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. 2022 Apr 8;14(8):1880. doi: 10.3390/cancers14081880

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© 2022 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

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Flow cytometry of BxPC3 and NHDF cells treated with dye-peptide A. The histograms of (a) Cy5/sulfoCy5-peptide A and (b) Cy3/sulfoCy3-peptide A. The analysis of (c) Cy5/sulfoCy5-peptide A and (d) Cy3/sulfoCy3-peptide A. Cells were incubated with 0.1 μM dye-peptide A at 37 °C for 3 or 24 h before flow cytometry. The data represent the mean ± SEM (n = 3). The statistical significance was assessed by Tukey-Kramer test (* p < 0.01).

Flow cytometry of BxPC3 and NHDF cells treated with dye-peptide A. The histograms of (a) Cy5/sulfoCy5-peptide A and (b) Cy3/sulfoCy3-peptide A. The analysis of (c) Cy5/sulfoCy5-peptide A and (d) Cy3/sulfoCy3-peptide A. Cells were incubated with 0.1 μM dye-peptide A at 37 °C for 3 or 24 h before flow cytometry. The data represent the mean ± SEM (n = 3). The statistical significance was assessed by Tukey-Kramer test (* p < 0.01).