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Talos f200s tem

Manufactured by Thermo Fisher Scientific
Sourced in United States

The Talos F200S TEM is a transmission electron microscope (TEM) designed and manufactured by Thermo Fisher Scientific. It is capable of high-resolution imaging and analysis of a wide range of materials at the nanometer scale. The Talos F200S TEM provides advanced electron optics and features that enable researchers to obtain detailed structural and compositional information about their samples.

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6 protocols using talos f200s tem

1

Characterization of QD-loaded PSMPs

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The HAADF-STEM measurements of both QD-loaded PSMPs were carried out with a ThermoFisher Scientific Talos F200S TEM at 200 kV. The samples were prepared by drop-casting diluted dispersions of the respective PSMPs in ethanol onto lacey, carbon-coated copper grids (PELCO by Ted Pella, Inc., 400 mesh).
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2

HAADF-STEM Imaging of NP-Stained PSMPs

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For the HAADF-STEM measurements of the NP-stained PSMPs, the samples were drop-casted from diluted PSMP dispersions in ethanol onto carbon-coated copper grids (PELCO by Ted Pella, Inc., 400 mesh). For the NPL-stained PSMPs, lacey grids with otherwise the same specifications were used. Imaging was performed with a ThermoFisher Scientific Talos F200S TEM at 200 kV.
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3

Microstructural Characterization of Synthesized Materials

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The synthesised materials were characterised by Scanning Transmission Electron Microscopy (STEM) and Energy Dispersive X-ray (EDX) analysis to gain information on the microstructural features and elemental distribution. Samples were prepared by mixing a spatula tip of the respective dry powder with 300 μL ethanol (>99.9%, LiChrosolve, Supelco) in an Eppendorf tube. The sample was then sonicated for 2 min and left to sediment for 1 min. A volume of 10 μL from the supernatant was then drawn through a holey carbon nickel grid. After drying, most of the materials were analysed on a Talos F200× STEM (Thermo Fisher Scientific) and TCF-M-5c material by Titan Themis 200 (FEI) STEM equipped with the SuperX EDX system, both operated at an accelerating voltage of 200 kV. High-Angle Annular Dark-Field (HAADF) STEM images were obtained in conjunction with EDX elemental maps. Data was processed using the software Velox (Version 3.0.0.815, Thermo Fisher Scientific).
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4

Phage Particle Visualization via TEM

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Purified phage particles with a titer of 1011 PFU/mL were loaded onto a copper grid for 1 min, followed by negative staining with uranyl acetate (2% w/v) for 1 min and subsequent aspiration of excess liquid. After drying, the Talos™ F200S TEM (Thermo Fisher Scientific, Waltham, MA, USA) apparatus was used to observe the morphology of phages and to capture images.
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5

Transmission Electron Microscopy of AuNCs and Brain Slices

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The TEM measurements of AuNCs were performed by using a Talos F200S TEM (Thermo Fisher, USA) with an accelerating voltage of 200 kV. The TEM images of the brain slices were performed by using a FEI Tecnai G20 TEM (FEI, USA) with an accelerating voltage of 200 kV. Blinded observation of samples with random selection of grid areas was implemented to reduce bias during imaging.
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6

Multi-Technique Characterization of Nanoparticles

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The morphologies of the samples were observed by a Talos F200S TEM (ThermoFisher, Czech Rep). The hydrodynamic diameters and zeta potentials were measured on a Zetasizer Nano ZS 90 unit (Malvern, UK). X‐ray photoelectron spectroscopy (XPS) was performed on a K‐Alpha photoelectron spectrometer (ThermoScientific, UK). FT‐IR spectra were obtained from a Nicolet iS50 FT‐IR spectrometer (ThermoFisher, UK). 1H NMR spectra were recorded on an AVANCE NEO 400 spectrometer (Bruker, Switzerland, DMSO‐d6 as solvent). UV–Vis absorption spectra were measured using a UV‐6100 ultraviolet spectrometer (Metash, China). FL spectra were acquired from a RF‐6000 fluorospectrophotometer (Shimadzu, Japan). The purity of the material was determined by a HPLC‐MS/MS method (Agilent, UK). In vitro and in vivo PA images and data were collected by a VEVO LAZR‐X small animal photoacoustic imaging system (Fujifilm VisualSonics, UK). In vitro and in vivo FL images and data were obtained by an IVIS Lumina III small animal optical imaging system (PerkinElmer, UK). MTS results were acquired from a microplate reader (BioTek, UK). Cell uptake was observed by a CytoFLEX LX flow cytometry (Beckman Coulter, UK). Cell FL images were captured on a TCS SP8 DIVE CLSM (Leica, Germany). Cell staining images were obtained from a IX71 inverted fluorescence microscope (Olympus, Japan).
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