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Asylum mfp 3d sa afm

Manufactured by Oxford Instruments
Sourced in United States

The Asylum MFP-3D-SA AFM is an atomic force microscope (AFM) designed for high-resolution imaging and nanoscale measurements. It is capable of operating in various imaging modes and provides accurate topographical data of sample surfaces.

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5 protocols using asylum mfp 3d sa afm

1

Functionalization of AFM Tips for Cell Binding

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The silicon nitride AFM tips (BL-TR400PB-35, Asylum Research, CA) were amino-functionalized with 3-aminopropyl triethoxysilane (APTES) in the gas phase according to the manufacturer’s instructions33 (link) The DBCO-PEG4-NHS (1 mg) in chloroform (0.5 mL) was transferred into the reaction chamber with TEA (30 μL) for 2 h13 (link). The tips were washed with chloroform and dried with nitrogen gas. Then, 500 μL of DV1-N3 solution (394 μM) in PBS was added into the chamber for 2 h. After washing in PBS, the DV1-modified AFM tip was installed on the Asylum MFP-3D SA AFM (Asylum Research, CA) to detect the affinity between the tip and cells. The spring constant of the tips was calibrated every time by the thermal method, where all tips used have a spring constant between 0.02 and 0.04 N m−1. Cells were cultured in a 35 mm Petri dish with 60% confluence. AFM was performed in contact mode, with a trigger voltage of 0.5 V. The scan rate was 1 Hz, and the scan size was 10 μM by 10 μM.
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2

Probing Lipoproteins using Atomic Force Microscopy

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The experiments were performed using an Asylum MFP-3D-SA AFM (Asylum Research, USA) equipped with a scanner of 90 μm × 90 μm × 15 μm in tapping mode for imaging or in contact mode for force measurement. The data were acquired using silicon nitride tips (AppNano, USA) with an end radius of 10 nm and a spring constant of ∼0.04 N/m. After AFM force measurement (obtaining force-vs-distance curves), the Young’s modulus and adhesive force data were directly extracted by the instrument-equipped software (Igor Pro 6.31). To obtain the Young’s modulus, the retrace curve is fitted automatically by the software using the Hertz model. Prior to AFM detection of lipoproteins, the imaging and force measurement of the surfaces of the bare mica and GD-APTES-mica have been performed in air and liquid (data not shown) to exclude the possibility that the detected particles are not lipoproteins.
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3

Quantitative Analysis of Nanoparticle Dimensions

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An Asylum MFP-3D-SA AFM (Asylum Research, USA) equipped with a scanner of 90 μm × 90 μm × 15 μm was utilized. AFM was performed in liquid (PBS) in tapping mode. The data were acquired using silicon nitride tips (AppNano, USA) with an end radius of 10 nm and a spring constant of ~ 0.04 N/m. To obtain topographical images, the AFM probe was scanned across the mica surface (at 0.5–1 Hz) with a tracking force of 300–500 pN. The data were processed using the instrument-equipped software (Igor Pro 6.31) and all images were flattened by one level. Using AFM topographical images, the height (h) and radius (r is half of the full width at half maximum (FWHM)) were measured/calculated. Then, the volume (V) of a single particle was calculated using Eq. 1 [19 (link)], based on which the equivalent diameter of a sphere was calculated. V=π·h/6·3r2+h2
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4

Atomic Force Microscopy of RJEV Vesicles

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RJEV shapes were confirmed using AFM, as previously described.58 (link) Briefly, freshly cleaved mica discs (12-mm diameter; Electron Microscopy Sciences, US) were coated with 50 μL of a 0.1 M solution of poly-L-lysine (PLL) for 5 min. Subsequently, discs were washed three times with double-distilled H2O (ddH2O) and dried with a gentle stream of N2. RJEVs were then immobilized onto the PLL-coated mica by incubation for 30 min at room temperature. Samples were covered to avoid drying and potential dust contamination. After incubation, specimens were washed three times with ddH2O and mounted onto an Asylum MFP 3D-SA AFM (Asylum Research, US). Samples were analyzed in intermittent contact mode (alternating current [AC] mode) with TAP300GD-G cantilevers (BudgetSensors, Bulgaria), obtaining height, amplitude, and phase channel images of substrates under environmental conditions. From the resulting height images, the surface profiles, maximum and mean vesicle height, and RMS roughness of RJEVs were calculated in the Gwyddion 2.56 software. RJEVs from three independent sample preparations were utilized for all AFM-based experiments.
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5

Nanomechanical Analysis of Extracellular Vesicles

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For all AFM imaging, an Asylum MFP 3D-SA AFM (Asylum Research, US) was utilized in intermittent contact mode (AC mode) with TAP300GD-G cantilevers (BudgetSensors, Bulgaria), obtaining height, amplitude, and phase channel images of substrates in air. For HEc-EV nanomechanical analysis, individually calibrated MNSL-10 cantilevers (0.1N/m, Bruker, US) were employed to obtain force-distance curves on the surface of selected EVs in buffer, with a soft loading force of 0.5nN and a 2µm/s rate. HEc-EVs from three independent sample preparations were utilized for all AFM-based experiments.
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