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pgenlenti flag mda5  (Addgene inc)


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    Structured Review

    Addgene inc pgenlenti flag mda5
    Pgenlenti Flag Mda5, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 78 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/pgenlenti flag mda5/product/Addgene inc
    Average 93 stars, based on 78 article reviews
    pgenlenti flag mda5 - by Bioz Stars, 2026-05
    93/100 stars

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    Image Search Results


    Figure 3. Cell-cycle arrest and apoptosis induced by the combination treatment (A and B) Flow cytometry analysis of EdU (5-ethynyl-2’-deoxyuridine) and DNA staining. H460 and H1703 cells were treated with vehicle, MYCi975 (5 μM), TMP195 (25 μM), or both for 48 h, then incubated with EdU for 2 h and stained for EdU and FxCycle Violet. Representative flow cytometry dot plots illustrating the gating strategy (A). A, G0/G1; B, S; C, G2/M. Percentages of cells in G0/G1, S, or G2/M phase are presented as mean ± SD (B). *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 calculated using one-way ANOVA followed by Tukey’s multiple comparisons test. n = 3 biological replicates. (C) Flow cytometry analysis of phosphatidylinositol (PI) and Annexin V staining. H460 and H1703 cells were treated with vehicle, MYCi975 (5 μM), TMP195 (25 μM), or both for 72 h. Representative flow cytometry dot plots illustrating the gating strategy. A, necrotic; B, late apoptotic; C, early apoptotic. (D) Percentages of cells in necrotic, late-apoptotic, or early-apoptotic status treated with vehicle, MYCi975 (5 μM), TMP195 (25 μM), or both for 24, 48, and 72 h are presented as mean ± SD. n = 3 biological replicates. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 calculated for necrotic + apoptotic cell percentages for each condition using one-way ANOVA followed by Tukey’s multiple comparisons test. V, vehicle; M, MYCi975; T, TMP195; C, combo (B and D).

    Journal: Cell reports

    Article Title: MYC plus class IIa HDAC inhibition drives mitochondrial dysfunction in non-small cell lung cancer.

    doi: 10.1016/j.celrep.2025.115722

    Figure Lengend Snippet: Figure 3. Cell-cycle arrest and apoptosis induced by the combination treatment (A and B) Flow cytometry analysis of EdU (5-ethynyl-2’-deoxyuridine) and DNA staining. H460 and H1703 cells were treated with vehicle, MYCi975 (5 μM), TMP195 (25 μM), or both for 48 h, then incubated with EdU for 2 h and stained for EdU and FxCycle Violet. Representative flow cytometry dot plots illustrating the gating strategy (A). A, G0/G1; B, S; C, G2/M. Percentages of cells in G0/G1, S, or G2/M phase are presented as mean ± SD (B). *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 calculated using one-way ANOVA followed by Tukey’s multiple comparisons test. n = 3 biological replicates. (C) Flow cytometry analysis of phosphatidylinositol (PI) and Annexin V staining. H460 and H1703 cells were treated with vehicle, MYCi975 (5 μM), TMP195 (25 μM), or both for 72 h. Representative flow cytometry dot plots illustrating the gating strategy. A, necrotic; B, late apoptotic; C, early apoptotic. (D) Percentages of cells in necrotic, late-apoptotic, or early-apoptotic status treated with vehicle, MYCi975 (5 μM), TMP195 (25 μM), or both for 24, 48, and 72 h are presented as mean ± SD. n = 3 biological replicates. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 calculated for necrotic + apoptotic cell percentages for each condition using one-way ANOVA followed by Tukey’s multiple comparisons test. V, vehicle; M, MYCi975; T, TMP195; C, combo (B and D).

    Article Snippet: Cell viability assay with MYC overexpressing H460 cells pcDNA3-cMYC (Addgene, #16011) was reverse-transfected in H460 cells using Lipofectamine 3000 Transfection Reagent (Invitrogen, #L3000001) following the manufacturer’s protocol.

    Techniques: Flow Cytometry, Staining, Incubation

    Figure 5. Combination treatment induces large-scale changes in chromatin accessibility (A) Volcano plots of ATAC-seq consensus peaks. Orange dots represent DARs with adjusted p <0.05. Each dot represents one peak. H460 cells were treated with vehicle, MYCi975 (5 μM), TMP195 (25 μM), or both for 24 h. n = 4 biological replicates. (B) Heatmaps representing ATAC-seq peaks within DARs (combo vs. vehicle) for indicated samples in H460 cells.

    Journal: Cell reports

    Article Title: MYC plus class IIa HDAC inhibition drives mitochondrial dysfunction in non-small cell lung cancer.

    doi: 10.1016/j.celrep.2025.115722

    Figure Lengend Snippet: Figure 5. Combination treatment induces large-scale changes in chromatin accessibility (A) Volcano plots of ATAC-seq consensus peaks. Orange dots represent DARs with adjusted p <0.05. Each dot represents one peak. H460 cells were treated with vehicle, MYCi975 (5 μM), TMP195 (25 μM), or both for 24 h. n = 4 biological replicates. (B) Heatmaps representing ATAC-seq peaks within DARs (combo vs. vehicle) for indicated samples in H460 cells.

    Article Snippet: Cell viability assay with MYC overexpressing H460 cells pcDNA3-cMYC (Addgene, #16011) was reverse-transfected in H460 cells using Lipofectamine 3000 Transfection Reagent (Invitrogen, #L3000001) following the manufacturer’s protocol.

    Techniques: