flow cytometry staining analysis Search Results


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GraphPad Software Inc flow cytometry analysis with annexin v and pi double staining
Flow Cytometry Analysis With Annexin V And Pi Double Staining, supplied by GraphPad Software Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Oxford Nanoimaging Ltd beads with exosomes stained for flow cytometry analysis for cd63 (alexa fluor 647 anti-human cd63)
Beads With Exosomes Stained For Flow Cytometry Analysis For Cd63 (Alexa Fluor 647 Anti Human Cd63), supplied by Oxford Nanoimaging Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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KU Leuven optimized staining protocols for intracellular cytokine analysis by flow cytometry
Optimized Staining Protocols For Intracellular Cytokine Analysis By Flow Cytometry, supplied by KU Leuven, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Blackwell Science Ltd flow cytometry analysis of tunel stained cells
Flow Cytometry Analysis Of Tunel Stained Cells, supplied by Blackwell Science Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Becton Dickinson flow cytometry analysis of isolated nuclei stained with propidium iodide
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)
Flow Cytometry Analysis Of Isolated Nuclei Stained With Propidium Iodide, 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
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Tree Star Inc flow cytometry and intracellular cytokine staining analysis
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)
Flow Cytometry And Intracellular Cytokine Staining Analysis, supplied by Tree Star Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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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