Figure 1From: Heterogeneity in the kinetics of nuclear proteins and trajectories of substructures associated with heterochromatinCellular patterns of selected proteins. The dynamics of selected proteins were studied using GFP technology combined with fluorescence recovery after photobleaching (FRAP). The following proteins were analysed: heterochromatin protein 1 (HP1α) (a1), (HP1β) (a2), B lymphoma Mo-MLV insertion region 1 (BMI1) (b), telomeric-repeat binding factor 1 (TRF1) (c), RNA polymerase I large subunit (RPA194) (d), upstream binding factor (UBF) (e), histones H2B (f1), H4 (f2), ubiquitin (Ub) (g), A-type lamins (h), histone demethylase JMJD2b (i), tumour suppressor p53 (j), oncoprotein c-MYC (k), β-catenin (l), STAT1 (m), α-tubulin (n), PML protein (o), and Oct3/4 (p).Back to article page