tomographic holographic 3d microscopy Search Results


tomographic holographic 3d microscopy  (NanoLive Inc)
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NanoLive Inc tomographic holographic 3d microscopy
Tomographic Holographic 3d Microscopy, supplied by NanoLive 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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live cell tomographic holographic 3d microscope nanolive 3d cell explorer  (NanoLive Inc)
90
NanoLive Inc live cell tomographic holographic 3d microscope nanolive 3d cell explorer
Effect of BA6 on the viability of various cancer cells and the induction of apoptosis in A549 cells. BA6 reduced the viability of various cancer cells. A549 cells (a), GBM cells (b), U87 cells (c), HepG2 cells (d), HGF cells (e), and OMF cells (f) were treated with the 0, 0.01, 0.1, 1, and 10 μ M concentrations of BA6 for 24 h, respectively, and then, an MTT assay was performed to measure cell viability. Cell viability (%) was expressed as a percentage, as compared to the untreated cells (0 μ M). The results are expressed as the mean ± SEM of three independent experiments. The apoptosis assay of BA6-treated A549 cells was detected by annexin V-FITC (green fluorescence)/propidium iodide (red fluorescence) staining flow cytometry and immunofluorescence TUNEL (green fluorescence) staining. (g) A549 cells treated without and with BA6 (10 μ M) for 24 h are shown with representative four quadrant dot plots from FITC-conjugated annexin V and PI staining. (h) The percentages of early apoptosis (lower right quadrant) and late apoptosis (upper right quadrant) from flow cytometric analysis for A549 cells treated with BA6 for 24 h were assessed. The apoptotic A549 cells were increased, along with increasing concentrations of BA6. Total cells are 20,000 events, and values are the mean ± SEM of three independent experiments. (i) Immunofluorescence showed apoptotic A549 cells marked by the TUNEL assay without or with BA6 (10 μ M) treatment for 24 h. The cell DNA/nuclei were stained using DAPI (blue color) and visualized under a laser confocal <t>microscope</t> (400x). (j) Living cell <t>tomographic</t> microscopy images of A549 cells untreated or treated with BA6 (10 μ M). The significance was determined by Student's t -test: ∗ p < 0.05 and ∗∗ p < 0.01, as compared with the control group.
Live Cell Tomographic Holographic 3d Microscope Nanolive 3d Cell Explorer, supplied by NanoLive 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/product/tomographic+holographic+3d+microscopy/3d+cell+explorer+microscope+nanolive+3d/pmc06530211-63-49-55
Average 90 stars, based on 1 article reviews
live cell tomographic holographic 3d microscope nanolive 3d cell explorer - by Bioz Stars, 2026-11
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holographic tomography 3d explorer  (NanoLive Inc)
90
NanoLive Inc holographic tomography 3d explorer
Effect of BA6 on the viability of various cancer cells and the induction of apoptosis in A549 cells. BA6 reduced the viability of various cancer cells. A549 cells (a), GBM cells (b), U87 cells (c), HepG2 cells (d), HGF cells (e), and OMF cells (f) were treated with the 0, 0.01, 0.1, 1, and 10 μ M concentrations of BA6 for 24 h, respectively, and then, an MTT assay was performed to measure cell viability. Cell viability (%) was expressed as a percentage, as compared to the untreated cells (0 μ M). The results are expressed as the mean ± SEM of three independent experiments. The apoptosis assay of BA6-treated A549 cells was detected by annexin V-FITC (green fluorescence)/propidium iodide (red fluorescence) staining flow cytometry and immunofluorescence TUNEL (green fluorescence) staining. (g) A549 cells treated without and with BA6 (10 μ M) for 24 h are shown with representative four quadrant dot plots from FITC-conjugated annexin V and PI staining. (h) The percentages of early apoptosis (lower right quadrant) and late apoptosis (upper right quadrant) from flow cytometric analysis for A549 cells treated with BA6 for 24 h were assessed. The apoptotic A549 cells were increased, along with increasing concentrations of BA6. Total cells are 20,000 events, and values are the mean ± SEM of three independent experiments. (i) Immunofluorescence showed apoptotic A549 cells marked by the TUNEL assay without or with BA6 (10 μ M) treatment for 24 h. The cell DNA/nuclei were stained using DAPI (blue color) and visualized under a laser confocal <t>microscope</t> (400x). (j) Living cell <t>tomographic</t> microscopy images of A549 cells untreated or treated with BA6 (10 μ M). The significance was determined by Student's t -test: ∗ p < 0.05 and ∗∗ p < 0.01, as compared with the control group.
