| Literature DB >> 17929880 |
N Reginald Beer1, Benjamin J Hindson, Elizabeth K Wheeler, Sara B Hall, Klint A Rose, Ian M Kennedy, Bill W Colston.
Abstract
The first lab-on-chip system for picoliter droplet generation and PCR amplification with real-time fluorescence detection has performed PCR in isolated droplets at volumes 106 smaller than commercial real-time PCR instruments. The system utilized a shearing T-junction in a silicon device to generate a stream of monodisperse picoliter droplets that were isolated from the microfluidic channel walls and each other by the oil-phase carrier. An off-chip valving system stopped the droplets on-chip, allowing them to be thermally cycled through the PCR protocol without droplet motion. With this system, a 10-pL droplet, encapsulating less than one copy of viral genomic DNA through Poisson statistics, showed real-time PCR amplification curves with a cycle threshold of approximately 18, 20 cycles earlier than commercial instruments. This combination of the established real-time PCR assay with digital microfluidics is ideal for isolating single-copy nucleic acids in a complex environment.Entities:
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Year: 2007 PMID: 17929880 DOI: 10.1021/ac701809w
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986