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The atomic force microscope (AFM) has long been recognized as a useful tool for measuring mechanical properties of materials. Until recently though, it has been impossible to achieve truly quantitative material property mapping with the resolution and convenience demanded by AFM researchers. A number of recent AFM mode innovations have taken aim at
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What is the maximum viscosity the tapping mode can perform in? Does scan assist make the imaging easier in high viscosity fluids
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How does PeakForce QNM mode comparing to Tapping mode Phase Imaging and Harmonix mode
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Are there any sample types where you would recommend using standard tapping or contact mode instead of peak force tapping
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In showing the scan asyst versus tapping I don't understand how scan asyst doesn't have the same problem of the material sticking to the tip that it has in tapping mode.
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What are the key parameter differences between TappingMode and ScanAsyst?
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Will tapping mode will not be available for good and be replaced by scan asyst?
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Syndiotactic Polypropylene s-PP: 130 degrees C, 40µm scan Crystallization in 14 hours. Syndiotactic Polypropylene s-PP: 125 degrees C, 40µm scan Crystallization in 3 hours. Syndiotactic Polypropylene s-PP: 120 degrees C, 40µm scan Crystallization in Less than 1 Hours. Syndiotactic Polypropylene s-PP: 120 degrees
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Many of the biological samples suitable for imaging with atomic force microscopy (AFM) are subject to artifacts if they are dried. This problem is not unique to AFM imaging. It has long been a concern in electron microscopy and methods have been developed to minimize its effect with that imaging technique (namely fixation, critical point drying, and
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Atomic force microscopy (AFM) provides the ability to perform three-dimensional measurements of surface structures at nanometer-to-subangstrom resolution in ambient and liquid environments. These capabilities have led to ground-breaking life sciences advances in the investigation of DNA, proteins, and cells.1 In particular, pharmaceutical research involves