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공공누리This item is licensed Korea Open Government License

dc.contributor.author
박정훈
dc.contributor.author
박현규
dc.contributor.author
신인경
dc.contributor.author
장효원
dc.contributor.author
정예림
dc.contributor.author
정윤경
dc.contributor.author
조대연
dc.date.accessioned
2019-08-28T07:42:12Z
dc.date.available
2019-08-28T07:42:12Z
dc.date.issued
2017-05-15
dc.identifier.issn
0956-5663
dc.identifier.uri
https://repository.kisti.re.kr/handle/10580/14716
dc.description.abstract
We herein describe a new mass spectrometry-based method for multiplex SNP genotyping by utilizing allelespecific ligation and strand displacement amplification (SDA) reaction. In this method, allele-specific ligation is first performed to discriminate base sequence variations at the SNP site within the PCR-amplified target DNA. The primary ligation probe is extended by a universal primer annealing site while the secondary 
dc.language
eng
dc.relation.ispartofseries
Biosensors and Bioelectronics
dc.title
A mass spectrometry-based multiplex SNP genotyping by utilizing allelespecific ligation and strand displacement amplification
dc.citation.endPage
127
dc.citation.startPage
122
dc.citation.volume
91
dc.subject.keyword
SNP genotyping
dc.subject.keyword
BRCA gene
dc.subject.keyword
Allele-specific ligation
dc.subject.keyword
Strand displacement amplification
dc.subject.keyword
Label-free biosensor
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7. KISTI 연구성과 > 학술지 발표논문
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