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All substrates were used directly after activation.
All substrates were tested at 2.5 mM.
All substrates were treated in methanol before the deposition process.
All substrates used in this work were commercial 2-in.
All substrates are covered by a native oxide layer.
All substrates used for enzymatic studies were procured from Merck.
All substrates were cleaned with acetone, ethanol, and deionized water in sequence before thin film deposition.
All substrates were dissolved in 250 mM potassium phosphate buffer (pH 6.5).
All substrates were cleaned using Shiraki method followed with HF treatment to form hydrogen terminated surface.
All substrates were used in 250 µM final concentration in all the assays.
All substrates were sequenced to verify insertion and orientation of the inserts.
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