multimode 5 atomic force microscopy (afm) Search Results


nanoscope iiia multimode 5  (Bruker Corporation)
90
Bruker Corporation nanoscope iiia multimode 5
Nanoscope Iiia Multimode 5, supplied by Bruker Corporation, 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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multimode 5 afm tm afm  (Bruker Corporation)
99
Bruker Corporation multimode 5 afm tm afm
Top-left panel ( a ), high resolution <t>TM-AFM</t> image of a control (colchicine untreated) cell surface. Top-right panel ( b ), histograms presented here are based on counted clusters on the section of cell surface shown in the left panel ( a ). Each histogram represents the number of counted clusters (called frequency, let us assume it as f i , plotted along y-axis. i = 1, 2, 3, …, etc.) versus a height profile (known as particle height, b (top-right panel), let us assume it as h i , plotted in nm scale along x-axis) shown in b. As mentioned in , the height profiles are recorded at the centers of the corresponding clusters (see the left panel), a. Middle and bottom panels present data for cells treated with 1 and 100 µM colchicine, respectively. The higher presence of clusters (in green color) on blue background is visible. We repeated the experiments three times but inspected no substantial changes in the distribution patterns presented in the right panels. Origin 9.1 was used to plot histograms after detecting the numbers using program WSxM. The origin of the detected few events (visible in log plots, see in insets of b) for untreated/control cell surface is nothing but noise.
Multimode 5 Afm Tm Afm, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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multimode 5  (Bruker Corporation)
90
Bruker Corporation multimode 5
Top-left panel ( a ), high resolution <t>TM-AFM</t> image of a control (colchicine untreated) cell surface. Top-right panel ( b ), histograms presented here are based on counted clusters on the section of cell surface shown in the left panel ( a ). Each histogram represents the number of counted clusters (called frequency, let us assume it as f i , plotted along y-axis. i = 1, 2, 3, …, etc.) versus a height profile (known as particle height, b (top-right panel), let us assume it as h i , plotted in nm scale along x-axis) shown in b. As mentioned in , the height profiles are recorded at the centers of the corresponding clusters (see the left panel), a. Middle and bottom panels present data for cells treated with 1 and 100 µM colchicine, respectively. The higher presence of clusters (in green color) on blue background is visible. We repeated the experiments three times but inspected no substantial changes in the distribution patterns presented in the right panels. Origin 9.1 was used to plot histograms after detecting the numbers using program WSxM. The origin of the detected few events (visible in log plots, see in insets of b) for untreated/control cell surface is nothing but noise.
Multimode 5, supplied by Bruker Corporation, 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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multimode 5 - by Bioz Stars, 2026-04
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atomic force microscopy multimode-5  (Veeco)
90
Veeco atomic force microscopy multimode-5
Top-left panel ( a ), high resolution <t>TM-AFM</t> image of a control (colchicine untreated) cell surface. Top-right panel ( b ), histograms presented here are based on counted clusters on the section of cell surface shown in the left panel ( a ). Each histogram represents the number of counted clusters (called frequency, let us assume it as f i , plotted along y-axis. i = 1, 2, 3, …, etc.) versus a height profile (known as particle height, b (top-right panel), let us assume it as h i , plotted in nm scale along x-axis) shown in b. As mentioned in , the height profiles are recorded at the centers of the corresponding clusters (see the left panel), a. Middle and bottom panels present data for cells treated with 1 and 100 µM colchicine, respectively. The higher presence of clusters (in green color) on blue background is visible. We repeated the experiments three times but inspected no substantial changes in the distribution patterns presented in the right panels. Origin 9.1 was used to plot histograms after detecting the numbers using program WSxM. The origin of the detected few events (visible in log plots, see in insets of b) for untreated/control cell surface is nothing but noise.
Atomic Force Microscopy Multimode 5, supplied by Veeco, 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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commercial instrument multimode 5 nanoscope 7.3  (Veeco)
90
Veeco commercial instrument multimode 5 nanoscope 7.3
Top-left panel ( a ), high resolution <t>TM-AFM</t> image of a control (colchicine untreated) cell surface. Top-right panel ( b ), histograms presented here are based on counted clusters on the section of cell surface shown in the left panel ( a ). Each histogram represents the number of counted clusters (called frequency, let us assume it as f i , plotted along y-axis. i = 1, 2, 3, …, etc.) versus a height profile (known as particle height, b (top-right panel), let us assume it as h i , plotted in nm scale along x-axis) shown in b. As mentioned in , the height profiles are recorded at the centers of the corresponding clusters (see the left panel), a. Middle and bottom panels present data for cells treated with 1 and 100 µM colchicine, respectively. The higher presence of clusters (in green color) on blue background is visible. We repeated the experiments three times but inspected no substantial changes in the distribution patterns presented in the right panels. Origin 9.1 was used to plot histograms after detecting the numbers using program WSxM. The origin of the detected few events (visible in log plots, see in insets of b) for untreated/control cell surface is nothing but noise.
