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Volumn 17, Issue 6, 2003, Pages 307-311

Evaluation of the performance of LNA and MGB probes in 5′-nuclease PCR assays

Author keywords

5 Nuclease PCR; Locked Nucleic Acids; Minor Groove Binder; TaqMan probes

Indexed keywords

ACCURACY; ARTICLE; BACTERIUM IDENTIFICATION; COMPARATIVE STUDY; CONTROLLED STUDY; EVALUATION; LOCKED NUCLEIC ACID PROBE; MINOR GROOVE BINDER PROBE; MOLECULAR PROBE; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; STAPHYLOCOCCUS AUREUS;

EID: 0242320540     PISSN: 08908508     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mcp.2003.08.004     Document Type: Article
Times cited : (62)

References (10)
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  • 2
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  • 3
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    • Standardization and quality control of PCR analyses
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  • 5
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    • Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridisation
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  • 6
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    • Efficient priming of PCR with short oligonucleotides conjugated to a minor groove binder
    • Afonina I., Zivarts M., Kutyavin I., Lukhtanov E., Gamper H., Meyer R.B. Efficient priming of PCR with short oligonucleotides conjugated to a minor groove binder. Nucl Acids Res. 25:1997;2657-2660.
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  • 8
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    • Locked nucleic acid (LNA): Fine-tuning the recognition of DNA and RNA
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  • 9
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    • Design considerations and effects of LNA in PCR primers
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  • 10
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    • Detection and genotyping by real-time PCR of the staphylococcal enterotoxin genes sea to sej
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.