Yu LiuChen LiZhi LiSamuel D.H. ChanDaisuke EtoWarren WuYanping ZhangRing‐Ling ChienHenry G. WadaMichael GreensteinShinji Satomura
Electrophoresis 2016, 37, 545–552. DOI: 10.1002/elps.201500298 Quantitative polymerase chain reaction (qPCR) and capillary electrophoresis (CE) were integrated into a microfluidic chip that was designed to achieve real-time amplicon sampling, separation, and quantitation without requiring various probes. A novel channel design and PCR-CE synchronization scheme allows the overlapped execution of PCR and CE, minimizing the time required for CE analysis after each PCR cycle. The performance of the on-chip qPCRCE method was demonstrated using model assay protocols to detect phiX174 bacteriophage and E. coli genomic DNA. By combining the separation capability of CE and the amplification power of PCR assay, this method is expected to find applications in awide variety of infectious disease detection and monitoring assays.
Yu LiuChen LiZhi LiSamuel D.H. ChanDaisuke EtoWarren WuYanping ZhangRing‐Ling ChienHenry G. WadaMichael GreensteinShinji Satomura
Charles L. SolidayLisa KrivokopichVictoria Rothwell
Bo YangJiaxin HuangChunxian TaoZhenqing LiDawei ZhangYoshinori Yamaguchi
François BianchiHye Jin LeeHubert H. Girault
Sandeep Kumar JhaRohit ChandDawoon HanYou‐Cheol JangGyu-Sik RaJoung Sug KimBaek-Hie NahmYong‐Sang Kim