saliva was successfully achieved and the genetic identification was in-situ detected right after PCR by the optical detection system.
CitationWu J, Kodzius R, Xiao K, Qin J, Wen W (2011) Fast detection of genetic information by an optimized PCR in an interchangeable chip. Biomed Microdevices 14: 179-186. doi:10.1007/s10544-011-9595-6.
SponsorsAward No. SA-C0040/UK-C0016 made by King Abdullah University of Science and Technology (KAUST); Hong Kong Research Grants Council Grant No. HKUST 603608
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