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Journal: Frontiers in Pharmacology
Article Title: Cathepsin V regulates cell cycle progression and histone stability in the nucleus of breast cancer cells
doi: 10.3389/fphar.2023.1271435
Figure Lengend Snippet: Histone H3 and H4 protein expression is regulated by CTSV. ( A) Western blotting analysis of histone protein expression shows a reduction in histone H3 and H4 in CTSV depleted cells, with no impact on histones H1, H2a and H2b. (B) Confirmation of CTSV impact on histone H3 and H4 was ascertained using rescue experiments and the re-expression of CTSV in shCTSV-1 cells. GAPDH expression was used as an internal loading control and data presented is representative of at least three independent experiments.
Article Snippet: The following antibodies were used in this study; goat polyclonal CTSV (BioTechne, AF1080), goat polyclonal cyclin D1/D2 (AF4196, BioTechne), mouse monoclonal cyclin E1 (MAB68101, BioTechne), rabbit monoclonal cyclin B1 (MAB60001, BioTechne), rabbit polyclonal HDAC1 (2062S, Cell Signaling), mouse monoclonal histone H1 (NBP2-45184, BioTechne), rabbit polyclonal histone H2a (NB100-56346, BioTechne),
Techniques: Expressing, Western Blot
Journal: Cell reports
Article Title: Dissecting gene activation and chromatin remodeling dynamics in single human cells undergoing reprogramming.
doi: 10.1016/j.celrep.2024.114170
Figure Lengend Snippet: Figure 3. Global chromatin de-compaction during heterokaryon reprogramming (A) Representative Voronoi density rendering visual- izations of H2B STORM images of the somatic nu- cleus of control and heterokaryons at different time points after fusion. (B) Quantification of chromatin compaction changes during early heterokaryon reprogramming. Voronoi density values at the 95th percentile corresponding to H2B localizations from somatic nuclei of controls and heterokaryons at different time points after fusion. n = two–four biological replicates. Smaller dots represent individual values, and colored dots are the mean of biological replicates. Two-tailed t test was used to calculate p values and statistical signif- icance using the mean values of biological replicates. (C) Fold change Voronoi density relative to control. The percentage of decrease compared with control is shown for 48 h. Data correspond to the mean and SEM of two–four biological replicates. (D) Homokaryon generation strategy. hFBs were stained against CD90 using antibodies labeled with different fluorophores and fused with PEG. Fused cells containing both fluorescent markers were sor- ted as homokaryons. (E) Representative Voronoi density rendering visual- izations of H2B STORM images of the somatic nu- cleus of unfused fibroblast control and fibroblast homokaryon 48 h after fusion. (F) Voronoi density values at the 95th percentile cor- responding to H2B localizations of fibroblast nuclei at control and homokaryons at 48 h after fusion. n = one biological replicate. Smaller dots are individual values; black dots are the mean values of biological replicates. Error bars are the standard deviations. Two-tailed t test was used to calculate p values and statistical significance. Images in (A) and (E) are color-coded based on Vor- onoi density values from low (blue) to high (red).
Article Snippet: REAGENT or
Techniques: Control, Two Tailed Test, Staining, Labeling