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Libra 120 plus ef tem transmission electron microscope

Manufactured by Zeiss

The Libra 120 PLUS EF-TEM is a transmission electron microscope (TEM) manufactured by Zeiss. It is designed to provide high-resolution imaging and analysis of materials at the nanoscale level. The instrument features an energy-filtering (EF) capability, which allows for the selective imaging of specific energy electrons, enhancing the contrast and resolution of the sample.

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2 protocols using libra 120 plus ef tem transmission electron microscope

1

Fabricating Biomimetic Nanoparticles from RBC Membranes

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To fabricate the nanoparticles, a previously reported membrane coating approach was employed.37 (link) First, poly(lactic-co-glycolic acid) (PLGA; carboxy-terminated, 50:50, 0.67 dL/g; Lactel Absorbable Polymers) cores were prepared by precipitating the polymer dissolved at 10 mg/mL using acetone into water, followed by evaporation to remove the organic solvent. Human RBC (hRBC) membrane ghosts were obtained by the hypotonic lysis of human O-negative RBCs (BioreclamationIVT). Human RBC membrane-derived vesicles were prepared by brief sonication of hRBC ghosts using a Fisher Scientific FS30D bath sonicator. To make hRBC-NPs, the membrane and PLGA cores were mixed together, followed by sonication to induce membrane fusion. Size and zeta potential were measured by dynamic light scattering (DLS) using a Malvern ZEN 3600 Zetasizer. To visualize the nanoparticles, the hRBC-NPs were deposited onto a 400-mesh carbon-coated copper grid (Electron Microscopy Sciences), stained with 1 wt% uranyl acetate (Electron Microscopy Sciences), and imaged using a Zeiss Libra 120 PLUS EF-TEM transmission electron microscope.
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2

Gastrointestinal Tract Ultrastructural Analysis

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The gastrointestinal tract was dissected into 2% EM-grade glutaraldehyde in PBS and fixed for 1 h at room temperature and then 2 h on ice. Samples were washed in PBS before embedding in soft agar. Tissues underwent secondary fixation in 1% osmium tetroxide plus 0.3% potassium ferricyanide. Guts were then en bloc stained with 2% uranyl acetate, dehydrated in ethanol, and embedded in EPON epoxy resin. For standard TEM, thin sections were mounted on slot grids and stained with uranyl acetate and lead citrate. Images were acquired using a Libra 120 PLUS EF-TEM transmission electron microscope (ZEISS) or a 100CX transmission electron microscope (JEOL). For tomographic studies, both sides of semi-thick sections were coated with gold particles and tilt series collected using an FEI Titan 80–300 (CTWIN) IVEM/STEM. Tomographic reconstructions and 3D models of mitochondria were generated with IMOD and TxBR.
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