DC Field | Value | Language |
---|---|---|
dc.contributor.author | Giyoung Shin | - |
dc.contributor.author | Dong-Kyun Kim | - |
dc.contributor.author | Doh, J | - |
dc.contributor.author | Daeyeon Lee | - |
dc.contributor.author | Nam Ki Lee | - |
dc.contributor.author | Jung, GY | - |
dc.date.accessioned | 2017-07-19T12:28:54Z | - |
dc.date.available | 2017-07-19T12:28:54Z | - |
dc.date.created | 2016-03-23 | - |
dc.date.issued | 2016-02 | - |
dc.identifier.issn | 0173-0835 | - |
dc.identifier.uri | https://oasis.postech.ac.kr/handle/2014.oak/35889 | - |
dc.description.abstract | Although the resolution of CE-SSCP has been significantly improved by using a poly(ethyleneoxide)-poly(propyleneoxide)-poly(ethyleneoxide) (PEO-PPO-PEO; Pluronic (R)) triblock copolymer as a separationmedium, CE-SSCP on a microchip format is not widely applicable because their resolution is limited by short channel length. Therefore, a strategy to improve the resolution in channels of limited lengths is highly required for enabling microchip-based CE-SSCP. In this study, we developed a high-resolution CE-SSCP microchip system by controlling the width of the pluronic-filled channel. We tested four different channel widths of 180, 240, 300, and 400 mu m, and found that 300 mu m showed the highest resolution in the separation of two pathogen specific markers. Potential applications of our method in various genetic analyses were also shown by using SNP markers for spinal muscular atrophy. | - |
dc.language | English | - |
dc.publisher | WILEY | - |
dc.relation.isPartOf | ELECTROPHORESIS | - |
dc.title | High-resolution pluronic-filled microchip CE-SSCP analysis system via channel width control | - |
dc.type | Article | - |
dc.identifier.doi | 10.1002/ELPS.201500427 | - |
dc.type.rims | ART | - |
dc.identifier.bibliographicCitation | ELECTROPHORESIS, v.37, no.4, pp.676 - 679 | - |
dc.identifier.wosid | 000370657900015 | - |
dc.date.tcdate | 2019-02-01 | - |
dc.citation.endPage | 679 | - |
dc.citation.number | 4 | - |
dc.citation.startPage | 676 | - |
dc.citation.title | ELECTROPHORESIS | - |
dc.citation.volume | 37 | - |
dc.contributor.affiliatedAuthor | Doh, J | - |
dc.contributor.affiliatedAuthor | Jung, GY | - |
dc.identifier.scopusid | 2-s2.0-84958593544 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.wostc | 1 | - |
dc.description.scptc | 1 | * |
dc.date.scptcdate | 2018-05-121 | * |
dc.type.docType | Article | - |
dc.subject.keywordPlus | DEPENDENT PROBE AMPLIFICATION | - |
dc.subject.keywordPlus | SPINAL MUSCULAR-ATROPHY | - |
dc.subject.keywordPlus | SENSITIVE CAPILLARY-ELECTROPHORESIS | - |
dc.subject.keywordPlus | CONFORMATION POLYMORPHISM ANALYSIS | - |
dc.subject.keywordPlus | TRIBLOCK COPOLYMER MATRIX | - |
dc.subject.keywordPlus | PATHOGEN DETECTION | - |
dc.subject.keywordPlus | SINGLE NUCLEOTIDE | - |
dc.subject.keywordPlus | ROBUST | - |
dc.subject.keywordPlus | GENE | - |
dc.subject.keywordAuthor | CE-SSCP | - |
dc.subject.keywordAuthor | Microchip | - |
dc.subject.keywordAuthor | Pathogen | - |
dc.subject.keywordAuthor | PEO-PPO-PEO triblock copolymer | - |
dc.subject.keywordAuthor | SNP | - |
dc.relation.journalWebOfScienceCategory | Biochemical Research Methods | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Analytical | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Chemistry | - |
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