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. 2019 Aug 14;14(8):e0217532. doi: 10.1371/journal.pone.0217532

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© 2019 Debrand et al

This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig 7 — Chromatin immunoprecipitation assays for histone H3 acetylation (H3ac), di-methylated lysine 4 of histone H3 (H3K4me2), and tri-methylated lysine 4 of histone H3 (H3K4me3); ●, wild-type adult erythroid cells from line 264W [10]; , adult erythroid cells from line Δ115. Coordinates in bp are shown along the x axis with HBE start site as +1. Bound versus input ratios were calculated and normalized to the most 3’ primer pair, located just downstream of 3’HS1 in the ORG cluster. A map of the locus is shown below the graphs.

Inline graphic — Chromatin immunoprecipitation assays for histone H3 acetylation (H3ac), di-methylated lysine 4 of histone H3 (H3K4me2), and tri-methylated lysine 4 of histone H3 (H3K4me3); ●, wild-type adult erythroid cells from line 264W [10]; , adult erythroid cells from line Δ115. Coordinates in bp are shown along the x axis with HBE start site as +1. Bound versus input ratios were calculated and normalized to the most 3’ primer pair, located just downstream of 3’HS1 in the ORG cluster. A map of the locus is shown below the graphs.