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propidium iodide pi dyes  (MedChemExpress)


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    MedChemExpress propidium iodide pi dyes
    Propidium Iodide Pi Dyes, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 98/100, based on 259 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/propidium+iodide+pi+dyes/Propidium/pmc13068572-67-21-25
    Average 98 stars, based on 259 article reviews
    propidium iodide pi dyes - by Bioz Stars, 2026-09
    98/100 stars

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    other:

    Article Title: New combination therapy of praziquantel and Lactobacillus plantarum for enhancing the treatment of clonorchiasis in mice
    Article Snippet: To differentiate between viable and non-viable larvae, juvenile worms were co-stained with 2.5 μg/mL of fluorescein diacetate and 5 μg/mL of propidium iodide (PI) dyes (MCE, New Jersey, USA).

    Article Title: New combination therapy of praziquantel and Lactobacillus plantarum for enhancing the treatment of clonorchiasis in mice
    Article Snippet: To differentiate between viable and non-viable larvae, juvenile worms were co-stained with 2.5 μg/mL of fluorescein diacetate and 5 μg/mL of propidium iodide (PI) dyes (MCE, New Jersey, USA).



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    Image Search Results


    Co-administration of gemcitabine and BD B10 induced apoptosis pathway in Panc1 cells. Apoptosis was analysed using multiple methods: (a) AO/PI doubling staining was applied to assess morphological changes in Panc1 cells following each treatment, using fluorescence microscopy, n = 3. Images were captured at 100x magnification (scale bar = 100 µm). (b) The proportion of live (green) and dead (red) cells was quantified using ImageJ and normalised to actual cell counts to analyse cell distribution. (c) Diagram of different apoptotic stages: viable cells, early apoptotic cells, late apoptotic cells, and dead/naked nuclei cells. (d) Annexin V-FITC/PI assay was applied to determine the distribution of different stages of apoptotic cells in Panc1 cells using flow cytometry, n = 4. (e) The percentage of each stage of Panc1 cells was statistically quantified by the iQueForecyt software to analyse cell distribution. Data were analysed using GraphPad Prism, with results expressed as mean ± SEM. Comparisons between treatment groups were evaluated using one-way ANOVA to determine statistical significance (*p < 0.05; **p < 0.01; ***p < 0.001, ****p < 0.0001).

    Journal: Frontiers in Pharmacology

    Article Title: Enhancement of gemcitabine toxicity and specificity through PI3K/Akt/Nrf2 pathway inhibition in pancreatic cancer

    doi: 10.3389/fphar.2026.1724989

    Figure Lengend Snippet: Co-administration of gemcitabine and BD B10 induced apoptosis pathway in Panc1 cells. Apoptosis was analysed using multiple methods: (a) AO/PI doubling staining was applied to assess morphological changes in Panc1 cells following each treatment, using fluorescence microscopy, n = 3. Images were captured at 100x magnification (scale bar = 100 µm). (b) The proportion of live (green) and dead (red) cells was quantified using ImageJ and normalised to actual cell counts to analyse cell distribution. (c) Diagram of different apoptotic stages: viable cells, early apoptotic cells, late apoptotic cells, and dead/naked nuclei cells. (d) Annexin V-FITC/PI assay was applied to determine the distribution of different stages of apoptotic cells in Panc1 cells using flow cytometry, n = 4. (e) The percentage of each stage of Panc1 cells was statistically quantified by the iQueForecyt software to analyse cell distribution. Data were analysed using GraphPad Prism, with results expressed as mean ± SEM. Comparisons between treatment groups were evaluated using one-way ANOVA to determine statistical significance (*p < 0.05; **p < 0.01; ***p < 0.001, ****p < 0.0001).

    Article Snippet: Subsequently, the cells were stained with a mixture of Acridine orange and propidium iodide (AO/PI) at 10 μg/mL (AO: 300910250, Thermo Fisher Scientific; PI: P4864, Sigma) in the dark for 5 min at 37 °C.

    Techniques: Staining, Fluorescence, Microscopy, Flow Cytometry, Software