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Orius 200 camera

Manufactured by Ametek
Sourced in United States

The Orius 200 camera is a scientific-grade digital camera designed for laboratory and research applications. It features a high-resolution CMOS sensor and advanced optics to capture detailed images and video. The camera's core function is to provide reliable and precise image acquisition for a variety of scientific and experimental tasks.

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5 protocols using orius 200 camera

1

Exosome Morphology Analysis by TEM and SEM

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Both transmission electron microscopy (TEM) and
scanning electron microscopy (SEM) were used to
assess the morphological features of the exosomes. First,
the exosomal pellet was fixed with 1% glutaraldehyde
(Sigma, USA) and then 20 μl of the fixed exosomes
were inserted on a carbon-coated grid and allowed to dry
at room temperature for 30 minutes. Then, a LEO 906
TEM (Zeiss, Germany) was used to each the samples
were washed twice with PBS for 5 minutes, and stained
with 1% uranyl acetate for 10 minutes before they were
visualized under a TEM at an accelerating voltage of 80
kV. DigitalMicrographsoftware (Gatan, Inc., Washington,
DC, USA) was used to record the TEM images that
were acquired with an Orius 200 camera (Gatan, Inc.,
Washington, DC, USA). We also assessed the particle
surface morphology by SEM. A total of 1 to 5 μl of the
dried sample was placed on a silicon chip, fixed with
2% paraformaldehyde and sputter-coated with gold-palladium, then visualised by SEM at 30 kV.
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2

Characterization of Colloidal Nanoparticles

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For each synthesis, a droplet of the as-produced colloidal solution is poured onto a 400-mesh copper grid covered with ultra-thin carbon on holey carbon support film (reference 01 824 from Ted Pella, Inc.). Transmission Electron Microscopy (TEM) experiments are carried out on a JEOL 2100 HT microscope operating at 200 kV. High resolution images are acquired using a Gatan Orius 200 camera and electronic diffraction patterns are analysed with the Digital Micrograph software from Gatan (see Fig. 3e and f). Selected area electron diffraction (SAED) patterns are averaged radially in order to obtain the diffraction pattern shown in Fig. 3b. Amorphous contribution of the carbon layer was approximated by an exponential and removed. Because a few thousands of particles are probed simultaneously, such a pattern can be interpreted as the powder pattern of the smallest nanoparticles (a few nanometers), even if contribution from larger particles are observed (see bright spots in the SAED from particles of a few tens of nanometers). As a consequence, such a pattern should be more considered as a fingerprint than a quantitative powder pattern. The size distribution in Fig. 2b is obtained from three different large field TEM images, including Fig. 2a. Nanoparticles were automatically detected with the plug-in Particles Sizer in ImageJ61 and diameters were deduced from their areas.
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3

Ultrastructural Analysis of Cell Monolayers

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Cells were chemically fixed in 2.5% (v/v) glutaraldehyde, 2% (v/v) paraformaldehyde in 0.1 M cacodylate (pH 7.2) buffer for 2h at room temperature, washed in cacodylate, post-fixed with 2% (w/v) osmium tetroxide supplemented with 1.5% (w/v) potassium ferrocyanide (45 min, 4°C), washed in water, dehydrated in ethanol (increasing concentration from 30 to 100%) and embedded in Epon as described in [31 (link)]. Ultrathin sections of cell monolayers were prepared with a Reichert UltracutS ultramicrotome (Leica Microsystems) and contrasted with uranyl acetate and lead citrate. Electron micrographs were acquired on a Tecnai Spirit Electron Microscope (ThermoFischer Scientific) equipped with a 4k CCD camera (EMSIS GmbH, Muenster, Germany) using ITEM software (EMSIS) or using a GATAN Orius 200 camera.
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4

Visualizing Bacterial Morphology by TEM

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10 ml of bacterial cell cultures at the onset of stationary phase (OD of 1) and after 24 h in BHI without or with 350 μM DIP were centrifuged (5000 x g) for 10 min at 4 °C. Cell pellets were washed twine with saline buffer and then 800 μl of glutaraldehyde solution 1% were added for fixing. Bacteria were visualized on 200-mesh nickel EM grids (mesh diameter of 74 μm) (Leica Microsystems, Wetzlar, Germany), coated with 2% Formvar (a polyvinyl formal resin) (Monsanto Chemical Company, St. Louis, MI, USA). All observations were performed at CMABio, the Center for Microscopy Applied to Biology (Caen, France) of Normandy University. Observations were performed on JEO1 1011 transmission electron microscopes operating at 80 kV. Images were acquired with a Gatan Orius 200 camera, and processed with Gatan Digital Micrograph software (Gatan, Pleasanton, CA, USA).
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5

Negative Staining of Extracellular Vesicles

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EV-enriched samples were visualized by TEM using the negative staining method. The sample was applied to Formvar-coated and carbon-stabilized copper grids and contrasted with a 1% (w/v) water solution of uranyl acetate. Samples were examined using a CM100 (Philips, Amsterdam, The Netherlands) transmission electron microscope, operating at 80 kV. Images were recorded with Orius 200 camera (Gatan) and processed by DigitalMicrograph software version 2.32 (Gatan Inc., Pleasanton, CA, USA).
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