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Em 912 omega

Manufactured by Zeiss
Sourced in Germany

The EM 912 Omega is a transmission electron microscope (TEM) manufactured by Zeiss. It is designed for high-resolution imaging and analysis of a wide range of materials. The EM 912 Omega utilizes an accelerating voltage of up to 120 kV and features advanced optics and detectors to provide detailed information about the structure and composition of samples at the nanoscale.

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17 protocols using em 912 omega

1

Ultrastructural Analysis of Plant Leaves

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Light microscopy images were obtained with an Olympus Epi-Fluorescence Microscope (BX-51) essentially as described previously (Lu et al., 2017) (link). Samples for TEM were prepared using published procedures (Lu et al., 2017 (link); Armarego-Marriott et al., 2019) (link) with minor modifications. Briefly, leaf samples were fixed in 2.5% (v/v) glutaraldehyde in 50 mM sodium cacodylate (pH 7.4) containing 5 mM CaCl2 for 1 h under vacuum. Fixation was continued at 4°C overnight, and followed by post-fixation with 1% (w/v) OsO4 and 0.8% (w/v) K3Fe(CN)6 in 50 mM cacodylate buffer (pH 7.4) for 2 h at 4°C. After rinsing the leaf samples, en bloc staining of the tissue was performed by incubation in 2% (w/v) aqueous uranyl acetate for 2 h at root temperature. Following dehydration in acetone, embedding in Epon-812 (Science Services GmbH, Munich, Germany) was carried out using standard protocols. For electron microscopy, ultrathin sections (50–70 nm) were cut with diamond knives, contrasted with 2% (w/v) uranyl acetate and lead citrate, and examined in a Zeiss EM 912 Omega transmission electron microscope (Carl Zeiss, Oberkochen, Germany).
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2

Transmission Electron Microscopy of Cotyledons

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Cotyledons from Col-0 and deip1 mutants were fixed in Karnovsky’s solution [2.5% (w/v) glutaraldehyde, 2% (w/v) paraformaldehyde, 0.1 M sodium cacodylate buffer pH 7.4]. The samples were post-fixed with 2% (w/v) osmium tetroxide for 2 h on ice, washed for 15 min with 0.1 M sodium cacodylate buffer pH 7.4, and washed trice with deionized water for 10 min each. The samples were then post-stained with 2% (w/v) uranyl acetate for 2 h at 4 °C, washed for 10 min with miliQ water and dehydrated with increasing concentrations of ethanol [10 min 30% (v/v); 15 min 50%; 30 min 70%, 40 min 80%; 40 min 90% and overnight 100%]. The dehydrated samples were infiltrated with Agar100 epoxy resin (agar scientific) and embedded by incubation at 60 °C for 48 h. Ultrathin sections (50–70 nm) were cut with diamond knives, contrasted with 2% (w/v) uranyl acetate and lead citrate, and examined in a Zeiss EM 912 Omega transmission electron microscope (Carl Zeiss, Oberkochen, Germany)78 (link).
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3

Transmission Electron Microscopy Imaging

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Images were acquired using a Zeiss TEM system (Zeiss EM912 OMEGA) equipped with a camera (TRS Sharp Eye 2k slow-scan CCD, Tröndle, Moorenweis, Moorenweis) and controlled by the Olympus iTEM software (Olympus, Tokyo, Japan).
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4

Transmission Electron Microscopy Analysis

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Transmission electron microscopy (TEM) measurements were performed on a Zeiss EM 912 Omega (Carl Zeiss AG, Germany) transmission electron microscope operated at 300 kV and equipped with an electron-diffraction (ED) unit. High-resolution transmission electron microscopy (HRTEM) was performed by TEM in a Philips CM30 operated at 300
kV. The samples were ultramicrotomed (Leica EM FC6) and placed onto carbon-coated copper grids.
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5

Immunodetection of VGLUT3 in Hippocampus

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VGLUT3 was detected with an electron microscope with a post-embedding immunogold method as previously described (Gras et al., 2002 (link), 2008 (link)). Sagittal brain sections of the hippocampus were incubated with guinea pig anti-VGLUT3 antiserum (1:1000). Immunolabeling was detected with goat anti-guinea pig IgGs conjugated to gold particles (1.4 nm in diameter; Nanoprobes, NY, USA, 1:100). After post-fixation (1% glutaraldehyde), the immunogold signal was enhanced with a silver enhancement kit (HQ silver, Nanoprobes; NY, USA). Ultrathin sections were examined with a transmission electron microscope (EM 912 OMEGA, ZEISS).
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6

Transmission Electron Microscopy Imaging

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Particles were adsorbed
from aqueous suspensions to carbon film Cu
TEM grids for 15 min. After the removal of the liquid with Kimwipe
paper, grids were washed with a drop of Milli-Q water to remove residual
salt precipitates. Standard imaging was performed on a Zeiss EM 912
Omega at an acceleration voltage (U) of 120 kV. High-resolution
imaging was performed on (i) a Jeol JEM 4010 transmission electron
microscope (U = 400 kV) and on (ii) an FEI Titan
80/300 scanning transmission electron microscope (U = 300 kV) equipped with a probe corrector, an EDX detector, and
an EELS spectrometer.
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7

Morphological Characterization of Pancreatic Cancer EVs

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The morphology of pancreatic cancer-derived EVs was assessed by transmission electron microscopy (TEM). In brief, EVs were put onto formvar-carbon-coated electron microscopy grids for 10 min in a wet chamber. After brief blotting the grid edge with filter paper, the grids were placed on drops of 2% aqueous uranyl acetate for 1 min, removed, blotted again, and placed on H2O drops for 1 min, removed, and blotted at the edge. After 24 h of air drying, the grids were inspected using a transmission electron microscope (Zeiss EM 912 Omega at 100 kV, Darmstadt, Germany).
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8

Transmission Electron Microscopy of Samples

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Samples were analyzed using a Zeiss EM 912 Omega (Zeiss, Oberkochen, Germany) transmission electron microscope equipped with a thermionic tungsten cathode, and a TRS slow scan CCD-camera for TEM (Tröndle Restlichtverstärker Systeme, Moorenweis, Germany). The images were taken at an acceleration voltage of 80 kV and processed using ImageSP ver.1.2.3.36 (SYS-PROG, Minsk, Belarus & Tröndle Restlichtverstärker Systeme, Moorenweis, Germany).
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9

Transmission Electron Microscopy Imaging

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TEM measurements were
performed on a Zeiss EM 912 Omega. The samples
were prepared by gently dropping the samples (20 μL) onto grids
and subsequent solvent evaporation in a dust-protected atmosphere.
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10

Transmission Electron Microscopy Protocol

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For transmission electron microscopy, the cells were washed in 0.1 M phosphate buffer, pH 7.4 and fixed in 2% glutaraldehyde for 1 h at room temperature. The samples were first washed in 0.1 M phosphate buffer and then in bidistilled water and finally postfixed in 1% osmium-bidistilled water for 1 h at room temperature. After washes in bidistilled water, the samples were dehydrated in increasing concentrations of ethanol, infiltrated in 1:1 ethanol:epon resin for 1 h and finally 100% epon resin for 48 h at 60 °C for polymerization. Seventy-nm-thick sections were cut with an ultracut UCT microtome (LEICA) and picked up on copper rhodium-coated grids. Grids were stained for 2 min in Uranyless (DELTA Microscopies) for 5 min in 0.2% lead citrate. Grids were analysed on an electron microscope (EM 912 OMEGA, ZEISS) at 80 kV, and images were captured with digital camera (Side-Mounted TEM CCD, Veleta 2kx2k). The software used is iTEM.
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