Holographic Tomography 3d Explorer, supplied by NanoLive 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/product/tomographic+holographic+3d+microscopy/holographic+tomography+3d+explorer/pm38277157-237-26-30
Average 90 stars, based on 1 article reviews
holographic tomography 3d explorer - by Bioz Stars, 2026-11
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live cell tomographic holographic 3d microscope  (NanoLive Inc)
90
NanoLive Inc live cell tomographic holographic 3d microscope
Effect of BA6 on the viability of various cancer cells and the induction of apoptosis in A549 cells. BA6 reduced the viability of various cancer cells. A549 cells (a), GBM cells (b), U87 cells (c), HepG2 cells (d), HGF cells (e), and OMF cells (f) were treated with the 0, 0.01, 0.1, 1, and 10 μ M concentrations of BA6 for 24 h, respectively, and then, an MTT assay was performed to measure cell viability. Cell viability (%) was expressed as a percentage, as compared to the untreated cells (0 μ M). The results are expressed as the mean ± SEM of three independent experiments. The apoptosis assay of BA6-treated A549 cells was detected by annexin V-FITC (green fluorescence)/propidium iodide (red fluorescence) staining flow cytometry and immunofluorescence TUNEL (green fluorescence) staining. (g) A549 cells treated without and with BA6 (10 μ M) for 24 h are shown with representative four quadrant dot plots from FITC-conjugated annexin V and PI staining. (h) The percentages of early apoptosis (lower right quadrant) and late apoptosis (upper right quadrant) from flow cytometric analysis for A549 cells treated with BA6 for 24 h were assessed. The apoptotic A549 cells were increased, along with increasing concentrations of BA6. Total cells are 20,000 events, and values are the mean ± SEM of three independent experiments. (i) Immunofluorescence showed apoptotic A549 cells marked by the TUNEL assay without or with BA6 (10 μ M) treatment for 24 h. The cell DNA/nuclei were stained using DAPI (blue color) and visualized under a laser confocal <t>microscope</t> (400x). (j) Living cell <t>tomographic</t> microscopy images of A549 cells untreated or treated with BA6 (10 μ M). The significance was determined by Student's t -test: ∗ p < 0.05 and ∗∗ p < 0.01, as compared with the control group.
Live Cell Tomographic Holographic 3d Microscope, supplied by NanoLive 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/product/tomographic+holographic+3d+microscopy/live+cell+three+dimensional+holotomographic+microscopy+3d+cell+explorer/pm37375757-496-12-17
Average 90 stars, based on 1 article reviews
live cell tomographic holographic 3d microscope - by Bioz Stars, 2026-11
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cell tomography holographic 3d microscope  (NanoLive Inc)
90
NanoLive Inc cell tomography holographic 3d microscope
Effect of BA6 on the viability of various cancer cells and the induction of apoptosis in A549 cells. BA6 reduced the viability of various cancer cells. A549 cells (a), GBM cells (b), U87 cells (c), HepG2 cells (d), HGF cells (e), and OMF cells (f) were treated with the 0, 0.01, 0.1, 1, and 10 μ M concentrations of BA6 for 24 h, respectively, and then, an MTT assay was performed to measure cell viability. Cell viability (%) was expressed as a percentage, as compared to the untreated cells (0 μ M). The results are expressed as the mean ± SEM of three independent experiments. The apoptosis assay of BA6-treated A549 cells was detected by annexin V-FITC (green fluorescence)/propidium iodide (red fluorescence) staining flow cytometry and immunofluorescence TUNEL (green fluorescence) staining. (g) A549 cells treated without and with BA6 (10 μ M) for 24 h are shown with representative four quadrant dot plots from FITC-conjugated annexin V and PI staining. (h) The percentages of early apoptosis (lower right quadrant) and late apoptosis (upper right quadrant) from flow cytometric analysis for A549 cells treated with BA6 for 24 h were assessed. The apoptotic A549 cells were increased, along with increasing concentrations of BA6. Total cells are 20,000 events, and values are the mean ± SEM of three independent experiments. (i) Immunofluorescence showed apoptotic A549 cells marked by the TUNEL assay without or with BA6 (10 μ M) treatment for 24 h. The cell DNA/nuclei were stained using DAPI (blue color) and visualized under a laser confocal <t>microscope</t> (400x). (j) Living cell <t>tomographic</t> microscopy images of A549 cells untreated or treated with BA6 (10 μ M). The significance was determined by Student's t -test: ∗ p < 0.05 and ∗∗ p < 0.01, as compared with the control group.
