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rabbit α h3k4me3  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc rabbit α h3k4me3
    Rabbit α H3k4me3, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 941 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/%CE%B1+histone+h3/Tri-Methyl-Histone+H3+(Lys4)+Rabbit+mAb/pm41841741-359-131-133
    Average 97 stars, based on 941 article reviews
    rabbit α h3k4me3 - by Bioz Stars, 2026-09
    97/100 stars

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    Related Articles

    Western Blot:

    Article Title: A Macrohistone Variant Links Dynamic Chromatin Compaction to BRCA1-Dependent Genome Maintenance
    Article Snippet: .. The following antibodies were used for immunoblotting: α−p-RPA (S4/S8, Bethyl), α−RPA2 (Millipore NA19), α−histone H3 (Cell signaling 9715), α−histone H2A (Abcam ab15653), α−H3K9 (me)2 (Abcam ab1220), α−macroH2A1 (Millipore 07-219), α−γ−H2AX (Millipore 05-636), α−53BP1 (Santa Cruz sc22760), and α−β−tubulin (Cell signaling 2146), α−HA (Santa Cruz sc805) and α−GFP (Santa Cruz sc9996). ..

    Article Title: A mouse monoclonal antibody against influenza C virus attenuates acetaminophen-induced liver injury in mice.
    Article Snippet: .. For western blotting, α-mouse ACAA2 (ab128911; Abcam, Cambridge, UK), α-GAPDH (#5174; Cell Signaling Technology, Danvers, MA, USA), α-HSP60 (#12165; Cell Signaling Technology), α-histone H3 (#4499; Cell Signaling Technology), α-Flag M2 (F1804; Sigma-Aldrich, St. Louis, MO, USA), and α-mouse albumin (#4929; Cell Signaling Technology) polyclonal antibodies (pAbs) were used as the primary antibodies. .. Horseradish peroxidase (HRP)-conjugated secondary antibodies against mouse and rabbit IgG were purchased from Bio-Rad (Hercules, CA, USA).

    Article Title: A mouse monoclonal antibody against influenza C virus attenuates acetaminophen-induced liver injury in mice
    Article Snippet: .. For western blotting, α-mouse ACAA2 (ab128911; Abcam, Cambridge, UK), α-GAPDH (#5174; Cell Signaling Technology, Danvers, MA, USA), α-HSP60 (#12165; Cell Signaling Technology), α-histone H3 (#4499; Cell Signaling Technology), α-Flag M2 (F1804; Sigma-Aldrich, St. Louis, MO, USA), and α-mouse albumin (#4929; Cell Signaling Technology) polyclonal antibodies (pAbs) were used as the primary antibodies. .. Horseradish peroxidase (HRP)-conjugated secondary antibodies against mouse and rabbit IgG were purchased from Bio-Rad (Hercules, CA, USA).

    Incubation:

    Article Title: A Class of Environmental and Endogenous Toxins Induces BRCA2 Haploinsufficiency and Genome Instability
    Article Snippet: .. Membranes were incubated with primary antibodies (α-BRCA2 (Merck Millipore, ab-1, 1:500), α-BRCA1 (Santa Cruz, C-20, 1:200), α-PALB2 (Bethyl A301-246A, 1:1000), α-RAD51 (GeneTex, 14B4, 1:500), α-p-ATM (S1981) (Abcam, ab81292, 1:1000), α-ATM (Sigma, A1106, 1:500), α-p-ATR (T1989) (GeneTex, GTX128145, 1:500), α-ATR (Bethyl, A300-137A, 1:10000), α-LC3B (Cell Signaling, D11, 1:1000), α-FLAG (Sigma, M2, 1:500), α-polyubiquitin (Enzo, FK2, 1:1000), α-Hsp90 (Cell Signaling, C45G5, 1:1000), α-β-actin (Sigma, A5441, 1:10000), α-XRCC3 (Oncogene, PC691, 1:5000), α-FANCI (Abcam, ab15344, 1:2000), α-Ku80 (Santa Cruz, sc-1485, 1:500), α-Ku70 (Abcam, ab3114, 1:500), α-XRCC4 (Abcam, ab145, 1:2000), α-mCherry (Novus Biologicals, NBP1-96752, 1:2000), α-Histone H3 (Cell Signaling, #9715, 1:1000, α-c-Myc (Santa Cruz, sc-40, 1:500), α-PLK1 (ThermoFisher, 331700, 1:1000), α-Aurora B (Abcam, ab2254, 1:1000), α-TXNL1 (Abcam, ab188328, 1:2000), α-JAK1 (Santa Cruz, sc-376996, 1:500)) overnight at 4°C followed by washing in 0.1%Tween/TBS. ..



