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The Lack of Binding Scale is a 5-item exploratory scale developed for the purposes of the study.
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As Chd1 binding scales with PolII density, only the genes in the highest quintile of PolII promoter occupancy were investigated to minimize the variation due to differences in PolII promoter occupancy.
Thus, the degree of DNA-bound p53 that is phosphorylated at S46 is higher upon Etoposide treatment and on a genome-wide DNA-binding scale a broad spectrum of individual target genes involved in different cellular functions can be found, including apoptotic target genes like BAX and PUMA.
The single property analysis revealed a strong and consistent RNA-binding property of the dataset: RNA-binding scales (Castello et al., 2012; Lewis et al., 2011; Terribilini et al., 2006) cover between 62 65%.
The binding energy scale was calibrated to 284.5 eV for the main C 1s peak.
The binding energy scale was calibrated with pure and clean Cu, Ag, and Au samples.
The binding energy scale was calibrated with the Cu 3p3/2 (933 eV) and Au 4f7/2 (84 eV) peaks.
The binding energy scale was calibrated using the Ge 3d5/2 peak at 29.4 eV.
The binding energy scale was charge referenced to the C1s photoelectron peak at 285 eV.
The binding energy scale was calibrated using the C1s spectral component at 284.8 eV.
The binding energy scale was calibrated by measuring the C 1 s peak at 285.0 eV.
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