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Jem 2010 transmission electron microscope

Manufactured by JEOL
Sourced in Japan, United States

The JEM-2010 is a transmission electron microscope (TEM) manufactured by JEOL. It is designed to provide high-resolution imaging and analysis of samples at the nanoscale level. The JEM-2010 utilizes an electron beam to produce magnified images of the internal structure and composition of various materials.

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33 protocols using jem 2010 transmission electron microscope

1

Characterization of DACNC and Ery-DACNC

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The surface morphology of DACNC and Ery-DACNC was observed using a JEOL JEM-2010 transmission electron microscope (TEM) (JEOL, Tokyo, Japan). VK-9500 3D profile laser microscope (Keyence, Taipei, Taiwan) was used to monitor the appearance of DACNC and Ery-DACNC powders after freeze-drying. The coating was observed using a JEOL JSM-7000 field-emission scanning electron microscope (FE–SEM) (JEOL). The bonding between erythrosine and DACNC was investigated using Nicoleti S5 Fourier transform infrared (FTIR) spectroscopy (Thermo Fisher Scientific, Madison, WI, USA). The surface morphologies of the films were analyzed.
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2

Transmission Electron Microscopy of Bacterial Cells

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Cells of the strain ChlSP were harvested by centrifugation (3,500 rpm and 5 min), fixed with equal parts of fresh 2.5% (v/v) glutaraldehyde and 4% (v/v) purified paraformaldehyde buffered with 0.1 M sodium cacodylate, pH 7, at 4°C overnight, and stained in 2% (v/v) OsO4 for 1 h at 4°C. Pelleted cells were dehydrated in increasing concentrations of acetone and embedded in Spurr resin. Sections of 80 nm thickness (sectioned with an LKB 2088 ultra-microtome) were collected on copper grids (Sigma-Aldrich, Germany) and examined with a JEOL JEM-2010 transmission electron microscope (Jeol Ltd., Tokyo, Japan) operated at 100 kV.
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3

Ultrastructural Analysis of T. marneffei Infection

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Transmission electron microscopy (TEM) was performed to illustrate the intracellular structure of T. marneffei within THP-1 macrophages. Monolayers of differentiated THP-1 cells (1×106 cells/well) in 6 well tissue culture plates were infected with T. marneffei conidia at MOI 10:1 conidia/macrophage ratio. After 36 hours of co-incubation at 37°C with 5% CO2, THP-1 infected with T. marneffei were removed by trypsinization, neutralized by completed RPMI-1640 and washed three times with PBS (27 (link)). Subsequently, intact T. marneffei infected THP-1 cells were fixed with 2.5% glutaraldehyde in 0.1M phosphate buffer and post fixed with 2% osmium tetroxide in PBS for 1 hour. Next, the samples were dehydrated with graded ethyl alcohol series, starting with 50, 70, 85, 95% and three exchanged with anhydrous absolute ethyl alcohol in the final step and then embedded in Epon-812 epoxy resin. The samples were then polymerized in a 60 °C in hot air oven for approximately 72 hours and ultrathin sections were cut at a thickness of 60-90 nm. The processed samples were mounted with uranyl acetate and viewed in a JEOL JEM- 2010 transmission electron microscope (JEOL, Tokyo, Japan), with an accelerating voltage 200 kV.
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4

Comprehensive Characterization of Nanoparticles

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NMR spectra were performed on a Bruker ARX 400 NMR spectrometer. Electrospray ionization mass spectrometry (ESI-MS) was performed on a Proteome X-LTQ. Particle size and size distribution were determined by laser light scattering (LLS) with a particle size analyzer (90 Plus, Brookhaven Instruments Co., United States) at a fixed angle of 90° at room temperature. The zeta potential was determined by a Malvern Zetasizer Nano ZS90 (Worcestershire, UK). TEM images were obtained from a JEOL JEM-2010 transmission electron microscope with an accelerating voltage of 200 KV. UV-vis absorption spectra were taken on a Shimadzu Model UV-1700 spectrometer. Photoluminescence (PL) spectra were measured on a Perkin-Elmer LS 55 spectrofluorometer. All UV and PL spectra were collected at 24 ± 1 °C.
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5

Cryo-TEM Imaging of Liposomes

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Vitreous ice TEM samples of liposomes
were prepared for imaging. First, the TEM grids were ionized by glow
discharging for 1 min with a 5 mA discharge. The next stages of sample
preparation were all performed using a Vitrobot type FP5350/60. The
liposome suspension or nanofiber solution was added to the grid and
immediately blotted for 2 s in a humidity-controlled chamber before
being immersed in liquid ethane. The grid is then manually transferred
from the liquid ethane to liquid nitrogen where it is stored until
imaging. All TEM imaging was performed on a 200 kV JEM 2010 transmission
electron microscope (JEOL USA Inc., Peabody, MA) and cryo-imaging
was taken at a temperature of −176 °C using minimum dose
system (MDS) mode.
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6