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    Cell Signaling Technology Inc α h3k27me3
    A Experimental schematic. Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . B Profile heatmap of H3K4me3, H3K27ac, and <t>H3K27me3</t> -3Kb upstream and 3Kb downstream of the TSS. D458 (parent), D458IR were treated with IDH305 (7μM) or GSK321 (1μM) for 48 hours. C Annotation of percent H3K27ac, H3K4me3, and H3K27me3 increased and decreased peak occupancy in D458IR(resistant) compared to D458(parent). (Below) Increased and decreased peak occupancy in D458IR(resistant) treated with IDH305 compared to DMSO treated D458IR. D Summary of H3K4me3, H3K27ac, and H3K27me3 peak occupancy changes at the promoter and distal intergenic and intron regions. E Schematic representation of ( F and G) . Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . F Scatter plots of D458IR/D458 Log 2 FC ratio compared to D458IR + IDH1i/D458IR for H3K27ac (correlation coefficient = -.58, p = 2.2e−16) and G H3K27me3 (correlation coefficient = -.35, p = 5.758e-08). Two-tailed Pearson’s correlation analysis between assigned peaks in (IR/Ctrl) and (IDH1i+IR/IR). P-value represents one sample proportions test. H Scatter plots of D458IR/D458 Log 2 FC ratio of H3K4me3 compared to H3K27me3. DEGs from scRNA-seq is overlayed on gene identified peaks, red genes up and blue genes downregulated. Green box indicates increased peak occupancy for H3K4me3 and H3K27me3. I Gene set enrichment analysis of dual occupied H3K4me3/H3K27me3 peaks. The significance of enrichment is reported as(-Log10(Pval)). J Scatter plots of D458IR + IDH1i/D458IR Log 2 FC H3K4me3 compared to H3K27me3. K Genome browser view of representative gene loci from the progenitor_photoreceptor signature. Chromatin accessibility (ATAC-seq), H3K4me3, H3K27ac, H3K27me3 occupancy in D458 (sensitive), D458IR (IR-resistant), D458IR (IR-resistant) + IDH305 (7μM) or + GSK321 (1μM) are displayed. Scale for each histone mark is shown. All CUT and RUN experiments represent a n = 2. See also Supplementary Fig. .
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    Cell Signaling Technology Inc α h3k27ac
    A Experimental schematic. Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . B Profile heatmap of H3K4me3, <t>H3K27ac,</t> and H3K27me3 -3Kb upstream and 3Kb downstream of the TSS. D458 (parent), D458IR were treated with IDH305 (7μM) or GSK321 (1μM) for 48 hours. C Annotation of percent H3K27ac, H3K4me3, and H3K27me3 increased and decreased peak occupancy in D458IR(resistant) compared to D458(parent). (Below) Increased and decreased peak occupancy in D458IR(resistant) treated with IDH305 compared to DMSO treated D458IR. D Summary of H3K4me3, H3K27ac, and H3K27me3 peak occupancy changes at the promoter and distal intergenic and intron regions. E Schematic representation of ( F and G) . Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . F Scatter plots of D458IR/D458 Log 2 FC ratio compared to D458IR + IDH1i/D458IR for H3K27ac (correlation coefficient = -.58, p = 2.2e−16) and G H3K27me3 (correlation coefficient = -.35, p = 5.758e-08). Two-tailed Pearson’s correlation analysis between assigned peaks in (IR/Ctrl) and (IDH1i+IR/IR). P-value represents one sample proportions test. H Scatter plots of D458IR/D458 Log 2 FC ratio of H3K4me3 compared to H3K27me3. DEGs from scRNA-seq is overlayed on gene identified peaks, red genes up and blue genes downregulated. Green box indicates increased peak occupancy for H3K4me3 and H3K27me3. I Gene set enrichment analysis of dual occupied H3K4me3/H3K27me3 peaks. The significance of enrichment is reported as(-Log10(Pval)). J Scatter plots of D458IR + IDH1i/D458IR Log 2 FC H3K4me3 compared to H3K27me3. K Genome browser view of representative gene loci from the progenitor_photoreceptor signature. Chromatin accessibility (ATAC-seq), H3K4me3, H3K27ac, H3K27me3 occupancy in D458 (sensitive), D458IR (IR-resistant), D458IR (IR-resistant) + IDH305 (7μM) or + GSK321 (1μM) are displayed. Scale for each histone mark is shown. All CUT and RUN experiments represent a n = 2. See also Supplementary Fig. .
