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. 2020 Oct 22;28(6):649–666. doi: 10.1038/s41417-020-00246-9

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© The Author(s) 2020

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — Cellular extracts of Raji B cells treated for 5 min at 37 °C with or without EGF, NHL-a101 and NHL-a102 were evaluated for phosphorylation of EGFR family members by a human phosphorylation array. The intensities of the phospho-protein signals were quantified by densitometric analysis and normalized to either positive controls or not treated cells as suggested by the manufacturer’s instructions. Values reported for protein phosphorylation levels are representative of one representative experiment of 3 with similar results. NT, not treated.