“…The supernatant was filtered with a 0.22 μm filter and diluted 10 times with 1× PBS at pH = 7.4. Later, different concentrations of histamine (0.04, 0.4, 2, 4, 10, 20, 30, 40, 100, 300, and 4000 mg/kg) and/or parvalbumin (4,10,20,30,40,100,200,300,400,2000, and 4000 mg/kg) were spiked in the sample. Then, in a 96-well assay plate were mixed 20 μL of the sample, 4 μL of each SERS tag, and 80 μL of running buffer (1% casein (w/w), 3% Tween 20 (w/w) in phosphate buffer 10 mM and pH 7.4), and a strip is introduced in the mixture.…”