. 2017 Feb 8;7(18):10660–10667. doi: 10.1039/c6ra27684a

Table 3. Shift of melting temperature, ΔT _m, of quadruplex DNA F21T in the presence of the ligands 2 and 4b–d at different LDR without and with the duplex DNA ds26 as determined by fluorimetric thermal denaturation studies.

Ligand	ΔT _m/°C at different LDR ^a
	Without ds26		With ds26 ^b
	2.5	5.0	2.5	5.0
2BF₄	21.7	27.0	20.0	26.5
4b	28.2	31.6	21.3	30.7
4c	25.9	31.8	23.3	29.4
4d	28.1	32.9	25.5	31.4

^aΔT _m of F21T; c _F21T = 0.2 μM (in oligonucleotide); KCl–LiCl–Na–cacodylate buffer (10 mM K⁺, 10 mM Na⁺, 90 mM Li⁺, pH 7.2); λ _ex = 470 nm; λ _em = 515 nm; estimated error: ±0.5 °C of the given data.

^b c _ds26 = 3.0 μM.

Table 3. Shift of melting temperature, ΔT m, of quadruplex DNA F21T in the presence of the ligands 2 and 4b–d at different LDR without and with the duplex DNA ds26 as determined by fluorimetric thermal denaturation studies.

Table 3. Shift of melting temperature, ΔT _m, of quadruplex DNA F21T in the presence of the ligands 2 and 4b–d at different LDR without and with the duplex DNA ds26 as determined by fluorimetric thermal denaturation studies.