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    A Experimental schematic. Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . B Profile heatmap of H3K4me3, <t>H3K27ac,</t> and H3K27me3 -3Kb upstream and 3Kb downstream of the TSS. D458 (parent), D458IR were treated with IDH305 (7μM) or GSK321 (1μM) for 48 hours. C Annotation of percent H3K27ac, H3K4me3, and H3K27me3 increased and decreased peak occupancy in D458IR(resistant) compared to D458(parent). (Below) Increased and decreased peak occupancy in D458IR(resistant) treated with IDH305 compared to DMSO treated D458IR. D Summary of H3K4me3, H3K27ac, and H3K27me3 peak occupancy changes at the promoter and distal intergenic and intron regions. E Schematic representation of ( F and G) . Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . F Scatter plots of D458IR/D458 Log 2 FC ratio compared to D458IR + IDH1i/D458IR for H3K27ac (correlation coefficient = -.58, p = 2.2e−16) and G H3K27me3 (correlation coefficient = -.35, p = 5.758e-08). Two-tailed Pearson’s correlation analysis between assigned peaks in (IR/Ctrl) and (IDH1i+IR/IR). P-value represents one sample proportions test. H Scatter plots of D458IR/D458 Log 2 FC ratio of H3K4me3 compared to H3K27me3. DEGs from scRNA-seq is overlayed on gene identified peaks, red genes up and blue genes downregulated. Green box indicates increased peak occupancy for H3K4me3 and H3K27me3. I Gene set enrichment analysis of dual occupied H3K4me3/H3K27me3 peaks. The significance of enrichment is reported as(-Log10(Pval)). J Scatter plots of D458IR + IDH1i/D458IR Log 2 FC H3K4me3 compared to H3K27me3. K Genome browser view of representative gene loci from the progenitor_photoreceptor signature. Chromatin accessibility (ATAC-seq), H3K4me3, H3K27ac, H3K27me3 occupancy in D458 (sensitive), D458IR (IR-resistant), D458IR (IR-resistant) + IDH305 (7μM) or + GSK321 (1μM) are displayed. Scale for each histone mark is shown. All CUT and RUN experiments represent a n = 2. See also Supplementary Fig. .
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    A Experimental schematic. Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . B Profile heatmap of H3K4me3, <t>H3K27ac,</t> and H3K27me3 -3Kb upstream and 3Kb downstream of the TSS. D458 (parent), D458IR were treated with IDH305 (7μM) or GSK321 (1μM) for 48 hours. C Annotation of percent H3K27ac, H3K4me3, and H3K27me3 increased and decreased peak occupancy in D458IR(resistant) compared to D458(parent). (Below) Increased and decreased peak occupancy in D458IR(resistant) treated with IDH305 compared to DMSO treated D458IR. D Summary of H3K4me3, H3K27ac, and H3K27me3 peak occupancy changes at the promoter and distal intergenic and intron regions. E Schematic representation of ( F and G) . Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . F Scatter plots of D458IR/D458 Log 2 FC ratio compared to D458IR + IDH1i/D458IR for H3K27ac (correlation coefficient = -.58, p = 2.2e−16) and G H3K27me3 (correlation coefficient = -.35, p = 5.758e-08). Two-tailed Pearson’s correlation analysis between assigned peaks in (IR/Ctrl) and (IDH1i+IR/IR). P-value represents one sample proportions test. H Scatter plots of D458IR/D458 Log 2 FC ratio of H3K4me3 compared to H3K27me3. DEGs from scRNA-seq is overlayed on gene identified peaks, red genes up and blue genes downregulated. Green box indicates increased peak occupancy for H3K4me3 and H3K27me3. I Gene set enrichment analysis of dual occupied H3K4me3/H3K27me3 peaks. The significance of enrichment is reported as(-Log10(Pval)). J Scatter plots of D458IR + IDH1i/D458IR Log 2 FC H3K4me3 compared to H3K27me3. K Genome browser view of representative gene loci from the progenitor_photoreceptor signature. Chromatin accessibility (ATAC-seq), H3K4me3, H3K27ac, H3K27me3 occupancy in D458 (sensitive), D458IR (IR-resistant), D458IR (IR-resistant) + IDH305 (7μM) or + GSK321 (1μM) are displayed. Scale for each histone mark is shown. All CUT and RUN experiments represent a n = 2. See also Supplementary Fig. .
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    Image Search Results


