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. 2022 Feb 23;12(11):6416–6431. doi: 10.1039/d2ra00155a

Fig. 4. The gel shift assay of oligonucleotides' complexes of various lengths without linkers. (a) Lanes: 1, M20/N20 (1 : 1); 2, M20/N20/S10 (1 : 1 : 1); 3, M20/N20/S10 (1 : 1 : 10); 4, M20/N20l (1 : 1); 5, M20/N20l/S10 (1 : 1 : 1); 6, M20/N20l/S10 (1 : 1 : 10); 7, M20/N20l/S10l (1 : 1 : 1); 8, M20/N20l/S10l (1 : 1 : 10). (b) Lanes: 1, M30/N30 (1 : 1); 2, M30/N30/S15 (1 : 1 : 1); 3, M30/N30/S15 (1 : 1 : 10); 4, M30l/N30 (1 : 1); 5, M30l/N30/S15 (1 : 1 : 1); 6, M30l/N30/S15 (1 : 1 : 10); 7, M30l/N30/S15l (1 : 1 : 1); 8, M30l/N30/S15l (1 : 1 : 10). (c) Lanes: 1, M40/SX15 (2 : 1); 2, M40/SX15 (1 : 1); 3, M40/SX15/S25 (1 : 1 : 1); 4, M40/N40/SX15 (1 : 1 : 10); 5, M40/N40/SX15 (1 : 1 : 5); 6, M40/N40/SX15 (1 : 1 : 1); 7, M40/N40/SX15 (1 : 1 : 0.5); 8, M40/N40/SX15 (1 : 1 : 0.1); 9, M40/N40 (experiment at 15 °C). (d) Different types of complexes in the lanes are shown below the electropherogram. Full-size scans of gels are presented in Fig. S2.†.

Fig. 4