Fluorescence detection of specific sequence of nucleic acids by oxazole yellow-linked oligonucleotides. Homogeneous quantitative monitoring of in vitro transcription
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作者:
Ishiguro, T
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KYOTO UNIV,CHEM RES INST,UJI,KYOTO 611,JAPANKYOTO UNIV,CHEM RES INST,UJI,KYOTO 611,JAPAN
Ishiguro, T
[1
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Saitoh, J
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KYOTO UNIV,CHEM RES INST,UJI,KYOTO 611,JAPANKYOTO UNIV,CHEM RES INST,UJI,KYOTO 611,JAPAN
Saitoh, J
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Yawata, H
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KYOTO UNIV,CHEM RES INST,UJI,KYOTO 611,JAPANKYOTO UNIV,CHEM RES INST,UJI,KYOTO 611,JAPAN
Yawata, H
[1
]
Otsuka, M
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KYOTO UNIV,CHEM RES INST,UJI,KYOTO 611,JAPANKYOTO UNIV,CHEM RES INST,UJI,KYOTO 611,JAPAN
Otsuka, M
[1
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Inoue, T
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KYOTO UNIV,CHEM RES INST,UJI,KYOTO 611,JAPANKYOTO UNIV,CHEM RES INST,UJI,KYOTO 611,JAPAN
Inoue, T
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Sugiura, Y
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KYOTO UNIV,CHEM RES INST,UJI,KYOTO 611,JAPANKYOTO UNIV,CHEM RES INST,UJI,KYOTO 611,JAPAN
We have developed a fluorescent DNA probe, oxazole yellow (YO)-linked oligonucleotide complementary to a target DNA/RNA, which can enhance the fluorescence on hybridizing with a target nucleotide. We demonstrated the applicability of the YO-linked oligonucleotide probe to real-time monitoring of the in vitro transcription process of a plasmid DNA constructed containing the 5'-terminus non-coded region of hepatitis C virus RNA. In the process of in vitro transcription in the presence of YO-linked complementary oligonucleotide, the fluorescence of the reaction mixture showed a time-dependent linear increase corresponding to the generated target RNA product.