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propidium iodide/rnase staining solution (cell signaling technology, 4087s)  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc propidium iodide/rnase staining solution (cell signaling technology, 4087s)
    Propidium Iodide/Rnase Staining Solution (Cell Signaling Technology, 4087s), supplied by Cell Signaling Technology Inc, 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/result/propidium iodide/rnase staining solution (cell signaling technology, 4087s)/product/Cell Signaling Technology Inc
    Average 90 stars, based on 1 article reviews
    propidium iodide/rnase staining solution (cell signaling technology, 4087s) - by Bioz Stars, 2026-03
    90/100 stars

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    Cell populations in different stages (live, apoptotic, and necrotic) following the extract treatment (EAE) and (CSE) of MCF-7 cells for 48 h and evaluated by double staining in Annexin <t>V-FITC/propidium</t> iodide using a flow cytometric assay. The data are presented as mean values ± SD based on three replicates ( n = 3). Significance was determined by comparing the events from each respective control, with differences considered significant at * p > 0.05; ** p < 0.01; and *** p < 0.001.
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    pi rnase staining solution  (Cell Signaling Technology Inc)
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    Cell populations in different stages (live, apoptotic, and necrotic) following the extract treatment (EAE) and (CSE) of MCF-7 cells for 48 h and evaluated by double staining in Annexin <t>V-FITC/propidium</t> iodide using a flow cytometric assay. The data are presented as mean values ± SD based on three replicates ( n = 3). Significance was determined by comparing the events from each respective control, with differences considered significant at * p > 0.05; ** p < 0.01; and *** p < 0.001.
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    Cell populations in different stages (live, apoptotic, and necrotic) following the extract treatment (EAE) and (CSE) of MCF-7 cells for 48 h and evaluated by double staining in Annexin V-FITC/propidium iodide using a flow cytometric assay. The data are presented as mean values ± SD based on three replicates ( n = 3). Significance was determined by comparing the events from each respective control, with differences considered significant at * p > 0.05; ** p < 0.01; and *** p < 0.001.

    Journal: ACS Omega

    Article Title: Exploring the Metabolic Profiling and Anticancer Activities of Red Sea Sponges Echinodictyum asperum and Callyspongia siphonella against Human Breast Cancer Cells: A Comparative Study

    doi: 10.1021/acsomega.4c10202

    Figure Lengend Snippet: Cell populations in different stages (live, apoptotic, and necrotic) following the extract treatment (EAE) and (CSE) of MCF-7 cells for 48 h and evaluated by double staining in Annexin V-FITC/propidium iodide using a flow cytometric assay. The data are presented as mean values ± SD based on three replicates ( n = 3). Significance was determined by comparing the events from each respective control, with differences considered significant at * p > 0.05; ** p < 0.01; and *** p < 0.001.

    Article Snippet: Following the washing steps, the cells were stained with 100 μL of propidium iodide (PI) solution containing RNase (Cell Signaling Technology; Boston, MA).

    Techniques: Double Staining, Flow Cytometry, Control

    Cell populations in different stages (live, apoptotic, and necrotic) following the extract treatment (EAE) and (CSE) of MDA-MB-231 cells for 48 h and evaluated by double staining in Annexin V-FITC/propidium iodide using a flow cytometric assay. The data are presented as mean values ± SD based on three replicates ( n = 3). Significance was determined by comparing the events from each respective control, with differences considered significant at * p > 0.05; ** p < 0.01; and *** p < 0.001.

    Journal: ACS Omega

    Article Title: Exploring the Metabolic Profiling and Anticancer Activities of Red Sea Sponges Echinodictyum asperum and Callyspongia siphonella against Human Breast Cancer Cells: A Comparative Study

    doi: 10.1021/acsomega.4c10202

    Figure Lengend Snippet: Cell populations in different stages (live, apoptotic, and necrotic) following the extract treatment (EAE) and (CSE) of MDA-MB-231 cells for 48 h and evaluated by double staining in Annexin V-FITC/propidium iodide using a flow cytometric assay. The data are presented as mean values ± SD based on three replicates ( n = 3). Significance was determined by comparing the events from each respective control, with differences considered significant at * p > 0.05; ** p < 0.01; and *** p < 0.001.

    Article Snippet: Following the washing steps, the cells were stained with 100 μL of propidium iodide (PI) solution containing RNase (Cell Signaling Technology; Boston, MA).

    Techniques: Double Staining, Flow Cytometry, Control