Commercial Instrument Multimode 5 Nanoscope 7.3, supplied by Veeco, 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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multimode 5 scanning probe microscope  (Bruker Corporation)
90
Bruker Corporation multimode 5 scanning probe microscope
Top-left panel ( a ), high resolution <t>TM-AFM</t> image of a control (colchicine untreated) cell surface. Top-right panel ( b ), histograms presented here are based on counted clusters on the section of cell surface shown in the left panel ( a ). Each histogram represents the number of counted clusters (called frequency, let us assume it as f i , plotted along y-axis. i = 1, 2, 3, …, etc.) versus a height profile (known as particle height, b (top-right panel), let us assume it as h i , plotted in nm scale along x-axis) shown in b. As mentioned in , the height profiles are recorded at the centers of the corresponding clusters (see the left panel), a. Middle and bottom panels present data for cells treated with 1 and 100 µM colchicine, respectively. The higher presence of clusters (in green color) on blue background is visible. We repeated the experiments three times but inspected no substantial changes in the distribution patterns presented in the right panels. Origin 9.1 was used to plot histograms after detecting the numbers using program WSxM. The origin of the detected few events (visible in log plots, see in insets of b) for untreated/control cell surface is nothing but noise.
Multimode 5 Scanning Probe Microscope, supplied by Bruker Corporation, 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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multimode 5 system  (Veeco)
90
Veeco multimode 5 system
Top-left panel ( a ), high resolution <t>TM-AFM</t> image of a control (colchicine untreated) cell surface. Top-right panel ( b ), histograms presented here are based on counted clusters on the section of cell surface shown in the left panel ( a ). Each histogram represents the number of counted clusters (called frequency, let us assume it as f i , plotted along y-axis. i = 1, 2, 3, …, etc.) versus a height profile (known as particle height, b (top-right panel), let us assume it as h i , plotted in nm scale along x-axis) shown in b. As mentioned in , the height profiles are recorded at the centers of the corresponding clusters (see the left panel), a. Middle and bottom panels present data for cells treated with 1 and 100 µM colchicine, respectively. The higher presence of clusters (in green color) on blue background is visible. We repeated the experiments three times but inspected no substantial changes in the distribution patterns presented in the right panels. Origin 9.1 was used to plot histograms after detecting the numbers using program WSxM. The origin of the detected few events (visible in log plots, see in insets of b) for untreated/control cell surface is nothing but noise.
Multimode 5 System, supplied by Veeco, 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/result/multimode 5 system/product/Veeco
Average 90 stars, based on 1 article reviews
multimode 5 system - by Bioz Stars, 2026-04
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atomic force microscope afm  (Bruker Corporation)
90
Bruker Corporation atomic force microscope afm
Top-left panel ( a ), high resolution <t>TM-AFM</t> image of a control (colchicine untreated) cell surface. Top-right panel ( b ), histograms presented here are based on counted clusters on the section of cell surface shown in the left panel ( a ). Each histogram represents the number of counted clusters (called frequency, let us assume it as f i , plotted along y-axis. i = 1, 2, 3, …, etc.) versus a height profile (known as particle height, b (top-right panel), let us assume it as h i , plotted in nm scale along x-axis) shown in b. As mentioned in , the height profiles are recorded at the centers of the corresponding clusters (see the left panel), a. Middle and bottom panels present data for cells treated with 1 and 100 µM colchicine, respectively. The higher presence of clusters (in green color) on blue background is visible. We repeated the experiments three times but inspected no substantial changes in the distribution patterns presented in the right panels. Origin 9.1 was used to plot histograms after detecting the numbers using program WSxM. The origin of the detected few events (visible in log plots, see in insets of b) for untreated/control cell surface is nothing but noise.
Atomic Force Microscope Afm, supplied by Bruker Corporation, 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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bruker otespa-r3 cantilevers  (Bruker Corporation)
90
Bruker Corporation bruker otespa-r3 cantilevers