    A Experimental schematic. Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . B Profile heatmap of H3K4me3, H3K27ac, and H3K27me3 -3Kb upstream and 3Kb downstream of the TSS. D458 (parent), D458IR were treated with IDH305 (7μM) or GSK321 (1μM) for 48 hours. C Annotation of percent H3K27ac, H3K4me3, and H3K27me3 increased and decreased peak occupancy in D458IR(resistant) compared to D458(parent). (Below) Increased and decreased peak occupancy in D458IR(resistant) treated with IDH305 compared to DMSO treated D458IR. D Summary of H3K4me3, H3K27ac, and H3K27me3 peak occupancy changes at the promoter and distal intergenic and intron regions. E Schematic representation of ( F and G) . Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . F Scatter plots of D458IR/D458 Log 2 FC ratio compared to D458IR + IDH1i/D458IR for H3K27ac (correlation coefficient = -.58, p = 2.2e−16) and G H3K27me3 (correlation coefficient = -.35, p = 5.758e-08). Two-tailed Pearson’s correlation analysis between assigned peaks in (IR/Ctrl) and (IDH1i+IR/IR). P-value represents one sample proportions test. H Scatter plots of D458IR/D458 Log 2 FC ratio of H3K4me3 compared to H3K27me3. DEGs from scRNA-seq is overlayed on gene identified peaks, red genes up and blue genes downregulated. Green box indicates increased peak occupancy for H3K4me3 and H3K27me3. I Gene set enrichment analysis of dual occupied H3K4me3/H3K27me3 peaks. The significance of enrichment is reported as(-Log10(Pval)). J Scatter plots of D458IR + IDH1i/D458IR Log 2 FC H3K4me3 compared to H3K27me3. K Genome browser view of representative gene loci from the progenitor_photoreceptor signature. Chromatin accessibility (ATAC-seq), H3K4me3, H3K27ac, H3K27me3 occupancy in D458 (sensitive), D458IR (IR-resistant), D458IR (IR-resistant) + IDH305 (7μM) or + GSK321 (1μM) are displayed. Scale for each histone mark is shown. All CUT and RUN experiments represent a n = 2. See also Supplementary Fig. .

