Double-stranded DNA amplified by polymerase chain reaction (PCR) was detected by peptide nucleic acid (PNA) using a BIAcore(TM) 2000 biosensor based on surface plasmon resonance (SPR). PNA is an artificial oligo amide that is capable of forming highly stable complexes with complementary oligonucleotides. We succeeded in the direct detection of double-stranded DNA, amplified by PCR with high-sequence specificity. It was shown that the target DNA was available for detection over the range of 40-160 nM. Therefore, the detection limit was 7.5 pmol of the target DNA (143 bases, applied volume 30 mu l) Our DNA detection system, the combination of BIAcore(TM) and the probe PNA, could detect the target DNA with good reproducibility. In this report, we show that our system is a powerful tool for the diagnosis of pathologically significant DNA. (C) 1999 Elsevier Science S.A. All rights reserved.
机构:
Nucleic Acid Center, Department of Biochemistry and Molecular Biology, University of Southern Denmark, Campusvej 55, Odense M, 5230, DenmarkNucleic Acid Center, Department of Biochemistry and Molecular Biology, University of Southern Denmark, Campusvej 55, Odense M, 5230, Denmark
Veedu, Rakesh N.
Vester, Birte
论文数: 0引用数: 0
h-index: 0
机构:
Nucleic Acid Center, Department of Biochemistry and Molecular Biology, University of Southern Denmark, Campusvej 55, Odense M, 5230, DenmarkNucleic Acid Center, Department of Biochemistry and Molecular Biology, University of Southern Denmark, Campusvej 55, Odense M, 5230, Denmark
Vester, Birte
Wengel, Jesper
论文数: 0引用数: 0
h-index: 0
机构:
Nucleic Acid Center, Department of Biochemistry and Molecular Biology, University of Southern Denmark, Campusvej 55, Odense M, 5230, DenmarkNucleic Acid Center, Department of Biochemistry and Molecular Biology, University of Southern Denmark, Campusvej 55, Odense M, 5230, Denmark
Wengel, Jesper
Journal of the American Chemical Society,
2008,
130
(26):
: 8124
-
8125