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Biochrom
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Thermo Fisher
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Thermo Fisher
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U.S Everbright
deadtm viability cytotoxicity assay kit ![]() Deadtm Viability Cytotoxicity Assay Kit, supplied by U.S Everbright, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/live+deadtm+viability+cytotoxicity+kit/pm34447312-43-2-9 Average 86 stars, based on 1 article reviews
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Thermo Fisher
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Thermo Fisher
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Thermo Fisher
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Everbright USA Inc
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Dojindo Labs
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Image Search Results
Journal: Frontiers in pharmacology
Article Title: Swainsonine Triggers Paraptosis via ER Stress and MAPK Signaling Pathway in Rat Primary Renal Tubular Epithelial Cells.
doi: 10.3389/fphar.2021.715285
Figure Lengend Snippet: FIGURE 2 | SW induced cytoplasmic vacuolization and inhibited cell viability in RTECs (A,B) Phase-contrast images of RTECs following incubation with SW at the indicated concentrations for 24 h. Morphometric analysis of vacuoles was performed with three different areas and the percentage of SW-induced vacuolated cells was calculated (C,D) RTECs were treated with the indicated concentrations of SW for 24 h and cellular viability was measured using Live and DeadTM Viability/Cytotoxicity Assay Kit. Analyze the number of living (green spots) and dead cells (red spots) in three different areas of control and SW-treated cells and the ratios were calculated.
Article Snippet: Live and
Techniques: Incubation, Cytotoxicity Assay, Control
Journal: Frontiers in pharmacology
Article Title: Swainsonine Triggers Paraptosis via ER Stress and MAPK Signaling Pathway in Rat Primary Renal Tubular Epithelial Cells.
doi: 10.3389/fphar.2021.715285
Figure Lengend Snippet: FIGURE 8 | Effects of 4-PBA on SW-induced cytoplasmic vacuolization and cell death. RTECs were pretreated with 4-PBA at the indicated concentrations for 4 h and further treated with 400 μg/ml SW for 24 h (A,B) Western blotting was used to analyze the Bip protein level changes in the presence of 4-PBA. Three independent experiments were performed. *p < 0.05, **p < 0.01 (C,D) Inverted microscopic images of RTECs treated with SW (400 μg/ml) in the presence of 4-PBA. Morphometric analysis of vacuoles was performed with three different areas and the percentage of SW-induced vacuolated cells was calculated (E,F) Cellular viability was assessed using Live and DeadTM Viability/Cytotoxicity Assay Kit. Analyze the number of living (green spots) and dead cells (red spots) in three different areas of control and SW-treated cells and the ratios were calculated.
Article Snippet: Live and
Techniques: Western Blot, Cytotoxicity Assay, Control