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Subsequently, 0.4 mL of a PI staining/lysis solution (0.5% NP-40, 0.5 mM ethylenediaminetetraacetic acid [EDTA]) and 50 ΞΌL of RNase A (10 mg/mL in TrisβEDTA buffer, pH 8.0) solution were added
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doi: 10.1039/C7FO01185G
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