    Journal: Nature Communications

    Article Title: Single-cell multi-omics identifies metabolism-linked epigenetic reprogramming as a driver of therapy-resistant medulloblastoma

    doi: 10.1038/s41467-025-65466-9

    Figure Lengend Snippet: A Experimental schematic. Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . B Profile heatmap of H3K4me3, H3K27ac, and H3K27me3 -3Kb upstream and 3Kb downstream of the TSS. D458 (parent), D458IR were treated with IDH305 (7μM) or GSK321 (1μM) for 48 hours. C Annotation of percent H3K27ac, H3K4me3, and H3K27me3 increased and decreased peak occupancy in D458IR(resistant) compared to D458(parent). (Below) Increased and decreased peak occupancy in D458IR(resistant) treated with IDH305 compared to DMSO treated D458IR. D Summary of H3K4me3, H3K27ac, and H3K27me3 peak occupancy changes at the promoter and distal intergenic and intron regions. E Schematic representation of ( F and G) . Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . F Scatter plots of D458IR/D458 Log 2 FC ratio compared to D458IR + IDH1i/D458IR for H3K27ac (correlation coefficient = -.58, p = 2.2e−16) and G H3K27me3 (correlation coefficient = -.35, p = 5.758e-08). Two-tailed Pearson’s correlation analysis between assigned peaks in (IR/Ctrl) and (IDH1i+IR/IR). P-value represents one sample proportions test. H Scatter plots of D458IR/D458 Log 2 FC ratio of H3K4me3 compared to H3K27me3. DEGs from scRNA-seq is overlayed on gene identified peaks, red genes up and blue genes downregulated. Green box indicates increased peak occupancy for H3K4me3 and H3K27me3. I Gene set enrichment analysis of dual occupied H3K4me3/H3K27me3 peaks. The significance of enrichment is reported as(-Log10(Pval)). J Scatter plots of D458IR + IDH1i/D458IR Log 2 FC H3K4me3 compared to H3K27me3. K Genome browser view of representative gene loci from the progenitor_photoreceptor signature. Chromatin accessibility (ATAC-seq), H3K4me3, H3K27ac, H3K27me3 occupancy in D458 (sensitive), D458IR (IR-resistant), D458IR (IR-resistant) + IDH305 (7μM) or + GSK321 (1μM) are displayed. Scale for each histone mark is shown. All CUT and RUN experiments represent a n = 2. See also Supplementary Fig. .

    Article Snippet: Antibodies against α-H3K4me3 and IgG controls were validated antibodies from EpiCypher. α-H3K27me3 (Cell Signaling technologies, #9733) and α-H3K27ac (Cell signaling technologies, #8173).

