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Tecnai 12 biotwin transmission

Manufactured by Thermo Fisher Scientific
Sourced in Netherlands

The Tecnai 12 BioTWIN is a transmission electron microscope designed for biological applications. It provides high-resolution imaging and analysis capabilities for a variety of samples. The core function of the Tecnai 12 BioTWIN is to magnify and visualize the internal structure of biological specimens, enabling researchers to study their morphology, ultrastructure, and other characteristics at the nanoscale level.

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3 protocols using tecnai 12 biotwin transmission

1

Visualizing Mycobacteriophage D29 Infection

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The interaction between the mycobacteriophage D29 and its host strain was examined by transmission electron microscopy. Infection was performed at an MOI of 1. Samples collected at different stages of infection were negatively stained with 2% uranyl acetate and examined under an FEI Tecnai 12 Biotwin transmission electron microscope (FEI, Netherlands) at an accelerating voltage of 100kV.
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2

Tick Gut Ultrastructure and Protein Localization

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Transmission electron microscopy was performed as indicated (Kariu, Smith, et al., 2013 (link)). Briefly, the dissected guts from 48-hour fed ticks were fixed with 2.5% glutaraldehyde in 0.1 M sodium cacodylate buffer (pH 7.4), followed by 1% osmium tetroxide in 0.1 M sodium cacodylate buffer. Grids were embedded in 0.67% uranyl acetate in 1.8% methylcellulose and examined on a FEI Tecnai 12 BioTWIN transmission electron microscope. For confocal microscopy, the tick organs were dissected and fixed in acetone for 10 min. The sections were blocked with PBS with 5% goat serum and then labeled with anti-PM_CBP antibody (1:100 dilution), followed with Alexa Fluor 488-labeled goat anti-mouse IgG (Invitrogen). The cell nuclei were stained either with propidium iodide (PI, red) or DAPI (blue). Finally, the slides were washed using PBS with 0.05% Tween 20 and imaged by a LSM 510 laser confocal microscope (Zeiss), as described (Kariu, Smith, et al., 2013 (link)).
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3

Mitochondria-ER Contacts in Human Cells

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Ultrathin sections from human biopsies were processed using Leica Ultracut UCT (Leica, Vienna, Austria) and contrasted with uranyl acetate and lead citrate. Sections were observed with a Tecnai 12 BioTWIN transmission electron microscope (FEI Company, Eindhoven, The Netherlands) at 100 kV. Digital images were acquired with a Veleta camera (Olympus Soft imaging Solutions, GmbH, Münster, Germany) at a primary magnification of 20.500×.
Pictures were acquired as before [6 (link)]. Briefly, 10 random cells were chosen per patient and, for each cell, pictures of all visible mitochondria were taken. In total, 140 cells were analysed, including more than 800 MERCS and 2000 mitochondria. The number of MERCS and mitochondria as well as MERCS length and mitochondria perimeter were obtained using iTEM FEI software (EMSIS GmbH, Muenster, Germany). MERCS were considered as such when the distance between ER and mitochondria was equal or bellow 30 nm. Values presented in Additional file 1: Table S1 represent average values per cell profile per patient. The overall quality of the tissue was very high and representative images are shown. In particular, the structure of mitochondria was very well preserved while the ER structures sometimes appeared dilated.
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