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Lab Chip ; 8(12): 2071-8, 2008 Dec.
Article in English | MEDLINE | ID: mdl-19023470

ABSTRACT

We demonstrate the first integrated microfluidic tmRNA purification and nucleic acid sequence-based amplification (NASBA) device incorporating real-time detection. The real-time amplification and detection step produces pathogen-specific response in < 3 min from the chip-purified RNA from 100 lysed bacteria. On-chip RNA purification uses a new silica bead immobilization method. On-chip amplification uses custom-designed high-selectivity primers and real-time detection uses molecular beacon fluorescent probe technology; both are integrated on-chip with NASBA. Present in all bacteria, tmRNA (10Sa RNA) includes organism-specific identification sequences, exhibits unusually high stability relative to mRNA, and has high copy number per organism; the latter two factors improve the limit of detection, accelerate time-to-positive response, and suit this approach ideally to the detection of small numbers of bacteria. Device efficacy was demonstrated by integrated on-chip purification, amplification, and real-time detection of 100 E. coli bacteria in 100 microL of crude lysate in under 30 min for the entire process.


Subject(s)
Diagnostic Techniques and Procedures , Microfluidics , RNA, Bacterial/chemistry , Self-Sustained Sequence Replication , Escherichia coli/chemistry , Microfluidics/instrumentation , Microfluidics/methods , Self-Sustained Sequence Replication/instrumentation , Self-Sustained Sequence Replication/methods
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