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The experiments were done using 512-, 1,024-, and 2,048-dimensional 2,048-dimensional
The experiments were done using 2 h contact time and without any pH alteration (pH 4.4).
The experiments were done using specially designed flow cell equipped with Peltier element.
The experiments were done using the systems isopropanol-water-air and isopropanol-water-helium.
The experiments were done using different cell content SF6 gas at 800 mbar pressure as well as vacuum to investigate the surface morphology modification due to laser irradiation.
The experiments were done using fluorophore-loaded large unilamellar vesicles that had been doped with gA, and changes in the gA monomer↔dimer equilibrium were assayed using a gA channel-permeable fluorescence quencher (Tl+).
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In this section, all the experiments are done using the same methods, and the results are listed in Table 3.
In the revised manuscript, all statistical analyses have been performed using a FDR threshold of 0.05, when the experiment was done using 3 biological replicates (n=3).
Without any knowledge of the binding sites of the fragments, the docking experiments were done using a box containing the whole protein and positions were calculated for 50 conformers.
Because both non-overlapping dsRNA fragments resulted in similar phenotypes, the following experiments were done using the Tc-importin α1a fragment.
The cyanophage experiments were done using similar methods, except that the cyanophage (myovirus S-SSM1, on Synechococcus) was grown in Pro99 medium (Moore et al., 2007) and assayed for titre using the most probable number technique (Sullivan et al., 2003).
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