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Nanoscope 5 multimode atomic force microscope

Manufactured by Veeco
Sourced in United States

The Nanoscope V multimode atomic force microscope is a high-performance scanning probe microscope designed for nanoscale imaging and measurement. It utilizes a cantilever-based sensing system to detect and map surface topography with high resolution, providing detailed information about the physical and chemical properties of a wide range of samples.

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4 protocols using nanoscope 5 multimode atomic force microscope

1

Functionalization of Graphene Oxide with PEG

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For GO functionalization, 2 mg of GO was diluted in 2 ml ultrapure DI (Deionized) water and then added 20 mg PEG-NH2. Put those mixtures under sonication for 90 min. Then, the mixture was mixed with 20 mg EDC and stirred for 12 h. Afterward, centrifuged at 20000 rpm for 30 min to remove excess free PEG-NH2. At last, resuspended the precipitate into 2 mL ultrapure DI water. The rGO-PEG was synthesized in the presence of GO-PEG and NaBH4. Last, rGO-PEG with the final concentration of 2 mg/mL was achieved after centrifugation to remove excess free reagents.
The TBK1si/rGO-PEG was diluted with distilled water, put on a copper grid with nitrocellulose, and then stained with phosphotungstic acid. Afterward, it was measured by Nano ZS-90 (Malvern Instruments, Malvern, UK) under room temperature. AFM (atomic force microscopy) images were taken by a Nanoscope V multimode atomic force microscope (Veeco Instruments, USA). TBK1si/rGO-PEG was diluted with ultrapure DI water with a final concentration of 1 × 10−6 M for AFM. Twenty μL TBK1si/rGO-PEG sample was placed on the brand new muscovite mica and dried the samples under critical point dryer. Photos were taken in the tapping mode under room temperature.
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2

Characterization of GO and Fe3O4@SiO2-GO Nanocomposite

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The SEM images were taken with Hitachi- S4160 scanning microscope (Tokyo, Japan) to survey the morphological pattern and surface structural aspects of GO and Fe3O4@SiO2-GO nanocomposite. A Nanoscope V multimode atomic force microscope (Veeco Instruments, USA) were used to perform AFM measurements. The AFM images were taken from samples which prepared by deposition a dispersed GO/methanol solution (70 mg mL−1) onto a mica surface and allowing them to dry in air [25 (link)]. The images were taken under ambient condition by adjusting the instrument on the tapping mode.
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3

Atomic Force Microscopy Analysis of Nanocellulose Suspensions

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Drops of aqueous suspensions (0.2 wt.%) of BNC, VNC, AcBNC, and AcVNC were placed on a mica support and analyzed using a Nanoscope V-Multimode atomic force microscope (Veeco, Santa Barbara, CA, USA) in tapping mode (intermittent contact) using a silicon nitride probe Arrow-NCR-50 (Nano World, Neuchâtel, Switzerland). The resonance frequency of the cantilever was 258 kHz, with a constant force of 42 N m−1 and a tip radius ranging from 5 to 10 nm. Scanning frequencies typically ranged from 1.0 to 1.5 Hz.
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4

Ex Situ AFM Imaging of Amyloid Fibrils

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For ex situ AFM experiments, the appropriate htt-exon1 construct (20 uM) was incubated in the presence or absence of each peptide seed at 37°C and 1400 rpm in an orbital thermomixer for 8 h. After the required incubation time, 5 uL aliquots of each sample were deposited onto freshly cleaved mica (Ted Pella Inc.) for 1 min, washed with 200 uL 18 MΩ·cm ultrapure water, and dried with a stream of filtered air. All samples were imaged using a Nanoscope V MultiMode atomic force microscope (VEECO, Santa Barbara, CA) equipped with a closed loop vertical engage J-scanner and silicon-oxide cantilevers with a resonance frequency of ~300 kHz and nominal spring constant of 40 N/m. All images were analyzed using MATLAB equipped with the image processing toolbox (MathWorks) as described [42 (link)].
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