Literature DB >> 16536436

Fully integrated miniature device for automated gene expression DNA microarray processing.

Robin Hui Liu1, Tai Nguyen, Kevin Schwarzkopf, H Sho Fuji, Alla Petrova, Tony Siuda, Kia Peyvan, Michael Bizak, David Danley, Andy McShea.   

Abstract

A DNA microarray with 12,000 features was integrated with a microfluidic cartridge to automate the fluidic handling steps required to carry out a gene expression study of the human leukemia cell line (K562). The fully integrated microfluidic device consists of microfluidic pumps/mixers, fluid channels, reagent chambers, and a DNA microarray silicon chip. Microarray hybridization and subsequent fluidic handling and reactions (including a number of washing and labeling steps) were performed in this fully automated and miniature device before fluorescent image scanning of the microarray chip. Electrochemical micropumps were integrated into the cartridge to provide pumping of liquid solutions. The device was completely self-contained: no external pressure sources, fluid storage, mechanical pumps, mixers, or valves were necessary for fluid manipulation, thus eliminating possible sample contamination and simplifying device operation. Fluidic experiments were performed to study the on-chip washing efficiency and uniformity. A single-color transcriptional analysis of K562 cells with a series of calibration controls (spiked-in controls) to characterize this new platform with regard to sensitivity, specificity, and dynamic range was performed. The device detected sample RNAs with a concentration as low as 0.375 pM. Experiment also showed that the performance of the integrated microfluidic device is comparable with the conventional hybridization chambers with manual operations, indicating that the on-chip fluidic handling (washing and reaction) is highly efficient and can be automated with no loss of performance. The device provides a cost-effective solution to eliminate labor-intensive and time-consuming fluidic handling steps in genomic analysis.

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Year:  2006        PMID: 16536436     DOI: 10.1021/ac0518553

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  3 in total

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Authors:  P Ajmone Marsan; S Tramontana; R Mazza
Journal:  Vet Res Commun       Date:  2007-08       Impact factor: 2.459

2.  Competitive reporter monitored amplification (CMA)--quantification of molecular targets by real time monitoring of competitive reporter hybridization.

Authors:  Thomas Ullrich; Eugen Ermantraut; Torsten Schulz; Katrin Steinmetzer
Journal:  PLoS One       Date:  2012-04-23       Impact factor: 3.240

3.  Simple system for isothermal DNA amplification coupled to lateral flow detection.

Authors:  Kristina Roskos; Anna I Hickerson; Hsiang-Wei Lu; Tanya M Ferguson; Deepali N Shinde; Yvonne Klaue; Angelika Niemz
Journal:  PLoS One       Date:  2013-07-26       Impact factor: 3.240

  3 in total

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