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. 2020 Apr 1;338:135864. doi: 10.1016/j.electacta.2020.135864

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© 2020 The Authors

This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

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Fig. 2 — ΔC_T values of 4 different bacterial cells lysed by ECL as a function of times () and of those extracted by a commercial DNA extraction kit () as a comparison; and the average pH values measured in the cathodic effluents (). For the ECL treated samples, ΔC_T values were calculated by subtracting C_T values of the suspended DNA in ECL treated samples from those in the untreated samples. For the samples extracted by the commercial kit, ΔC_T values were calculated by subtracting C_T values of the total DNA extracted by the commercial kit from those of the suspended DNA in the untreated samples.

Inline graphic — ΔC_T values of 4 different bacterial cells lysed by ECL as a function of times () and of those extracted by a commercial DNA extraction kit () as a comparison; and the average pH values measured in the cathodic effluents (). For the ECL treated samples, ΔC_T values were calculated by subtracting C_T values of the suspended DNA in ECL treated samples from those in the untreated samples. For the samples extracted by the commercial kit, ΔC_T values were calculated by subtracting C_T values of the total DNA extracted by the commercial kit from those of the suspended DNA in the untreated samples.