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On-chip single-copy real-time reverse-transcription PCR in isolated picoliter droplets.
Beer, N Reginald; Wheeler, Elizabeth K; Lee-Houghton, Lorenna; Watkins, Nicholas; Nasarabadi, Shanavaz; Hebert, Nicole; Leung, Patrick; Arnold, Don W; Bailey, Christopher G; Colston, Bill W.
Affiliation
  • Beer NR; Lawrence Livermore National Laboratory, 7000 East Avenue, Livermore, California 94551, USA. beer2@llnl.gov
Anal Chem ; 80(6): 1854-8, 2008 Mar 15.
Article in En | MEDLINE | ID: mdl-18278951
The first lab-on-chip system for picoliter droplet generation and RNA isolation, followed by reverse transcription, and PCR amplification with real-time fluorescence detection in the trapped droplets has been developed. The system utilized a shearing T-junction in a fused-silica device to generate a stream of monodisperse picoliter-scale 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 thermal cycling for reverse transcription and subsequent PCR amplification without droplet motion. This combination of the established real-time reverse transcription-PCR assay with digital microfluidics is ideal for isolating single-copy RNA and virions from a complex environment and will be useful in viral discovery and gene-profiling applications.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Reverse Transcriptase Polymerase Chain Reaction Language: En Journal: Anal Chem Year: 2008 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Reverse Transcriptase Polymerase Chain Reaction Language: En Journal: Anal Chem Year: 2008 Document type: Article Affiliation country: United States Country of publication: United States