Skip to main content
. Author manuscript; available in PMC: 2016 Aug 31.
Published in final edited form as: Dalton Trans. 2012 Mar 22;41(21):6558–6566. doi: 10.1039/c2dt12207c

Fig. 8.

Fig. 8

Detection of H2O2 from samples of Aβ, Cu2+, and/or a compound in the presence of ascorbate by a horseradish peroxidase (HRP)/Amplex Red assay. Lanes: (1) Aβ; (2) Aβ + Cu2+; (3) Aβ + Cu2+ + FL1; (4) Aβ + Cu2+ + FL2; (5) Aβ + Cu2+ + FL3; (6) Aβ + Cu2+ + FL4 ; (7) Aβ + Cu2+ + myricetin. Experimental conditions: [Aβ] = 200 nM, [Cu2+] = 400 nM, [ligand] = 800 nM, [ascorbate] = 10 μM, [Amplex Red] = 50 μM, [HRP] = 1 U/mL, λex/em = 530/590 nm. Catalase attenuates the fluorescence signal.