Handheld Real-Time PCR Device
| dc.contributor.author | Ahrberg, Christian D. | cs |
| dc.contributor.author | Ilic, Bojan Robert | cs |
| dc.contributor.author | Manz, Andreas | cs |
| dc.contributor.author | Neužil, Pavel | cs |
| dc.coverage.issue | 3 | cs |
| dc.coverage.volume | 16 | cs |
| dc.date.issued | 2016-01-04 | cs |
| dc.description.abstract | Here we report one of the smallest real-time polymerase chain reaction (PCR) system up to date with approximate size of 100 mm × 60 mm × 33 mm. The system is an autonomous unit requiring an external 12 V power supply. Four simultaneous reactions are performed in form of virtual reaction chambers (VRC) where a 200 nL sample is covered with mineral oil and placed on a glass cover slip. Fast, 40 cycle amplification of an amplicon from the H7N9 gene was used to demonstrate PCR performance. The standard curve slope was (-3.02 ± 0.16) cycles at threshold per decade (mean ± standard deviation) corresponding to an amplification efficiency of (0.91 ± 0.05) per cycle (mean ± standard deviation). The PCR device was capable of detecting a single deoxyribonucleic acid (DNA) copy. These results further suggest that our handheld PCR device may have broad, technologically-relevant applications extending to rapid detection of infectious diseases in small clinics. | en |
| dc.description.abstract | Here we report one of the smallest real-time polymerase chain reaction (PCR) system up to date with approximate size of 100 mm × 60 mm × 33 mm. The system is an autonomous unit requiring an external 12 V power supply. Four simultaneous reactions are performed in form of virtual reaction chambers (VRC) where a 200 nL sample is covered with mineral oil and placed on a glass cover slip. Fast, 40 cycle amplification of an amplicon from the H7N9 gene was used to demonstrate PCR performance. The standard curve slope was (-3.02 ± 0.16) cycles at threshold per decade (mean ± standard deviation) corresponding to an amplification efficiency of (0.91 ± 0.05) per cycle (mean ± standard deviation). The PCR device was capable of detecting a single deoxyribonucleic acid (DNA) copy. These results further suggest that our handheld PCR device may have broad, technologically-relevant applications extending to rapid detection of infectious diseases in small clinics. | en |
| dc.format | text | cs |
| dc.format.extent | 586-592 | cs |
| dc.format.mimetype | application/pdf | cs |
| dc.identifier.citation | Lab on a chip. 2016, vol. 16, issue 3, p. 586-592. | en |
| dc.identifier.doi | 10.1039/c5lc01415h | cs |
| dc.identifier.issn | 1473-0197 | cs |
| dc.identifier.other | 120126 | cs |
| dc.identifier.uri | http://hdl.handle.net/11012/61768 | |
| dc.language.iso | en | cs |
| dc.publisher | Royal Society of Chemistry | cs |
| dc.relation.ispartof | Lab on a chip | cs |
| dc.relation.uri | http://pubs.rsc.org/is/content/articlelanding/2015/lc/c5lc01415h#!divAbstract | cs |
| dc.rights | Creative Commons Attribution 3.0 Unported | cs |
| dc.rights.access | openAccess | cs |
| dc.rights.sherpa | http://www.sherpa.ac.uk/romeo/issn/1473-0197/ | cs |
| dc.rights.uri | http://creativecommons.org/licenses/by/3.0/ | cs |
| dc.subject | real-time PCR | en |
| dc.subject | palm-size | en |
| dc.subject | portable | en |
| dc.subject | standard curve | en |
| dc.subject | reproducibility | en |
| dc.subject | real-time PCR | |
| dc.subject | palm-size | |
| dc.subject | portable | |
| dc.subject | standard curve | |
| dc.subject | reproducibility | |
| dc.title | Handheld Real-Time PCR Device | en |
| dc.title.alternative | Handheld Real-Time PCR Device | en |
| dc.type.driver | article | en |
| dc.type.status | Peer-reviewed | en |
| dc.type.version | publishedVersion | en |
| sync.item.dbid | VAV-120126 | en |
| sync.item.dbtype | VAV | en |
| sync.item.insts | 2025.10.14 15:17:02 | en |
| sync.item.modts | 2025.10.14 09:57:07 | en |
| thesis.grantor | Vysoké učení technické v Brně. Středoevropský technologický institut VUT. Chytré nanonástroje | cs |
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