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Tecnai g2 spirit tem microscope

Manufactured by Thermo Fisher Scientific
Sourced in United States, Czechia

The Tecnai G2 Spirit TEM microscope is a transmission electron microscope designed for high-resolution imaging and analysis of a wide range of materials and samples. It features a LaB6 electron source, advanced optics, and a robust, stable design to enable detailed structural and compositional characterization at the nanoscale.

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6 protocols using tecnai g2 spirit tem microscope

1

Negative Stain TEM of Biomolecular Samples

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For negative-stain TEM, 5 µl of sample was pipetted onto a glow-discharged copper grid coated with parlodion and carbon and left to adsorb for 1 min at RT. The grid was then washed with 4 droplets of nanopure water, and subsequently stained with 2 % uranyl acetate for 10 s, blotting between each step. Grids were scanned using a Tecnai G2 Spirit TEM microscope with a LaB6 filament operated at 120 kV (FEI Company, Eindhoven, The Netherlands). Images were recorded by a side-mounted EMSIS MORADA camera.
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2

Phosphotungstic Acid Polymer Staining

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A phosphotungstic acid (PTA) solution was used as a positive and a negative staining agent because of its preferential interaction with the ester groups on the poly-MPC polymers. The PTA staining solution was prepared by dissolving 37.5 mg of PTA in boiling distilled water (5 mL). The pH was adjusted to 7.4 by adding a few drops of 5 M NaOH with continuous stirring. The PTA solution was then filtered through a 0.2 µm filter. 5 µL of polymersome/PBS dispersion was deposited onto glow-discharged copper grids. After 1 min, the grids were blotted with filter paper and then immersed into the PTA staining solution for 5 s for positive staining and 10 s for negative staining. Then, the grids were blotted again and dried under vacuum for 1 min. Grids were imaged using an FEI Tecnai G2 Spirit TEM microscope at 80 kV (FEI Company, Hillsbro, OR, USA).
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3

Polymersome Staining with PTA

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A PTA solution was used as a positive and a negative staining agent because of its preferential interaction with the ester groups on the PMPC polymers (54 ), which are not present in the PEO-PBO copolymer. The PTA staining solution was prepared by dissolving 37.5 mg of PTA in boiling distilled water (5 ml). The pH was adjusted to 7.4 by adding a few drops of 5 M NaOH with continuous stirring. The PTA solution was then filtered through a 0.2-μm filter. Then, 5 μl of polymersome/PBS dispersion was deposited onto glow-discharged copper grids. After 1 min, the grids were blotted with filter paper and then immersed into the PTA staining solution for 5 s for positive staining and 10 s for negative staining. Then, the grids were blotted again and dried under vacuum for 1 min. Grids were imaged using an FEI Tecnai G2 Spirit TEM microscope at 80 kV.
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4

Negative Staining of Polymersomes

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Conventional TEM imaging was performed using an FEI Tecnai G2 Spirit TEM microscope at 80 kV equipped with an Orius SC1000 camera. The polymersomes were stained using a PTA solution at 0.75% (w/v). PTA at 10% (w/v), supplied by Sigma-Aldrich, was used. The solution was prepared by dissolving 37.5 mg of PTA in boiling distilled water (5 ml). The pH was adjusted to 7.0 by adding a few drops of 5 M NaOH under continuous stirring. The PTA solution was then filtered through a 0.2-μm filter.
Copper grids were glow-discharged for 40 s to render them hydrophilic. Then, 5 μl of polymersome/PBS dispersion (diluted 10-fold; concentration, 0.5 mg/ml) was deposited onto the grids for 1 min. Then, the grids were blotted with filter paper and immersed in the PTA staining solution for 5 s for negative staining. The grids were blotted again and dried under vacuum for 1 min.
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5

Transmission Electron Microscopy of Mouse Thyroid

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Mouse thyroid tissue was fixed in 2.5 % Gluteraldehyde, 0.1 M Phosphate Buffer at pH 7.4 for TEM microscopy. The tissue sections were imaged on FEI Tecnai G2 Spirit TEM microscope.
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6

Characterization of Magnetic Nanoparticles

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Transmission electron microscopy was used to measure the number-average particle diameter (Dn) and the particle size distribution (dispersity Ð) using a Fei Tecnai G2 Spirit TEM microscope (Brno, Czech Republic). The size of mag.SLPs was evaluated using a MAIA3 scanning electron microscope (Tescan; Brno, Czech Republic). Dynamic light scattering (DLS) of aqueous SLP dispersions (25°C) on a Zen 3600 Zetasizer (Malvern Instruments; Malvern, UK) was used to determine ζ-potential, hydrodynamic diameter (Dh), and polydispersity index (PDI) from the intensity distribution curve. Iron content was determined using a Perkin Elmer 3110 atomic absorption spectrometer (AAS; Waltham, MA, USA), content of C was measured on a FlashSmartTM elemental analyzer (Thermo Fisher Scientific; Waltham, MA, USA), and thermogravimetric analysis was performed in air flow with 10°C/min heating rate on a Perkin Elmer TGA 7 thermogravimetric analyzer (Waltham, MA, USA) equipped with Pyris software. The heat effect of the mag.SLPs was tested under an alternating magnetic field (AMF) by homemade AC system and temperature changes were monitored by a fiber optic temperature sensor (FISO Technologies; Québec, Canada) (Skumiel et al., 2016 (link)). Magnetization of dry particles was determined using an EV9 vibrating sample magnetometer (DSM Magnetics, ADE Corp.; Lowell, MA, USA) at RT.
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