TY - JOUR
T1 - Automated microdroplet platform for sample manipulation and polymerase chain reaction
AU - Chabert, Max
AU - Dorfman, Kevin D.
AU - De Cremoux, Patricia
AU - Roeraade, Johan
AU - Viovy, Jean Louis
PY - 2006/11/15
Y1 - 2006/11/15
N2 - We present a fully automated system performing continuous sampling, reagent mixing, and polymerase chain reaction (PCR) in microdroplets transported in immiscible oil. Sample preparation and analysis are totally automated, using an original injection method from a modified 96-well plate layered with three superimposed liquid layers and in-capillary laser-induced fluorescence endpoint detection. The process is continuous, allowing sample droplets to be carried uninterruptedly into the reaction zone while new drops are aspirated from the sample plate. Reproducible amplification, negligible cross-contamination, and detection of low sample concentrations were demonstrated on numerous consecutive sample drops. The system, which opens the route to strong reagents and labor savings in high-throughput applications, was validated on the clinically relevant quantification of progesterone receptor gene expression in human breast cancer cell lines.
AB - We present a fully automated system performing continuous sampling, reagent mixing, and polymerase chain reaction (PCR) in microdroplets transported in immiscible oil. Sample preparation and analysis are totally automated, using an original injection method from a modified 96-well plate layered with three superimposed liquid layers and in-capillary laser-induced fluorescence endpoint detection. The process is continuous, allowing sample droplets to be carried uninterruptedly into the reaction zone while new drops are aspirated from the sample plate. Reproducible amplification, negligible cross-contamination, and detection of low sample concentrations were demonstrated on numerous consecutive sample drops. The system, which opens the route to strong reagents and labor savings in high-throughput applications, was validated on the clinically relevant quantification of progesterone receptor gene expression in human breast cancer cell lines.
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U2 - 10.1021/ac061205e
DO - 10.1021/ac061205e
M3 - Article
C2 - 17105164
AN - SCOPUS:33751212797
SN - 0003-2700
VL - 78
SP - 7722
EP - 7728
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 22
ER -