DC Field | Value | Language |
---|---|---|
dc.contributor.author | Hansol Kim | - |
dc.contributor.author | S Lee | - |
dc.contributor.author | Y Ju | - |
dc.contributor.author | H Kim | - |
dc.contributor.author | Hyowon Jang | - |
dc.contributor.author | Yeonkyung Park | - |
dc.contributor.author | S M Lee | - |
dc.contributor.author | D Yong | - |
dc.contributor.author | Taejoon Kang | - |
dc.contributor.author | H G Park | - |
dc.date.accessioned | 2024-03-11T16:32:47Z | - |
dc.date.available | 2024-03-11T16:32:47Z | - |
dc.date.issued | 2024 | - |
dc.identifier.issn | 0956-5663 | - |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/33790 | - |
dc.description.abstract | We herein present a multifunctional self-priming hairpin probe-based isothermal amplification, termed MSH, enabling one-pot detection of target nucleic acids. The sophisticatedly designed multifunctional self-priming hairpin (MSH) probe recognizes the target and rearranges to prime itself, triggering the amplification reaction powered by the continuously repeated extension, nicking, and target recycling. As a consequence, a large number of double-stranded DNA (dsDNA) amplicons are produced that could be monitored in real-time using a dsDNA-intercalating dye. Based on this unique design approach, the nucleocapsid (N) and the open reading frame 1 ab (ORF1ab) genes of SARS-CoV-2 were successfully detected down to 1.664 fM and 0.770 fM, respectively. The practical applicability of our method was validated by accurately diagnosing 60 clinical samples with 93.33% sensitivity and 96.67% specificity. This isothermal one-pot MSH technique holds great promise as a point-of-care testing protocol for the reliable detection of a wide spectrum of pathogens, particularly in resource-limited settings. | - |
dc.publisher | Elsevier | - |
dc.title | Multifunctional self-priming hairpin probe-based isothermal nucleic acid amplification and its applications for COVID-19 diagnosis | - |
dc.title.alternative | Multifunctional self-priming hairpin probe-based isothermal nucleic acid amplification and its applications for COVID-19 diagnosis | - |
dc.type | Article | - |
dc.citation.title | Biosensors & Bioelectronics | - |
dc.citation.number | 0 | - |
dc.citation.endPage | 116147 | - |
dc.citation.startPage | 116147 | - |
dc.citation.volume | 253 | - |
dc.contributor.affiliatedAuthor | Hansol Kim | - |
dc.contributor.affiliatedAuthor | Hyowon Jang | - |
dc.contributor.affiliatedAuthor | Yeonkyung Park | - |
dc.contributor.affiliatedAuthor | Taejoon Kang | - |
dc.contributor.alternativeName | 김한솔 | - |
dc.contributor.alternativeName | 이서영 | - |
dc.contributor.alternativeName | 주용 | - |
dc.contributor.alternativeName | 김효용 | - |
dc.contributor.alternativeName | 장효원 | - |
dc.contributor.alternativeName | 박연경 | - |
dc.contributor.alternativeName | 이상모 | - |
dc.contributor.alternativeName | 용동은 | - |
dc.contributor.alternativeName | 강태준 | - |
dc.contributor.alternativeName | 박현규 | - |
dc.identifier.bibliographicCitation | Biosensors & Bioelectronics, vol. 253, pp. 116147-116147 | - |
dc.identifier.doi | 10.1016/j.bios.2024.116147 | - |
dc.subject.keyword | Self-priming hairpin probe | - |
dc.subject.keyword | Isothermal amplification | - |
dc.subject.keyword | Molecular diagnostics | - |
dc.subject.keyword | SARS-CoV-2 | - |
dc.subject.keyword | COVID-19 | - |
dc.subject.local | Self-priming hairpin probe | - |
dc.subject.local | Isothermal amplification | - |
dc.subject.local | isothermal amplification | - |
dc.subject.local | Molecular diagnostic | - |
dc.subject.local | Molecular diagnostics | - |
dc.subject.local | molecular diagnostic | - |
dc.subject.local | Molecular Diagnostics | - |
dc.subject.local | SARS-CoV-2 | - |
dc.subject.local | SARS-Cov-2 | - |
dc.subject.local | COVID-19 | - |
dc.subject.local | Covid19 | - |
dc.subject.local | COVID19 | - |
dc.subject.local | CCOVID 19 | - |
dc.subject.local | COVID?19 | - |
dc.description.journalClass | Y | - |
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