Top-left panel ( a ), high resolution <t>TM-AFM</t> image of a control (colchicine untreated) cell surface. Top-right panel ( b ), histograms presented here are based on counted clusters on the section of cell surface shown in the left panel ( a ). Each histogram represents the number of counted clusters (called frequency, let us assume it as f i , plotted along y-axis. i = 1, 2, 3, …, etc.) versus a height profile (known as particle height, b (top-right panel), let us assume it as h i , plotted in nm scale along x-axis) shown in b. As mentioned in , the height profiles are recorded at the centers of the corresponding clusters (see the left panel), a. Middle and bottom panels present data for cells treated with 1 and 100 µM colchicine, respectively. The higher presence of clusters (in green color) on blue background is visible. We repeated the experiments three times but inspected no substantial changes in the distribution patterns presented in the right panels. Origin 9.1 was used to plot histograms after detecting the numbers using program WSxM. The origin of the detected few events (visible in log plots, see in insets of b) for untreated/control cell surface is nothing but noise.
Bruker Otespa R3 Cantilevers, supplied by Bruker Corporation, 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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atomic force microscope  (Bruker Corporation)
90
Bruker Corporation atomic force microscope
Top-left panel ( a ), high resolution <t>TM-AFM</t> image of a control (colchicine untreated) cell surface. Top-right panel ( b ), histograms presented here are based on counted clusters on the section of cell surface shown in the left panel ( a ). Each histogram represents the number of counted clusters (called frequency, let us assume it as f i , plotted along y-axis. i = 1, 2, 3, …, etc.) versus a height profile (known as particle height, b (top-right panel), let us assume it as h i , plotted in nm scale along x-axis) shown in b. As mentioned in , the height profiles are recorded at the centers of the corresponding clusters (see the left panel), a. Middle and bottom panels present data for cells treated with 1 and 100 µM colchicine, respectively. The higher presence of clusters (in green color) on blue background is visible. We repeated the experiments three times but inspected no substantial changes in the distribution patterns presented in the right panels. Origin 9.1 was used to plot histograms after detecting the numbers using program WSxM. The origin of the detected few events (visible in log plots, see in insets of b) for untreated/control cell surface is nothing but noise.
Atomic Force Microscope, supplied by Bruker Corporation, 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/result/atomic force microscope/product/Bruker Corporation
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atomic force microscope - by Bioz Stars, 2026-04
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atomic force microscopy dimension icon multimode 5  (Bruker Corporation)
90
Bruker Corporation atomic force microscopy dimension icon multimode 5
Top-left panel ( a ), high resolution <t>TM-AFM</t> image of a control (colchicine untreated) cell surface. Top-right panel ( b ), histograms presented here are based on counted clusters on the section of cell surface shown in the left panel ( a ). Each histogram represents the number of counted clusters (called frequency, let us assume it as f i , plotted along y-axis. i = 1, 2, 3, …, etc.) versus a height profile (known as particle height, b (top-right panel), let us assume it as h i , plotted in nm scale along x-axis) shown in b. As mentioned in , the height profiles are recorded at the centers of the corresponding clusters (see the left panel), a. Middle and bottom panels present data for cells treated with 1 and 100 µM colchicine, respectively. The higher presence of clusters (in green color) on blue background is visible. We repeated the experiments three times but inspected no substantial changes in the distribution patterns presented in the right panels. Origin 9.1 was used to plot histograms after detecting the numbers using program WSxM. The origin of the detected few events (visible in log plots, see in insets of b) for untreated/control cell surface is nothing but noise.
Atomic Force Microscopy Dimension Icon Multimode 5, supplied by Bruker Corporation, 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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multimode 5 microscope  (Veeco)
90
Veeco multimode 5 microscope
Top-left panel ( a ), high resolution <t>TM-AFM</t> image of a control (colchicine untreated) cell surface. Top-right panel ( b ), histograms presented here are based on counted clusters on the section of cell surface shown in the left panel ( a ). Each histogram represents the number of counted clusters (called frequency, let us assume it as f i , plotted along y-axis. i = 1, 2, 3, …, etc.) versus a height profile (known as particle height, b (top-right panel), let us assume it as h i , plotted in nm scale along x-axis) shown in b. As mentioned in , the height profiles are recorded at the centers of the corresponding clusters (see the left panel), a. Middle and bottom panels present data for cells treated with 1 and 100 µM colchicine, respectively. The higher presence of clusters (in green color) on blue background is visible. We repeated the experiments three times but inspected no substantial changes in the distribution patterns presented in the right panels. Origin 9.1 was used to plot histograms after detecting the numbers using program WSxM. The origin of the detected few events (visible in log plots, see in insets of b) for untreated/control cell surface is nothing but noise.
Multimode 5 Microscope, supplied by Veeco, 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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Image Search Results