Cell Tomography Holographic 3d Microscope, supplied by NanoLive 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/product/tomographic+holographic+3d+microscopy/cell+tomography+holographic+3d+microscope/pm39383975-126-2-7
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cell tomography holographic 3d microscope - by Bioz Stars, 2026-11
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holographic tomographic imaging  (TomoCube Inc)
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TomoCube Inc holographic tomographic imaging
Effect of BA6 on the viability of various cancer cells and the induction of apoptosis in A549 cells. BA6 reduced the viability of various cancer cells. A549 cells (a), GBM cells (b), U87 cells (c), HepG2 cells (d), HGF cells (e), and OMF cells (f) were treated with the 0, 0.01, 0.1, 1, and 10 μ M concentrations of BA6 for 24 h, respectively, and then, an MTT assay was performed to measure cell viability. Cell viability (%) was expressed as a percentage, as compared to the untreated cells (0 μ M). The results are expressed as the mean ± SEM of three independent experiments. The apoptosis assay of BA6-treated A549 cells was detected by annexin V-FITC (green fluorescence)/propidium iodide (red fluorescence) staining flow cytometry and immunofluorescence TUNEL (green fluorescence) staining. (g) A549 cells treated without and with BA6 (10 μ M) for 24 h are shown with representative four quadrant dot plots from FITC-conjugated annexin V and PI staining. (h) The percentages of early apoptosis (lower right quadrant) and late apoptosis (upper right quadrant) from flow cytometric analysis for A549 cells treated with BA6 for 24 h were assessed. The apoptotic A549 cells were increased, along with increasing concentrations of BA6. Total cells are 20,000 events, and values are the mean ± SEM of three independent experiments. (i) Immunofluorescence showed apoptotic A549 cells marked by the TUNEL assay without or with BA6 (10 μ M) treatment for 24 h. The cell DNA/nuclei were stained using DAPI (blue color) and visualized under a laser confocal <t>microscope</t> (400x). (j) Living cell <t>tomographic</t> microscopy images of A549 cells untreated or treated with BA6 (10 μ M). The significance was determined by Student's t -test: ∗ p < 0.05 and ∗∗ p < 0.01, as compared with the control group.
Holographic Tomographic Imaging, supplied by TomoCube 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/product/tomographic+holographic+3d+microscopy/holographic+tomographic+imaging/10__1016_slash_j__cej__2024__154142-117-1-9
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holographic tomographic imaging - by Bioz Stars, 2026-11
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Effect of BA6 on the viability of various cancer cells and the induction of apoptosis in A549 cells. BA6 reduced the viability of various cancer cells. A549 cells (a), GBM cells (b), U87 cells (c), HepG2 cells (d), HGF cells (e), and OMF cells (f) were treated with the 0, 0.01, 0.1, 1, and 10 μ M concentrations of BA6 for 24 h, respectively, and then, an MTT assay was performed to measure cell viability. Cell viability (%) was expressed as a percentage, as compared to the untreated cells (0 μ M). The results are expressed as the mean ± SEM of three independent experiments. The apoptosis assay of BA6-treated A549 cells was detected by annexin V-FITC (green fluorescence)/propidium iodide (red fluorescence) staining flow cytometry and immunofluorescence TUNEL (green fluorescence) staining. (g) A549 cells treated without and with BA6 (10 μ M) for 24 h are shown with representative four quadrant dot plots from FITC-conjugated annexin V and PI staining. (h) The percentages of early apoptosis (lower right quadrant) and late apoptosis (upper right quadrant) from flow cytometric analysis for A549 cells treated with BA6 for 24 h were assessed. The apoptotic A549 cells were increased, along with increasing concentrations of BA6. Total cells are 20,000 events, and values are the mean ± SEM of three independent experiments. (i) Immunofluorescence showed apoptotic A549 cells marked by the TUNEL assay without or with BA6 (10 μ M) treatment for 24 h. The cell DNA/nuclei were stained using DAPI (blue color) and visualized under a laser confocal microscope (400x). (j) Living cell tomographic microscopy images of A549 cells untreated or treated with BA6 (10 μ M). The significance was determined by Student's t -test: ∗ p < 0.05 and ∗∗ p < 0.01, as compared with the control group.

