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. Author manuscript; available in PMC: 2014 Jun 7.
Published in final edited form as: Lab Chip. 2013 Dec 7;13(23):4554–4562. doi: 10.1039/c3lc50698c

Fig. 1.

Fig. 1

Reconstructed ECL array data obtained from analytical spots containing optimized RuIIPVP/enzyme/DNA film assemblies reacted with oxygenated 25 µM of B[a]P + 1% DMSO in pH = 7.4 phosphate buffer with bioelectronic activation of cyt P450s at −0.65 V vs. Ag/AgCl (0.14 M KCl) for reaction times from 0–90 s. Control spots contained cyt P450 1B1 with or without EH, and were subjected to the same reaction conditions as above without bioelectronic activation of cyt P450s.