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Samples were exposed to H 2 O 2 or buffer (blank control), and absorbance was recorded immediately at 240 nm in eight intervals ranging from 1 to 40 s
Cytokine levels were acquired using a FACSCanto II flow cytometer (BD Biosciences) and analyses were performed using LEGENDplex data analysis software (BioLegend)
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[27] Axelsson AS, Tubbs E, Mecham B, et al