Cysteine-Stabilized Fluorescent Iron Oxide Nanoparticles

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All chemicals and reagents used in this work were AR grade 1 unless noticed and purchased from Sigma-Aldrich Chemical Corporation, including HAuCl4, L-cysteine (L-Cys) and anhydrous FeCl3. Other inorganic chemicals were purchased from Tianjin Chemical Corporation. Solvent water was purified and obtained from Millipore. All glassware was first treated with aqua regia at 40°C and then washed with purified water. XPS and DLS experiments were carried out by a PHI-5000 Versaprobe III X-ray photon–electron spectrophotometer (ULVCA-PHI, United States) and a Malvern Zetasizer Nano ZS90 laser particle size and zeta potential analyzer (Trek, Taiwan). IR spectra were recorded using a Bruker Vertex 70 FTIR spectrometer. The TEM image was obtained with a JEM-2010 transmission electron microscope (JEOL, Japan). UV-vis absorption spectra were obtained using a Shimadzu UV-3101PC spectrophotometer and a Biotek ELx800 automatic enzyme-linked immunosorbent assay. Emission spectra were recorded using a Hitachi F-7000 fluorescence spectrophotometer (Xe lamp). Emission quantum yield was determined by using this Hitachi F-7000 fluorescence spectrophotometer with the help of an integrating sphere. The reference was quinine sulfate (20 μM) in diluted H2SO4 (0.1 M). The emission lifetime was measured with a TEKTRONIX TDS-3052 oscilloscope (excited by an optical parametric oscillator).
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7

Transmission Electron Microscopy of MEVs

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JEM-2010 transmission electron microscope (, 80 kV, JEOL, Tokyo, Japan) was employed to examine 0.2 mg/mL MEVs. The samples were fixed in mesh carbon-layered copper grids (400) for 2 min and the surplus preparations were drained using blotting paper. Samples were then stained with 10 µL of 2% (w/v) uranyl acetate solution (Electron Microscopy Services) before imaging.
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8

Physicochemical Characterization of Nanodiamonds

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Nanodiamonds and EPND (0.1–0.2 mg/mL, nanodiamond concentration) were suspended in deionized water within disposable micro cuvettes. Hydrodynamic size and ζ-potential measurements were performed on a Zetasizer Nano (Malvern, UK). Final values were averages of three or more separate measurements of each sample. Fourier transform infrared spectroscopy was performed using a PerkinElmer FTIR spectrum 2000 over a range of 400–4000 cm–1. Samples were dried using a rotary evaporator. Five mg of sample was mixed with 0.1 g of KBr powder using mortar and pestle before pressing the sample to a thin film of which the spectra were taken. Transmission electronic microscopy was performed using a JEOL JEM-2010 transmission electron microscope. The nanodiamond and EPND were sonicated in water at a concentration of 0.5 mg/mL, and the suspension was dropped on the copper grid (coated with carbon film), then dried overnight at room temperature prior to imaging.
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9

Comprehensive Characterization of g-C3N4

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The phase composition of g-C3N4 was identified by XRD, recorded on a Rigaku D/max-3B X-ray diffractometer (Cu-Kα radiation, λ = 0.15418 nm) over the 2θ range of 10°-60° at 40 kV and 30mA. The chemical groups in g-C3N4 structure were confirmed by FT-IR, operated on a Nicolet Nexus infrared spectrometer after mixture of g-C3N4 sample with spectroscopic grade KBr (300 mg). The crystal morphology and microstructure of g-C3N4 were observed by SEM and TEM, realized on FEISirion200 scanning electron microscope and JEOL JEM-2010 transmission electron microscope, respectively. X-ray photoelectron spectroscopy (XPS) with Al Kα X-rays radiation (AXIS ULTRADLD, Kratos) was used to investigate the element compositions and surface properties of the samples. The binding energy was corrected using C1s (284.6 eV) as the internal standard. DRS spectra, recorded in the range of 400–800 nm, were implemented on an USB4000 UV-vis spectrometer (Ocean Optics) equipped with an integral sphere, using a standard template provided by South Africa Optics as the reference. The BET specific surface area of g-C3N4 was measured on a Sibata SA-1100 surface area analyzer, according to the nitrogen adsorption-desorption data at liquid nitrogen temperature. Surface Zeta potentials of g-C3N4 were examined by Zeta potential analyzer (Nano-ZS90) at different pH values.
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10

Transmission Electron Microscopy of Milk EVs

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EV samples (0.2 µg/µL) obtained from all four milk samples were examined in a JEM-2010 transmission electron microscope (JEOL, 80 kV, Akishima, Tokyo) or Tecnai TF30 transmission electron microscope (FEI, 300 kV, Lausanne, Switzerland), as described previously [35 (link)].
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