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Tecnai g2 electron microscope

Manufactured by Olympus
Sourced in Germany

The Tecnai G2 is a high-performance electron microscope designed for advanced imaging and analysis. It features a LaB6 electron source, providing high beam brightness and excellent resolution for a wide range of materials. The Tecnai G2 is capable of operating in various imaging modes, including bright-field, dark-field, and scanning transmission electron microscopy (STEM).

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2 protocols using tecnai g2 electron microscope

1

Particle Uptake in Cell Cultures

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Sterilized discs (diameter 6 mm) were punched from transparent Melinex film (Plano, Wetzlar, Germany), treated with 70% ethanol for 30 min, dried, and placed into the wells of a microtiter plate. Cells were seeded (3 × 105 cells/well) in F-12 K medium with 5% serum and cultured on the discs. After 24 h, the medium was replaced by serum-free F-12 K medium containing 100 µg/mL of either PEBCA or PEBCA CBZ. Particle uptake was then continued for 4 and 16 h under cell culture conditions (37 °C, 5% CO2). Then, the cells were fixed with 2.5% glutardialdehyde in 0.1 M sodium phosphate buffer for 60 min. Cells were washed in PBS, post-fixed in 1% OsO4, stained en bloc with uranium acetate (1%), and embedded in Epon 812 (Sigma-Aldrich, Taufkirchen, Germany) as described earlier [20 (link)]. Isolated PEBCA particles were embedded in warm agar dissolved in phosphate-buffered saline (PBS) containing 3% bovine serum albumin and cooled on ice. Small pieces of the hardened mixture were embedded in Epon 812 and processed as described for the cells. Thin sections (50–60 nm) of all preparations were cut with a Reichert Ultracut microtome and viewed with a Tecnai G2 electron microscope at 120 kV. Digital images were taken with a Quemesa digital camera (Olympus Soft Imaging Solutions, Münster, Germany).
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2

Ultrastructural Analysis of Particle Treated Cells

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NR8383 cells were seeded onto small discs (diameter 6 mm) of Melinex film (Plano, Wetzlar, Germany) placed in the wells of a 96-well plate, subjected to particle treatment for 16 h as described in paragraph 2.4. Then, media were withdrawn and cells were immediately covered with 2.5% glutardialdehyde in 0.1 M sodium phosphate buffer (SPB, pH 7.3) for 60 min. Cells were washed three times with SPB, post-fixed in 1% OsO4, dehydrated in ethanol to the 70% step, and stained en bloc with uranium acetate (1%). Cells were dehydrated via ethanol/propylene oxide, and embedded in Epon 812 (Sigma Aldrich, Taufkirchen, Germany). Ultrathin sections (50–60 nm) were viewed with a Tecnai G2 electron microscope operated at 100 or 120 kV; images were taken with a Quemesa digital camera (Olympus Soft Imaging Solutions, Münster, Germany).
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