Top-left panel ( a ), high resolution TM-AFM image of a control (colchicine untreated) cell surface. Top-right panel ( b ), histograms presented here are based on counted clusters on the section of cell surface shown in the left panel ( a ). Each histogram represents the number of counted clusters (called frequency, let us assume it as f i , plotted along y-axis. i = 1, 2, 3, …, etc.) versus a height profile (known as particle height, b (top-right panel), let us assume it as h i , plotted in nm scale along x-axis) shown in b. As mentioned in , the height profiles are recorded at the centers of the corresponding clusters (see the left panel), a. Middle and bottom panels present data for cells treated with 1 and 100 µM colchicine, respectively. The higher presence of clusters (in green color) on blue background is visible. We repeated the experiments three times but inspected no substantial changes in the distribution patterns presented in the right panels. Origin 9.1 was used to plot histograms after detecting the numbers using program WSxM. The origin of the detected few events (visible in log plots, see in insets of b) for untreated/control cell surface is nothing but noise.

Journal: Membranes

Article Title: Cell Surface Binding and Lipid Interactions behind Chemotherapy-Drug-Induced Ion Pore Formation in Membranes

doi: 10.3390/membranes11070501

Figure Lengend Snippet: Top-left panel ( a ), high resolution TM-AFM image of a control (colchicine untreated) cell surface. Top-right panel ( b ), histograms presented here are based on counted clusters on the section of cell surface shown in the left panel ( a ). Each histogram represents the number of counted clusters (called frequency, let us assume it as f i , plotted along y-axis. i = 1, 2, 3, …, etc.) versus a height profile (known as particle height, b (top-right panel), let us assume it as h i , plotted in nm scale along x-axis) shown in b. As mentioned in , the height profiles are recorded at the centers of the corresponding clusters (see the left panel), a. Middle and bottom panels present data for cells treated with 1 and 100 µM colchicine, respectively. The higher presence of clusters (in green color) on blue background is visible. We repeated the experiments three times but inspected no substantial changes in the distribution patterns presented in the right panels. Origin 9.1 was used to plot histograms after detecting the numbers using program WSxM. The origin of the detected few events (visible in log plots, see in insets of b) for untreated/control cell surface is nothing but noise.

Article Snippet: Two different AFMs were used: Tapping Mode of Bruker MultiMode 5 AFM (TM-AFM) for investigating the cell surface morphology and QNM Mode of Bruker MutiMode 8 AFM (QNM-AFM) for measuring the adhesion forces (the details on both AFM techniques are provided in the ).

Techniques: