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rabbit monoclonal anti cleaved caspase 3 asp175 d3e9 ab  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit monoclonal anti cleaved caspase 3 asp175 d3e9 ab
    (A) Measurements of the transcriptional activities of HA-MYC WT and HA-MYC ΔC in HeLa cells using the dual MYC reporter system (mean ± SD, n=3 independent experiments, One-way ANOVA). (B) Quantitation of apoptosis induced by transient expression of HA-MYC WT or HA-MYC ΔC in serum-starved NIH3T3 cells by flow cytometry using anti-cleaved <t>caspase</t> <t>3</t> Abs (mean ± SD, n=3 independent experiments, One-way ANOVA). (C) Detection of HA-MYC expression in serum-starved NIH3T3 cells by immunoblotting (representative images of four independent experiments). (E) Quantitation of apoptosis induced by transient expression of HA-MYC ΔC and its deletion mutants in serum-starved NIH3T3 cells by flow cytometry using anti-cleaved caspase 3 Abs. The results are normalized by their expression levels (mean ± SD, n=4 independent experiments, One-way ANOVA).
    Rabbit Monoclonal Anti Cleaved Caspase 3 Asp175 D3e9 Ab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 301 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit monoclonal anti cleaved caspase 3 asp175 d3e9 ab/product/Cell Signaling Technology Inc
    Average 96 stars, based on 301 article reviews
    rabbit monoclonal anti cleaved caspase 3 asp175 d3e9 ab - by Bioz Stars, 2026-05
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    1) Product Images from "c-MYC is an aggregation-prone, amyloidogenic protein"

    Article Title: c-MYC is an aggregation-prone, amyloidogenic protein

    Journal: bioRxiv

    doi: 10.64898/2026.03.12.711438

    (A) Measurements of the transcriptional activities of HA-MYC WT and HA-MYC ΔC in HeLa cells using the dual MYC reporter system (mean ± SD, n=3 independent experiments, One-way ANOVA). (B) Quantitation of apoptosis induced by transient expression of HA-MYC WT or HA-MYC ΔC in serum-starved NIH3T3 cells by flow cytometry using anti-cleaved caspase 3 Abs (mean ± SD, n=3 independent experiments, One-way ANOVA). (C) Detection of HA-MYC expression in serum-starved NIH3T3 cells by immunoblotting (representative images of four independent experiments). (E) Quantitation of apoptosis induced by transient expression of HA-MYC ΔC and its deletion mutants in serum-starved NIH3T3 cells by flow cytometry using anti-cleaved caspase 3 Abs. The results are normalized by their expression levels (mean ± SD, n=4 independent experiments, One-way ANOVA).
    Figure Legend Snippet: (A) Measurements of the transcriptional activities of HA-MYC WT and HA-MYC ΔC in HeLa cells using the dual MYC reporter system (mean ± SD, n=3 independent experiments, One-way ANOVA). (B) Quantitation of apoptosis induced by transient expression of HA-MYC WT or HA-MYC ΔC in serum-starved NIH3T3 cells by flow cytometry using anti-cleaved caspase 3 Abs (mean ± SD, n=3 independent experiments, One-way ANOVA). (C) Detection of HA-MYC expression in serum-starved NIH3T3 cells by immunoblotting (representative images of four independent experiments). (E) Quantitation of apoptosis induced by transient expression of HA-MYC ΔC and its deletion mutants in serum-starved NIH3T3 cells by flow cytometry using anti-cleaved caspase 3 Abs. The results are normalized by their expression levels (mean ± SD, n=4 independent experiments, One-way ANOVA).

