Nucleic acid microarrays created in the double-spiral format on a circular microfluidic disk
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review
Author(s)
Detail(s)
Original language | English |
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Pages (from-to) | 826-829 |
Journal / Publication | Lab on a Chip |
Volume | 8 |
Issue number | 5 |
Publication status | Published - 2008 |
Externally published | Yes |
Link(s)
Abstract
A microfluidic microarray that is created in the double spiral format has produced a greater density of probes than in our previous report. Using this double-spiral format together with centrifugal pumping for liquid delivery, 384 × 384 hybridization assays have been performed on one circular disk at one time, at the intersections between the spiral channels and spiral probe lines. Each sample was introduced into each inlet reservoir leading to 4 spiral channels and was analyzed independently, and so the hybridization results were self-corrected among the 4 spiral channels. In this work, fast microarray hybridizations have been successfully achieved by using both complementary oligonucleotides as well as PCR products prepared from plant fungal pathogen cultures. © The Royal Society of Chemistry.
Research Area(s)
Bibliographic Note
Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].
Citation Format(s)
Nucleic acid microarrays created in the double-spiral format on a circular microfluidic disk. / Chen, Hong; Wang, Lin; Li, Paul C. H.
In: Lab on a Chip, Vol. 8, No. 5, 2008, p. 826-829.
In: Lab on a Chip, Vol. 8, No. 5, 2008, p. 826-829.
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review