Review



multimode 5 afm tm afm  (Bruker Corporation)


Bioz Verified Symbol Bruker Corporation is a verified supplier  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 99
      Buy from Supplier

    Structured Review

    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 10220 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/multimode+5+afm+tm+afm/pmc08304557-112-9-8
    Average 99 stars, based on 10220 article reviews
    multimode 5 afm tm afm - by Bioz Stars, 2026-09
    99/100 stars

    Images

    1) Product Images from "Cell Surface Binding and Lipid Interactions behind Chemotherapy-Drug-Induced Ion Pore Formation in Membranes"

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

    Journal: Membranes

    doi: 10.3390/membranes11070501

    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.
    Figure Legend 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.

    Techniques Used:

    Related Articles

    other:

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



    Similar Products

    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
    https://www.bioz.com/product/multimode+5+afm+tm+afm/pmc08304557-112-9-8
    Average 99 stars, based on 1 article reviews
    multimode 5 afm tm afm - by Bioz Stars, 2026-09
    99/100 stars
    		  Buy from Supplier

    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: