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Cloning of fluorescent reporter fusions The cloning of all fluorescent reporter fusion constructs was performed as described earlier (Meyer et al., m GFP) by one amino acid exchange (alanine 206 to lysine, Zacharias et al., via NotI and PstI/SdaI), resulting in vector p m GFP-NXn (pos

These systems often include multiple tools such as sterile empty vials , 10ml sterile vials , and supporting liquids for other compounds

There is a high degree of correlation between the ATAC-seq groups and RNA-seq clusters in both direction and timing of differential chromatin accessibility and gene expression ( Figure 2D ), showing that the BDG-induced changes in chromatin accessibility are associated with transcriptional changes of proximal genes