2010
DOI: 10.1016/j.ab.2009.11.019
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Electrochemical detection of short sequences of hepatitis C 3a virus using a peptide nucleic acid-assembled gold electrode

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Cited by 59 publications
(32 citation statements)
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“…Notably, higher temperatures, solutions with low ionic strength and shorter sequences can be employed. 29,30 Electrochemical DNA detection is facilitated by redox-active probes, which are introduced into the PNA recognition layer as free-diffusing redox mediator, 31 redox-active intercalators or minor-groove binders 28,[32][33][34][35] or as covalently bound redox labels. [36][37][38][39] Label-free PNA-based biosensors were, in general, exploited using electrochemical impedance spectroscopy, 31,40,41 Scanning…”
Section: Metal-containing Pnas For Biosensing Purposesmentioning
confidence: 99%
“…Notably, higher temperatures, solutions with low ionic strength and shorter sequences can be employed. 29,30 Electrochemical DNA detection is facilitated by redox-active probes, which are introduced into the PNA recognition layer as free-diffusing redox mediator, 31 redox-active intercalators or minor-groove binders 28,[32][33][34][35] or as covalently bound redox labels. [36][37][38][39] Label-free PNA-based biosensors were, in general, exploited using electrochemical impedance spectroscopy, 31,40,41 Scanning…”
Section: Metal-containing Pnas For Biosensing Purposesmentioning
confidence: 99%
“…A PNA probe was designed to recognize the target DNA related to tumour necrosis factor. Hejazi et al (2010) [216] developed an electrochemical DNA biosensor, using a gold electrode modified with a self-assembled monolayer composed of a PNA probe and 6-mercapto-1-hexanol. They covalently attached first the 14-mer PNA probe related to the hepatitis C virus genotype 3a (pHCV3a) core/E1 region on the electrode.…”
Section: Peptide Nucleic Acids (Pnas) Biosensorsmentioning
confidence: 99%
“…We did not find any report concerning the development of electrochemical biosensor for direct detection and discrimination of DNA sequence and single base mismatch in either double-stranded oligonucleotide (ds-oligonucleotide) chains or double-strand PCR products without denaturating dsDNA into ssDNA. We have previously reported the electrochemical detection of single-stranded DNA (ssDNA), using methylene blue (MB) [19][20][21] and brilliant cresyl blue (BCB) [22] reduction signals and also utilizing guanine oxidation signal [23][24][25]. Recently we have reported the development of a electrochemical biosensor for direct detection of double-stranded oligonucleotide corresponding to hepatitis C virus genotype 3a [26].…”
Section: Introductionmentioning
confidence: 99%