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flow cytometry analysis with propidium iodide staining  (Becton Dickinson)

 
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    Becton Dickinson flow cytometry analysis with propidium iodide staining
    Flow Cytometry Analysis With Propidium Iodide Staining, supplied by Becton Dickinson, 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/flow+cytometry+analysis+with+propidium+iodide+staining/propidium+iodide++pi++staining+flow+cytometry/pm22360315-45-23-26
    Average 90 stars, based on 1 article reviews
    flow cytometry analysis with propidium iodide staining - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Lysis:

    Article Title: Phenotyping of Staphylococcus aureus reveals a new virulent ST398 lineage.
    Article Snippet: For the lysis test, isolated PMNs (2.5 · 106/mL) were resuspended in SaS/IMDM/5% homologous heat-inactivated serum and incubated for 10 min (37 C). .. The lysis reaction was stopped with ice-cold NaCl (0.9%), and the proportion of dead cells was immediately determined by flow cytometry analysis with propidium iodide staining (Becton Dickinson, San Jose, CA, USA; Lot 38974000). ..

    Flow Cytometry:

    Article Title: Phenotyping of Staphylococcus aureus reveals a new virulent ST398 lineage.
    Article Snippet: For the lysis test, isolated PMNs (2.5 · 106/mL) were resuspended in SaS/IMDM/5% homologous heat-inactivated serum and incubated for 10 min (37 C). .. The lysis reaction was stopped with ice-cold NaCl (0.9%), and the proportion of dead cells was immediately determined by flow cytometry analysis with propidium iodide staining (Becton Dickinson, San Jose, CA, USA; Lot 38974000). ..

    Staining:

    Article Title: Phenotyping of Staphylococcus aureus reveals a new virulent ST398 lineage.
    Article Snippet: For the lysis test, isolated PMNs (2.5 · 106/mL) were resuspended in SaS/IMDM/5% homologous heat-inactivated serum and incubated for 10 min (37 C). .. The lysis reaction was stopped with ice-cold NaCl (0.9%), and the proportion of dead cells was immediately determined by flow cytometry analysis with propidium iodide staining (Becton Dickinson, San Jose, CA, USA; Lot 38974000). ..



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    flow cytometry analysis with propidium iodide staining  (Becton Dickinson)
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    flow cytometry analysis of isolated nuclei stained with propidium iodide  (Becton Dickinson)
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    Susceptibility to apoptosis of U937Bcl-2 and U937pMEP cells. Both transfectants were treated with 𝒟(−)lentiginosine at the concentration of 10, 50, 100, 250, 500 and 1000 μ M for 18 h. The data on Y-axis are expressed as percentage hypodiploid nuclei, as detected by <t>propidium</t> iodide staining and flow cytometry analysis. As a positive control, etoposide at the concentration of 50 μ M was used. Data are presented as mean values±S.D. from three experiments performed in duplicate ( n =6). Asterisks (**) indicate highly significant differences between treated and untreated cells ( P <0.001)
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    Susceptibility to apoptosis of U937Bcl-2 and U937pMEP cells. Both transfectants were treated with 𝒟(−)lentiginosine at the concentration of 10, 50, 100, 250, 500 and 1000 μ M for 18 h. The data on Y-axis are expressed as percentage hypodiploid nuclei, as detected by <t>propidium</t> iodide staining and flow cytometry analysis. As a positive control, etoposide at the concentration of 50 μ M was used. Data are presented as mean values±S.D. from three experiments performed in duplicate ( n =6). Asterisks (**) indicate highly significant differences between treated and untreated cells ( P <0.001)
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    Susceptibility to apoptosis of U937Bcl-2 and U937pMEP cells. Both transfectants were treated with 𝒟(−)lentiginosine at the concentration of 10, 50, 100, 250, 500 and 1000 μ M for 18 h. The data on Y-axis are expressed as percentage hypodiploid nuclei, as detected by propidium iodide staining and flow cytometry analysis. As a positive control, etoposide at the concentration of 50 μ M was used. Data are presented as mean values±S.D. from three experiments performed in duplicate ( n =6). Asterisks (**) indicate highly significant differences between treated and untreated cells ( P <0.001)

    Journal: Cell Death & Disease

    Article Title: 𝒟(−)lentiginosine-induced apoptosis involves the intrinsic pathway and is p53-independent

    doi: 10.1038/cddis.2012.97

    Figure Lengend Snippet: Susceptibility to apoptosis of U937Bcl-2 and U937pMEP cells. Both transfectants were treated with 𝒟(−)lentiginosine at the concentration of 10, 50, 100, 250, 500 and 1000 μ M for 18 h. The data on Y-axis are expressed as percentage hypodiploid nuclei, as detected by propidium iodide staining and flow cytometry analysis. As a positive control, etoposide at the concentration of 50 μ M was used. Data are presented as mean values±S.D. from three experiments performed in duplicate ( n =6). Asterisks (**) indicate highly significant differences between treated and untreated cells ( P <0.001)

    Article Snippet: Apoptosis was assessed through flow cytometry analysis of isolated nuclei stained with propidium iodide, carried out on a Becton Dickinson FACS analyser, or by morphological analysis following staining with Hoechst chromatin dye, as previously described by some of us.,

    Techniques: Concentration Assay, Staining, Flow Cytometry, Positive Control