“…Moreover, EIS circumvents the labeling of at least one compound of the assay with, for example, enzymes, fluorophores, or redox reporters and can hence be considered as a label-free approach for detecting complementary recognition events at surfaces. [6][7][8][9] Therefore, EIS has been successfully applied for the detection of DNA conductivity, [10] DNA hybridization, [11][12][13][14][15] single-nucleotide mismatches in double-stranded DNA (dsDNA), [16] in situ hybridization of PNA/DNA, [17] DNA and RNA replication, [18,19] and the interaction of metal ions with DNA. [20,21] DNA detection by means of EIS is based on the repulsion between the DNA-modified electrode and a free-diffusing redox reporter, typically [Fe(CN) 6 ] 3À/4À .…”