    Techniques: Two Tailed Test

    A Experimental schematic. Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . B Profile heatmap of H3K4me3, H3K27ac, and H3K27me3 -3Kb upstream and 3Kb downstream of the TSS. D458 (parent), D458IR were treated with IDH305 (7μM) or GSK321 (1μM) for 48 hours. C Annotation of percent H3K27ac, H3K4me3, and H3K27me3 increased and decreased peak occupancy in D458IR(resistant) compared to D458(parent). (Below) Increased and decreased peak occupancy in D458IR(resistant) treated with IDH305 compared to DMSO treated D458IR. D Summary of H3K4me3, H3K27ac, and H3K27me3 peak occupancy changes at the promoter and distal intergenic and intron regions. E Schematic representation of ( F and G) . Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . F Scatter plots of D458IR/D458 Log 2 FC ratio compared to D458IR + IDH1i/D458IR for H3K27ac (correlation coefficient = -.58, p = 2.2e−16) and G H3K27me3 (correlation coefficient = -.35, p = 5.758e-08). Two-tailed Pearson’s correlation analysis between assigned peaks in (IR/Ctrl) and (IDH1i+IR/IR). P-value represents one sample proportions test. H Scatter plots of D458IR/D458 Log 2 FC ratio of H3K4me3 compared to H3K27me3. DEGs from scRNA-seq is overlayed on gene identified peaks, red genes up and blue genes downregulated. Green box indicates increased peak occupancy for H3K4me3 and H3K27me3. I Gene set enrichment analysis of dual occupied H3K4me3/H3K27me3 peaks. The significance of enrichment is reported as(-Log10(Pval)). J Scatter plots of D458IR + IDH1i/D458IR Log 2 FC H3K4me3 compared to H3K27me3. K Genome browser view of representative gene loci from the progenitor_photoreceptor signature. Chromatin accessibility (ATAC-seq), H3K4me3, H3K27ac, H3K27me3 occupancy in D458 (sensitive), D458IR (IR-resistant), D458IR (IR-resistant) + IDH305 (7μM) or + GSK321 (1μM) are displayed. Scale for each histone mark is shown. All CUT and RUN experiments represent a n = 2. See also Supplementary Fig. .

    Journal: Nature Communications

    Article Title: Single-cell multi-omics identifies metabolism-linked epigenetic reprogramming as a driver of therapy-resistant medulloblastoma

    doi: 10.1038/s41467-025-65466-9

    Figure Lengend Snippet: A Experimental schematic. Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . B Profile heatmap of H3K4me3, H3K27ac, and H3K27me3 -3Kb upstream and 3Kb downstream of the TSS. D458 (parent), D458IR were treated with IDH305 (7μM) or GSK321 (1μM) for 48 hours. C Annotation of percent H3K27ac, H3K4me3, and H3K27me3 increased and decreased peak occupancy in D458IR(resistant) compared to D458(parent). (Below) Increased and decreased peak occupancy in D458IR(resistant) treated with IDH305 compared to DMSO treated D458IR. D Summary of H3K4me3, H3K27ac, and H3K27me3 peak occupancy changes at the promoter and distal intergenic and intron regions. E Schematic representation of ( F and G) . Created in BioRender. Vibhakar, R. (2025) https://BioRender.com/5nsqycy . F Scatter plots of D458IR/D458 Log 2 FC ratio compared to D458IR + IDH1i/D458IR for H3K27ac (correlation coefficient = -.58, p = 2.2e−16) and G H3K27me3 (correlation coefficient = -.35, p = 5.758e-08). Two-tailed Pearson’s correlation analysis between assigned peaks in (IR/Ctrl) and (IDH1i+IR/IR). P-value represents one sample proportions test. H Scatter plots of D458IR/D458 Log 2 FC ratio of H3K4me3 compared to H3K27me3. DEGs from scRNA-seq is overlayed on gene identified peaks, red genes up and blue genes downregulated. Green box indicates increased peak occupancy for H3K4me3 and H3K27me3. I Gene set enrichment analysis of dual occupied H3K4me3/H3K27me3 peaks. The significance of enrichment is reported as(-Log10(Pval)). J Scatter plots of D458IR + IDH1i/D458IR Log 2 FC H3K4me3 compared to H3K27me3. K Genome browser view of representative gene loci from the progenitor_photoreceptor signature. Chromatin accessibility (ATAC-seq), H3K4me3, H3K27ac, H3K27me3 occupancy in D458 (sensitive), D458IR (IR-resistant), D458IR (IR-resistant) + IDH305 (7μM) or + GSK321 (1μM) are displayed. Scale for each histone mark is shown. All CUT and RUN experiments represent a n = 2. See also Supplementary Fig. .

    Article Snippet: Antibodies against α-H3K4me3 and IgG controls were validated antibodies from EpiCypher. α-H3K27me3 (Cell Signaling technologies, #9733) and α-H3K27ac (Cell signaling technologies, #8173).

    Techniques: Two Tailed Test