    Techniques Used: Quantitation Assay, Expressing, Flow Cytometry, Western Blot



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    (A) Measurements of the transcriptional activities of HA-MYC WT and HA-MYC ΔC in HeLa cells using the dual MYC reporter system (mean ± SD, n=3 independent experiments, One-way ANOVA). (B) Quantitation of apoptosis induced by transient expression of HA-MYC WT or HA-MYC ΔC in serum-starved NIH3T3 cells by flow cytometry using anti-cleaved <t>caspase</t> <t>3</t> Abs (mean ± SD, n=3 independent experiments, One-way ANOVA). (C) Detection of HA-MYC expression in serum-starved NIH3T3 cells by immunoblotting (representative images of four independent experiments). (E) Quantitation of apoptosis induced by transient expression of HA-MYC ΔC and its deletion mutants in serum-starved NIH3T3 cells by flow cytometry using anti-cleaved caspase 3 Abs. The results are normalized by their expression levels (mean ± SD, n=4 independent experiments, One-way ANOVA).
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    (A) Measurements of the transcriptional activities of HA-MYC WT and HA-MYC ΔC in HeLa cells using the dual MYC reporter system (mean ± SD, n=3 independent experiments, One-way ANOVA). (B) Quantitation of apoptosis induced by transient expression of HA-MYC WT or HA-MYC ΔC in serum-starved NIH3T3 cells by flow cytometry using anti-cleaved caspase 3 Abs (mean ± SD, n=3 independent experiments, One-way ANOVA). (C) Detection of HA-MYC expression in serum-starved NIH3T3 cells by immunoblotting (representative images of four independent experiments). (E) Quantitation of apoptosis induced by transient expression of HA-MYC ΔC and its deletion mutants in serum-starved NIH3T3 cells by flow cytometry using anti-cleaved caspase 3 Abs. The results are normalized by their expression levels (mean ± SD, n=4 independent experiments, One-way ANOVA).

    Journal: bioRxiv

    Article Title: c-MYC is an aggregation-prone, amyloidogenic protein

    doi: 10.64898/2026.03.12.711438

    Figure Lengend Snippet: (A) Measurements of the transcriptional activities of HA-MYC WT and HA-MYC ΔC in HeLa cells using the dual MYC reporter system (mean ± SD, n=3 independent experiments, One-way ANOVA). (B) Quantitation of apoptosis induced by transient expression of HA-MYC WT or HA-MYC ΔC in serum-starved NIH3T3 cells by flow cytometry using anti-cleaved caspase 3 Abs (mean ± SD, n=3 independent experiments, One-way ANOVA). (C) Detection of HA-MYC expression in serum-starved NIH3T3 cells by immunoblotting (representative images of four independent experiments). (E) Quantitation of apoptosis induced by transient expression of HA-MYC ΔC and its deletion mutants in serum-starved NIH3T3 cells by flow cytometry using anti-cleaved caspase 3 Abs. The results are normalized by their expression levels (mean ± SD, n=4 independent experiments, One-way ANOVA).

    Article Snippet: All antibodies were purchased commercially, including rabbit polyclonal anti-amyloid oligomer (A11) Ab (cat#SPC-506, StressMarq Biosciences Inc.), rabbit monoclonal anti-c-MYC/N-MYC (D3N8F) Ab (cat#13987, Cell Signaling Technology), rabbit monoclonal ani-MAX (E6F6Y) Ab (cat#17471, Cell Signaling Technology), mouse monoclonal anti-HSC/HSP70 (W27) Ab (cat#sc-24, Santa Cruz Biotechnology Inc.), mouse monoclonal anti-HSP90α/β (F-8) Ab (cat#sc-13119, Santa Cruz Biotechnology Inc.), rabbit monoclonal anti-cleaved caspase 3 (Asp175) (D3E9) Ab (cat#9579, Cell Signaling Technology), goat polyclonal anti-c-MYC Ab (cat#AF3696, R&D Systems Inc.), mouse monoclonal anti-HA Ab (cat#901513, BioLegend Inc.), mouse monoclonal anti-βActin (GT5512) Ab (cat#GTX629630, GeneTex Inc.), normal rabbit IgG (cat#02-6102,ThermoFisher Scientific Inc.), Peroxidase AffiniPure Goat Anti-Rabbit IgG (H+L) (cat#111-035-144, Jackson ImmunoResearch Inc.), Peroxidase AffiniPure Goat Anti-Mouse IgG (H+L) (cat#115-035-003, Jackson ImmunoResearch Inc.), and Peroxidase IgG Fraction Monoclonal Mouse Anti-Goat IgG, light chain specific (cat#205-032-176, Jackson ImmunoResearch Inc.).

    Techniques: Quantitation Assay, Expressing, Flow Cytometry, Western Blot