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1. H1 from 0–12 h embryos was purified, digested with trypsin, and submited to β-elimination followed by 1,4-addition of 2-mercaptoethanol


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2. Histone H1 from 2–3 h, 3–6 h, 6–9 h, 9–12 h and 12–15 h was isolated and digested with trypsin


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3. H1 from 0–12 h embryos was purified and digested with Asp-N


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4. A) Separation of the peptides produced by AspN digestion of H1 from 0–12 h embryos over a C18 column


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5. H1 from 0–12 h embryos was isolated and digested with AspN (A), trypsin (B) or Glu-C (C, D)


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6. Probing the Conformation of the ISWI ATPase Domain With Genetically Encoded Photoreactive

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7. Fine mapping of posttranslational modifications of the linker histone H1 from Drosophila melanogaster

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8. Site-specific acetylation of ISWI by GCN5-0


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9. Site-specific acetylation of ISWI by GCN5-1


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10. Site-specific acetylation of ISWI by GCN5-2


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