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dead cell reagent 7-aad  (Merck KGaA)

 
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    Merck KGaA dead cell reagent 7-aad
    Dead Cell Reagent 7 Aad, supplied by Merck KGaA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/dead+cell+reagent+7-aad/dead+cell+reagent+7+aad/pmc09334116-83-52-61
    Average 90 stars, based on 1 article reviews
    dead cell reagent 7-aad - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Multiple Displacement Amplification:

    Article Title: In Vitro Growth Inhibition, Caspase-Dependent Apoptosis, and S and G2/M Phase Arrest in Breast Cancer Cells Induced by Fluorine-Incorporated Gold I Compound, Ph3PAu[SC(OMe)=NC6H4F-3]
    Article Snippet: MDA-MB-231 and MCF-7 cells were seeded at 4 × 10 5 cells/mL into T25 flasks and incubated for 24 h. The cells were then treated with the respective IC 50 dose of the gold compound, 3F1, and incubated for a further 24 h. Treated cells were stained with MUSE Annexin V-PE and dead cell reagent 7-AAD according to the manufacturer's instructions (Merck-Millipore, USA) [ – ].

    Incubation:

    Article Title: In Vitro Growth Inhibition, Caspase-Dependent Apoptosis, and S and G2/M Phase Arrest in Breast Cancer Cells Induced by Fluorine-Incorporated Gold I Compound, Ph3PAu[SC(OMe)=NC6H4F-3]
    Article Snippet: MDA-MB-231 and MCF-7 cells were seeded at 4 × 10 5 cells/mL into T25 flasks and incubated for 24 h. The cells were then treated with the respective IC 50 dose of the gold compound, 3F1, and incubated for a further 24 h. Treated cells were stained with MUSE Annexin V-PE and dead cell reagent 7-AAD according to the manufacturer's instructions (Merck-Millipore, USA) [ – ].

    Staining:

    Article Title: In Vitro Growth Inhibition, Caspase-Dependent Apoptosis, and S and G2/M Phase Arrest in Breast Cancer Cells Induced by Fluorine-Incorporated Gold I Compound, Ph3PAu[SC(OMe)=NC6H4F-3]
    Article Snippet: MDA-MB-231 and MCF-7 cells were seeded at 4 × 10 5 cells/mL into T25 flasks and incubated for 24 h. The cells were then treated with the respective IC 50 dose of the gold compound, 3F1, and incubated for a further 24 h. Treated cells were stained with MUSE Annexin V-PE and dead cell reagent 7-AAD according to the manufacturer's instructions (Merck-Millipore, USA) [ – ].



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