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4 protocols using co no3 2 6h2o

1

Photoelectrochemical Properties of InN Films

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InN/titanium paste electrodes were prepared to examine the photoelectrochemical properties of InN films with a thickness of 0.5 μm. To prepare InN electrodes, the as-synthesized InN powder was mixed with a 2-butanol solution (20 wt%, Wako, 99%) for 24 h. The paste was deposited on a Ti substrate (Nilaco) by the doctor blade technique using scotch tape as a spacer. Prior to deposition, the Ti substrate was cleaned with an etching solution (a mixture of 7 mL distilled water, 5 mL HNO3 (Nacalai Tesque, 60%), and 1 mL HF (Wako, 46%)). The heat treatment was performed at 350 °C for 2 h under a N2 atmosphere. Then, 5 mL of a NaOH (5 mM, Kanto, 97%) solution was added to 20 mL of a Co(NO3)2·6H2O (5 mM, Wako, 99.5%) solution, and a portion of this mixture was dropped onto the InN film. Subsequently, heat treatment was performed at 350 °C for 2 h under a N2 atmosphere.
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2

Preparative Procedures for Biomolecules and Metal Ions

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Deoxyribonucleic acid (DNA) from salmon milt (ca. 100–300 bp, purity >90%) was purchased from Fujifilm Wako (Osaka, Japan). RNA from yeast was purchased from Tokyo Chemical Industry Inc. (Tokyo, Japan). Cytidine-5′-monophosphate (purity 98%), adenosine-5′-monophasphate (purity 98%), guanosine-5′-monophasphate (purity 97%), and uridine-5′-monophasphate (purity 98%) were purchased from Combi Blocks Inc. (San Diego, CA, USA). KNO3, NaCl, CaCl2·2H2O, Al(NO3)3·9H2O, Zn(NO3)2·6H2O, Co(NO3)2·6H2O, Pb(NO3)2, NiCl2·6H2O, Cu(NO3)2·3H2O from Fujifilm Wako (Osaka, Japan), Hg(NO3)2·H2O and AgNO3 from Sigma-Aldrich (St. Louis, MO, USA), Cd(NO3)2·9H2O from Combi-Blocks (San Diego, CA, USA), and MgCl2·6H2O from Kishida Chemicals (Osaka, Japan) were used for metal ion sensing experiments, as received. Unless otherwise mentioned, deionized water of resistivity 18.2 MOhm⋅cm and purified using a Purelab Chorus 1 Life Science apparatus was used in all experiments.
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3

Synthesis of Transition Metal-Doped Carbon Materials

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La(NO3)3·6H2O, Ca(NO3)2·4H2O, Ba(CH3COO)2, Mn(NO3)2·6H2O, Ga(NO3)3·nH2O, Co(NO3)2·6H2O (Wako Pure Chemical Industries, Ltd), Ca(CH3COO)2·H2O, Sr(NO3)2, Sr(CH3COO)2·0.5H2O, Mn(CH3COO)2·4H2O, Fe(NO3)3·9H2O, Ni(NO3)2·6H2O, Al(NO3)3·9H2O, and ethanol (Kanto Chemical Co., Inc.) were used as received. Ketjen black (KB; Lion Specialty Chemicals Co., Ltd) and carbon nanofibers (CNFs; graphitized, iron-free; Sigma-Aldrich) were used as carbon sources for the PA method. The carbons were used as received when ethanol was used as the solvent. When water was used as the solvent, KB was calcined in air for 4 h at 773 K. The calcination process was aimed at enhancing the wettability of carbon to water by introducing oxygen-containing functional groups.
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4

Characterization of Recombinant PD-1 Protein

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Chemical reagents such as Tris, glycine, CuCl2·2H2O, FeCl3·6H2O, Co(NO3)2·6H2O, ZnSO4·7H2O, KCl, Na2HPO4·12H2O, NaCl, KH2PO4, EDTA·2Na and IPTG were purchased from Wako Pure Chemical Industries Ltd, Osaka, Japan (Guaranteed Reagent). CaCl2·2H2O was purchased from Nacalai Tesque (Kyoto, Japan). The synthetic substrate peptidyl-pNA, Arg-pNA, was purchased from Peptides Institute Inc., Osaka, Japan. Tryptone and yeast extract were purchased from Becton-Dickinson and Company, NJ, USA. A commercially available recombinant PD-1 molecule was used (ENZO Life Sciences Inc., product number ENZ-PRT190; PD-1 (aa 25–167) containing a 5′-His-tag, V5 epitope tag spacer, and FLAG-tag; a doublet at 40 kDa and 50 kDa: Farmingdale, NY). In our SDS-PAGE analysis, the doublet was observed at smaller positions (∼36 kDa and ∼42 kDa) than those stated in the description manual. This might be caused by the reducing conditions we employed.
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