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Separate vials make sense when you need to increase one peptide disproportionately
copper complexation is typically performed by mixing the tripeptide with copper(II) salts (chloride, acetate, or sulfate) at controlled pH, with the resulting complex purified by chromatography
Institutions are supra-individual units of analysis, with properties that cannot be reduced to the aggregation of individual motives or interests (Powell, Di Maggio, 1991)
This drawback can be due to only one side of the NO-system employed in the studies (i.e., decreased function by L-NAME application) while the other part remained unchecked (i.e., over-increased function by L-arginine, and vice versa) [124,125]
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