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A 50-nm-thick compact TiO2 (c-TiO2c-TiO2 layer was synthesized by a procedure reported in our previous work [31].
This was prepared by a procedure reported by Eggert et al. [4], where hydrazine was added as a reduction agent to an appropriate amount of selenium powder dispersed in DMF, combined with 25% solution of tetraethylammonium hydroxide as an organic base.
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The N-TiO2 was prepared by the sol gel method [20, 21] and it was done by following a procedure reported by Wu et al. [22] where isopropyl alcohol (C3H7OH) and Ti OC4H9 4, in acidic medium, were used to prepare TiO2 nanoparticles.
We developed a procedure to exchange Cu+ ions with In3+ ions in Cu3- x P NCs, by adapting a procedure reported by Beberwyck et al. on Cd3P2 NCs.
The phosphoramidite of d-isoCMe 15 was accessed by following a procedure reported by Seela[ 23] (Scheme 3), starting from thymidine 14.
Highly enriched Ni was plated on a gold disk (24 mm in diameter and 2 mm thick) by electrodeposition using a procedure reported previously [ 14].
Bone calcium was determined by atomic absorption spectrophotometry (S series GE712405 v1.30; Thermo Fisher Scientific, Waltham, MA, USA) using a procedure reported by Harrison et al,15 with some modifications.
Abasic (AP) sites were measured based on a procedure reported by Nakamura and Swenberg [21].
CB[7] was synthesized according to a procedure reported by Day.
ASE was analyzed on an RP-18 column (250 mm × 4 mm, 5 μm particles) according to a procedure reported by Peng et al. [ 11].
Chemical competent cells of E. coli JM 109 (DE3) were prepared according to a procedure reported previously by Sambrook et al. (1989).
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