Journal: Oxidative Medicine and Cellular Longevity

Article Title: BA6 Induces Apoptosis via Stimulation of Reactive Oxygen Species and Inhibition of Oxidative Phosphorylation in Human Lung Cancer Cells

doi: 10.1155/2019/6342104

Figure Lengend Snippet: Effect of BA6 on the viability of various cancer cells and the induction of apoptosis in A549 cells. BA6 reduced the viability of various cancer cells. A549 cells (a), GBM cells (b), U87 cells (c), HepG2 cells (d), HGF cells (e), and OMF cells (f) were treated with the 0, 0.01, 0.1, 1, and 10 μ M concentrations of BA6 for 24 h, respectively, and then, an MTT assay was performed to measure cell viability. Cell viability (%) was expressed as a percentage, as compared to the untreated cells (0 μ M). The results are expressed as the mean ± SEM of three independent experiments. The apoptosis assay of BA6-treated A549 cells was detected by annexin V-FITC (green fluorescence)/propidium iodide (red fluorescence) staining flow cytometry and immunofluorescence TUNEL (green fluorescence) staining. (g) A549 cells treated without and with BA6 (10 μ M) for 24 h are shown with representative four quadrant dot plots from FITC-conjugated annexin V and PI staining. (h) The percentages of early apoptosis (lower right quadrant) and late apoptosis (upper right quadrant) from flow cytometric analysis for A549 cells treated with BA6 for 24 h were assessed. The apoptotic A549 cells were increased, along with increasing concentrations of BA6. Total cells are 20,000 events, and values are the mean ± SEM of three independent experiments. (i) Immunofluorescence showed apoptotic A549 cells marked by the TUNEL assay without or with BA6 (10 μ M) treatment for 24 h. The cell DNA/nuclei were stained using DAPI (blue color) and visualized under a laser confocal microscope (400x). (j) Living cell tomographic microscopy images of A549 cells untreated or treated with BA6 (10 μ M). The significance was determined by Student's t -test: ∗ p < 0.05 and ∗∗ p < 0.01, as compared with the control group.

Article Snippet: A549 cells were seeded overnight in a glass bottom microwell dish after BA6 treatment with concentrations of 0 (as control) and 10 μ M for 24 h. However, visualization of the 3D live cell morphology of A549 cells and localization of QD were performed by interferometric detection using a live cell tomographic holographic 3D microscope Nanolive (3D Cell Explorer, Lausanne, Switzerland) and processed using STEVE software (3D Cell Explorer).

Techniques: MTT Assay, Apoptosis Assay, Fluorescence, Staining, Flow Cytometry, Immunofluorescence, TUNEL Assay, Microscopy, Control