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Orius 600 digital camera

Manufactured by Ametek

The Orius 600 is a digital camera designed for laboratory applications. It features a high-resolution, scientific-grade image sensor capable of capturing detailed images. The camera is designed for reliability and ease of use in controlled laboratory environments.

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4 protocols using orius 600 digital camera

1

Characterizing Extracellular Vesicle Size and Morphology

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EVs were isolated from 3T3-L1, plasma, or lipid tissue as described above and suspended in PBS. A small aliquot of EVs was used for the measurement of the diameter by Dynamic light scattering zetasizer (Malvern, Worcestershire, UK). For transmission electron microscopy, EVs were adhered to 100 mesh Formvar and carbon coated grids for 5 min at room temperature. Grids were washed once with water, stained with 1% uranyl acetate (Ladd Research Industries, Williston VT) for 1 min, dried, and viewed by a JEOL 1200 EXII transmission electron microscope. Images were captured using a Gatan Orius 600 digital camera (Gatan, Pleasanton, CA).
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2

TEM Analysis of Extracellular Vesicles and Liver Samples

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For transmission electron microscopy, extracellular vesicles were adhered to 100 mesh Formvar and carbon coated grids for 5 minutes at room temperature. Grids were washed once with water, stained with 1% uranyl acetate (Ladd Research Industries, Williston VT) for 1 minute, dried and viewed using a JEOL 1200 EXII transmission electron microscope. Images were captured using a Gatan Orius 600 digital camera (Gatan, Pleasanton, CA). Liver samples were collected from the CDAA-fed mice after a short liver perfusion with 10 mL of 4% paraformaldehyde in 0.15 M sodium cacodylate buffer, pH 7.4 by using a 21 G needle. Samples were immersed in modified Karnovsky’s fixative (2.5% glutaraldehyde and 2% paraformaldehyde in 0.15 M sodium cacodylate buffer, pH 7.4) for at least 4 hours, postfixed in 1% osmium tetroxide in 0.15 M cacodylate buffer for 1 hour and stained en bloc in 3% uranyl acetate for 1 hour. Samples were dehydrated in ethanol, embedded in Durcupan epoxy resin (Sigma-Aldrich), sectioned at 50 to 60 nm on a Leica UCT ultramicrotome, and picked up on Formvar and carbon-coated copper grids. Sections were stained with 3% uranyl acetate for 5 minutes and Sato’s lead stain for 1 minute. Grids were viewed using a JEOL 1200EX II (JEOL, Peabody, MA) transmission electron microscope and photographed using a Gatan digital camera (Gatan, Pleasanton, CA).
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3

Characterization of Microvesicles from 3T3L1 and Plasma

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MPs were isolated from 3T3L1 or plasma described above and suspend in 1x PBS. For dynamic light scattering analysis, entire size was measured by Zetasizer nano ZS90 (Malvern). For Transmission electron microscope, MPs were adhered to 100 mesh Formvar and carbon coated grids for 5 minutes at room temperature. Grids were washed once with water, stained with 1% uranyl acetate (Ladd Research Industries, Williston VT) for 1 minute, dried and viewed using a JEOL 1200 EXII transmission electron microscope. Images were captured using a Gatan Orius 600 digital camera (Gatan, Pleasanton CA).
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4

Characterization of Extracellular Vesicles

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For dynamic light scattering analysis, entire size was measured by Zetasizer nano ZS90 (Malvern). For transmission electron microscopy, EVs were adhered to 100 mesh Formvar and carbon coated grids for 5 minutes at room temperature. Grids were washed once with water, stained with 1% uranyl acetate (Ladd Research Industries, Williston VT) for 1 minute, dried and viewed using a JEOL 1200 EXII transmission electron microscope. Images were captured using a Gatan Orius 600 digital camera (Gatan, Pleasanton CA).
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