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Etylation competent HAT complexes. In contrast, chromosomes of dAda2bSEGFP transgene-carriers revealed significantly weaker dSAGA-specific acetylation signals (Figure 4A). The transgene directing the expression of untagged dADA2bS, which was more potent in rescue experiments, was also more effective in restoring H3 acetylation. Immunodetection of H3K9ac in extracts of dAda2b mutants and transgenec
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Etylation competent HAT complexes. In contrast, chromosomes of dAda2bSEGFP transgene-carriers revealed significantly weaker dSAGA-specific acetylation signals (Figure 4A). The transgene directing the expression of untagged dADA2bS, which was more potent in rescue experiments, was also more effective in restoring H3 acetylation. Immunodetection of H3K9ac in extracts of dAda2b mutants and transgenec
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Xtraction protocol is at least comparable with other cell wall proteome studies in terms of protein recovery rate. Furthermore, the mucilage proteins identified include all proteins believed to be secreted to the mucilage pocket that are not membrane anchored: MUM2, SBT1.7, BXL1, and PER36 (Dean et al., 2007; Macquet et al., 2007b; Rautengarten et al., 2008; Arsovski et al., 2009; Kunieda et al.,
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