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In another study, Bae et al designed, synthesized and evaluated a series of ( E )- N -substituted benzylidene-hydroxy or methoxy-aniline derivatives (aza-resveratrol type) for their inhibitory effect on tyrosinase activity (Figure 6, 11a – 11e ) 67
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All samples from a 96-well plate were pooled and quantified by fragment size using the BioAnalyzer (Agilent Technologies) and concentration determined by Qubit (Invitrogen)
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