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Jem 2100f transmission

Manufactured by JEOL
Sourced in Japan, United States

The JEM-2100F is a transmission electron microscope (TEM) manufactured by JEOL. It is designed to provide high-resolution imaging capabilities for a wide range of research and analytical applications. The JEM-2100F features a field emission gun (FEG) electron source, which enables the production of a high-intensity electron beam for improved image quality and resolution. The microscope is equipped with advanced optics and a user-friendly interface to facilitate efficient operation and data acquisition.

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16 protocols using jem 2100f transmission

1

Characterization of Hierarchical Colloidal Structures

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The properties of HCSs were analyzed using the LabRAM HR 800 Raman spectrometer (HORIBA Scientific, Japan) and characterized using the Nicolet 6700 FT-IR spectrometer (Thermo Electron Corporation, PA, USA). The surface morphology and structure of the samples were observed using the Nova NanoSEM 230 scanning electron microscopy (SEM; FEI, OR, USA) and the JEM-2100F transmission electron microscopy (TEM; JEOL USA Inc., MA, USA).
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2

Multimodal Microscopic Analysis Techniques

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Transmission electron microscopy (TEM) images were taken by a JEOL JEM-2100F transmission electron microscope. Atomic force microscopy (AFM) images were recorded by a Dimension 3100 AFM (Veeco, Fremont, CA, USA) in tapping mode. Fluorescence measurements were performed on a Shimadzu RF-5301 PC fluorophotometer.
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3

Characterization of Au Nanorods

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10 μL of the nanorod solution was applied to 400-mesh copper formvar/carbon grid (Electron Microscope Sciences, Hatfield, PA, USA), and then allowed to dry in air. Afterwards, Au nanorod samples were characterized using 200 kV JEOL JEM-2100F Transmission electron microscope (USA).
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4

Nanovesicle Characterization and Drug Release

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The morphology of nanovesicle was characterized by JEM-2100 F transmission electron microscope (TEM, JEOL, Tokyo, Japan). The mean diameter and zeta potential of the as-prepared nanovesicle was measured by the dynamic laser light scattering (DLS, ZEN 3600, Malvern Instruments). The release profile of 5-FU and NLG919 were tested by high performance liquid chromatography (Waters, USA). 1 H NMR spectra were characterized with a Nuclear Magnetic Resonance instrument (JEOL ECS 400 M).
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5

Cryogenic TEM Imaging of OMMT in Films

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The films were cut into strips (1 mm × 2 mm), and then, they were embedded in a paraffin block and ultramicrotomed under cryogenic conditions (−50 °C) with a thickness of ~100 nm. The selected sections were deposited on a 300 mesh copper grid with a carbon coating. The distribution of OMMT within the film matrix was observed in a bright field imaging mode by JEM-2100F transmission electron microscope (JEOL, Tokyo, Japan). The acceleration voltage was 220 kV, and the magnification was 50,000×.
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6

Characterization of Silver-Loaded Mesoporous Silica Nanoparticles

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Transmission electron microscopic images were measured through JEM-2100F transmission electron microscope (JEOL, Ltd., Japan) under 200 kV accelerating voltage. Energy dispersive X-ray spectroscopy (EDX) was also performed using a JEM-2100F EDX instrument. The morphology of the Ag-MSNs and the bacteria were inspected using a scanning electron microscope (FESEM, S4800, Hitachi Co. Ltd., Tokyo, Japan). The mesoporous properties were determined by the Brunauer-Emmett-Teller (BET) method through Micromeritics ASAP2010 surface area analyzer. The pore diameter was measured from the adsorption branch of the isotherm by the BJH method. X-ray powder diffraction (XRD) investigation was carried out on a Rigaku X-ray diffractometer using Cu Kα radiation. The size distribution and zeta potential were measured by Zetasizer (Nano ZS; Malvern Instruments, Malvern, UK). The silver content of the Ag-MSNs was measured via inductively coupled plasma mass spectrometer (ICP-MS) (Xseries II; Thermo Scientific, Waltham, MA, USA).
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7

Characterization of GBTPs Nanostructures

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GBTPs suspension was diluted to 2 mM, and then 5 μL of the sample was added dropwise to the copper grid. The excess liquid was aspirated with filter paper (Situofan Biotechnology Co., Ltd., Hangzhou, China) after 30 s. Subsequently, 5 μL of the 1% uranyl acetate (Guangdong Fangxin Biotechnology Co., Ltd., Shantou, China) was placed on the grid and removed after 30 s. The sample was observed at 100 kV on a JEM-2100F transmission electron microscope (TEM, JEOL, Japan). A UV spectrophotometer (Genesys 10S, Thermo, USA) was used to measure the UV spectra of GA, BR, TA, and GBTPs solutions, with the scanning wavelength range of 200–600 nm.
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8

Transmission Electron Microscopy Sample Preparation

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JEM-2100F transmission electron microscope (Jeol Ltd, Japan) with 200 kV was used to take the TEM images. The sample grid was prepared by dropping bead solution onto a carbon film coated copper grid (Ted Pella, Inc).
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9

Proteopoylmersome Visualization Protocol

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Solution samples containing proteopolymersome were introduced onto the carbon grid. Subsequently, the solution on the grid was incubated for 5 min; excess solution was then drained off the bottom of the carbon grid using a filter paper. The sample was washed with deionized water and stained by adding an aqueous solution containing 1% of phosphotungstic acid. Excess solution was again drained from the bottom of the carbon grid using a filter paper. Imaging was conducted using a 200-kV JEM-2100F transmission electron microscope (JEOL, Peabody, Massachusetts, USA).
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10

Visualizing Dye Molecule Aggregates

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JEM 2100F Transmission electron microscopy (JEOL company, Japan) were used to photograph the topography of dye molecules at 80 kV. In order to the observation of reactive Orange 13 dye aggregates, a drop of sample solution of Orange 13 dye was placed on 400-mesh formvar copper grids coated with carbon. After the water and solvent evaporate for about 5 minutes, and then observed the surface morphology.
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