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Metal-Ion Amplified Sensor

For practical application, an ideal biosensor must be as straightforward as possible with least number of synthesis and analytical steps. Kraatz and coworkers introduced a simple, label-free and sensitive electrochemical sensor for single nucleotide mismatch detection. This approach relies on the diffusive property of the negatively charged redox probe [Fe(CN)6] and its interplay with matched and mismatched DNA films. [Pg.233]

Based on the initial SECM results, it was postulated that it should be possible to evaluate differences in R t directly by SECM and monitor the amperometric feedback current in the presence and absence of Zn +. The presence of SNP caused an increase in electron transfer rate constant, presumably due to better penetration of [Pg.234]

Recently, the effects of various metal ions on the electrochemical impedance spectra of 25-mer dsDNA films were reported. These metal ions include Mg + and Ca +, known to have high affinity for the phosphate backbone of DNA, the trivalent Al + and La +, and divalent transition metal ions Ni +, Cu +, Zn +, Cd + and Hg +. In all cases, the presence of metal ions decreases the of ds-DNA Films, presumably due to their coordination with the backbone phosphate and potentially association with one or more of the exocyclic [Pg.235]

Af-atoms ofthe purine bases. The ARct ofthe different metal ions was found in the order of Ca = Hg + Cd Ni  [Pg.236]

Cu + Zn + which is inversely proportional to their free energies of hydration (see Fig. 7.16) [99]. [Pg.236]


See other pages where Metal-Ion Amplified Sensor is mentioned: [Pg.206]    [Pg.228]    [Pg.233]   


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