pca plots (Qlucore Inc)
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Pca Plots, supplied by Qlucore Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 86 stars, based on 1 article reviews
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1) Product Images from "Persistent interferon signaling and clonal expansion mark early events in DNA methylation damage-induced liver cancer"
Article Title: Persistent interferon signaling and clonal expansion mark early events in DNA methylation damage-induced liver cancer
Journal: bioRxiv
doi: 10.1101/2025.10.01.679856
Figure Legend Snippet: a , Whole-cell liver lysates collected at 1 day, 5 days, and 10 weeks post-exposure were analyzed by western blot for phosho-p53. Band intensities normalized to TPS and saline WT controls. n = 4 per group (2 males, 2 females). b , Liver lysates from identical timepoints were immunoblotted for p21, normalized as above. n = 4 per group (2 males, 2 females). c , Liver lysates from identical timepoints were immunoblotted for RAD51, normalized as above. n = 4 per group (2 males, 2 females). d , e , Principal Component Analysis (PCA) of phosphoproteomics at 1 day ( d ) and 10 weeks ( e ) post-exposure displayed distinct sample clustering by treatment group and genotype. n = 4 (2 males and 2 females). f , g , Heatmaps show the most differentially expressed phosphorylated proteins at 1 day ( f ) and 10 weeks ( g ) post-exposure, identified by phosphoproteomics. DNA repair proteins are highlighted in bold ( f ). Protein selection based on multi-group ANOVA by treatment (p < 0.05), with standard deviation < 0.05; 354 total proteins ( f ), 214 total proteins ( g ). h , Phosphoproteomic quantification of gH2AX (combined S140 and S137 sites) at 1 day post-exposure. n ≥ 2 per group. i, STRING database analysis of top-expressed phosphoproteins at 1 day and 10 weeks post-exposure. Functional enrichment at 1 day highlights DNA repair clusters; 10 weeks displays enrichment for non-DNA repair biological processes from gene ontology. Statistical comparisons performed using one-way ANOVA with Šídák’s multiple comparisons test ( a – c , h ). Data are presented as mean ± s.e.m. Statistical significance: *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001. NS, not significant.
Techniques Used: Western Blot, Saline, Phospho-proteomics, Selection, Standard Deviation, Functional Assay
Figure Legend Snippet: a , PCA of Mgmt −/− liver samples collected at days 1, 2, and 5 post-saline or NDMA exposure shows clear clustering separation by treatment group. RNA was extracted from liver tissue and analyzed by RNA-seq; n ≥ 7 per group (males and females combined). b , Bar graphs depict the number of differentially expressed RNA transcripts (up- and downregulated) in WT and Mgmt −/− liver following NDMA exposure across indicated timepoints. c , Venn diagrams compare overlap of significantly up- and downregulated genes across genotypes and timepoints. d , Pathway enrichment analysis of persistently up- and downregulated genes (intersected across all timepoints from panel c , red circles) in Mgmt −/− samples using Enrichr for MSigDB Hallmark gene sets. The top 8 pathways are displayed, ranked by Fisher exact test p-value. Pathways involved in IFN response are marked with an asterisk (*). e , Volcano plots display the most differentially expressed genes in Mgmt −/− livers comparing NDMA vs saline treatment at 1 day, 5 days, and 10 weeks. Plots show –log 10 p-value versus log 2 fold change. Genes from the GSEA Hallmark p53 pathway are circled in red or black; Cyp2e1 downregulation is circled in blue. f , i , Bar graphs quantify the number of up- and downregulated genes within the pre-curated IFN ( f ) and DNA repair ( i ) gene lists, comparing NDMA effects between WT and Mgmt −/− across the time course. g , h , Heatmaps show expression profiles for curated IFN response genes ( g ) and DNA repair genes ( h ) in response to NDMA treatment in WT and Mgmt −/− livers at days 1, 2, and 5 post-exposure. Color scale reflects relative gene expression intensity. Statistical analysis: All comparisons use thresholds of adjusted p-value < 0.05 and absolute log 2 fold change > 0.58 ( b – i ).
Techniques Used: Saline, RNA Sequencing, Expressing, Gene Expression

