DC Field | Value | Language |
---|---|---|
dc.contributor.author | Jung, Cheul-Hee | ko |
dc.contributor.author | Chung, Ji-Won | ko |
dc.contributor.author | Kim, Un-Ok | ko |
dc.contributor.author | Kim, Min-Hwan | ko |
dc.contributor.author | Park, Hyun-Gyu | ko |
dc.date.accessioned | 2010-12-22T08:39:59Z | - |
dc.date.available | 2010-12-22T08:39:59Z | - |
dc.date.created | 2012-02-06 | - |
dc.date.created | 2012-02-06 | - |
dc.date.issued | 2010-07 | - |
dc.identifier.citation | ANALYTICAL CHEMISTRY, v.82, no.14, pp.5937 - 5943 | - |
dc.identifier.issn | 0003-2700 | - |
dc.identifier.uri | http://hdl.handle.net/10203/21190 | - |
dc.description.abstract | An iTPA (isothermal target and signaling probe amplification) method for the quantitative detection of nucleic acids, based on a combination of novel ICA (isothermal chain amplification) and fluorescence resonance energy transfer cycling probe technology (FRET CPT), is described. In the new ICA method, which relies on the strand displacement activity of DNA polymerase and the RNA degrading activity of RNase H, two displacement events occur in the presence of four specially designed primers. This phenomenon leads to powerful amplification of target DNA. Since the amplification is initiated only after hybridization of the four primers, the ICA method leads to high specificity for the target sequence. As part of the new ICA method, iTPA is achieved by incorporating FRET CPT to generate multiple fluorescence signals from a single target molecule. Using the resulting dual target and signaling probe amplification system, even a single copy level of a target gene can be successfully detected and quantified under isothermal conditions. | - |
dc.description.sponsorship | This work was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science, and Technology [No. 2009- 0080602], the Brain Korea 21 (BK21) program, and the Center for Ultramicrochemical Process Systems sponsored by KOSEF. | en |
dc.language | English | - |
dc.language.iso | en_US | en |
dc.publisher | AMER CHEMICAL SOC | - |
dc.subject | REAL-TIME PCR | - |
dc.subject | MOLECULAR DIAGNOSTICS | - |
dc.subject | DNA AMPLIFICATION | - |
dc.subject | ENZYMATIC AMPLIFICATION | - |
dc.subject | POLYMERASE | - |
dc.subject | SYSTEM | - |
dc.subject | MICROBIOLOGY | - |
dc.subject | MICROARRAY | - |
dc.subject | ASSAYS | - |
dc.title | Isothermal Target and Signaling Probe Amplification Method, Based on a Combination of an Isothermal Chain Amplification Technique and a Fluorescence Resonance Energy Transfer Cycling Probe Technology | - |
dc.type | Article | - |
dc.identifier.wosid | 000279727800005 | - |
dc.identifier.scopusid | 2-s2.0-77954626213 | - |
dc.type.rims | ART | - |
dc.citation.volume | 82 | - |
dc.citation.issue | 14 | - |
dc.citation.beginningpage | 5937 | - |
dc.citation.endingpage | 5943 | - |
dc.citation.publicationname | ANALYTICAL CHEMISTRY | - |
dc.identifier.doi | 10.1021/ac100606m | - |
dc.embargo.liftdate | 9999-12-31 | - |
dc.embargo.terms | 9999-12-31 | - |
dc.contributor.localauthor | Park, Hyun-Gyu | - |
dc.contributor.nonIdAuthor | Chung, Ji-Won | - |
dc.contributor.nonIdAuthor | Kim, Un-Ok | - |
dc.contributor.nonIdAuthor | Kim, Min-Hwan | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordPlus | REAL-TIME PCR | - |
dc.subject.keywordPlus | MOLECULAR DIAGNOSTICS | - |
dc.subject.keywordPlus | DNA AMPLIFICATION | - |
dc.subject.keywordPlus | ENZYMATIC AMPLIFICATION | - |
dc.subject.keywordPlus | POLYMERASE | - |
dc.subject.keywordPlus | SYSTEM | - |
dc.subject.keywordPlus | MICROBIOLOGY | - |
dc.subject.keywordPlus | MICROARRAY | - |
dc.subject.keywordPlus | ASSAYS | - |
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