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. 2021 Jun 28;413(20):4925–4937. doi: 10.1007/s00216-021-03458-6

Table 1.

Composition of the buffers used in this work

Name Composition
BufferDNAzyme 50 mM KCl and 20 mM MgCl2 in 10 mM Tris-HCl, pH 8.3
BufferA 5 mM KCl and 1 mM MgCl2 in 20 mM Tris-HCl, pH 8.3 (used in all the measurements, unless stated otherwise)
BufferB 5 mM KCl, 1 mM MgCl2, and 0.1 mM EDTA in 10 mM Tris-HCl, pH 8.0
BufferC 5 mM KCl and 1 mM MgCl2 in 10 mM Tris-HCl, pH 8.0