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208hr high resolution sputter coater

Manufactured by Cressington
Sourced in United Kingdom, United States

The 208HR high-resolution sputter coater is a laboratory equipment designed for the deposition of thin films onto various substrates. It is capable of producing high-resolution coatings with precise thickness control. The core function of this device is to facilitate the sputter coating process, which is a commonly used technique in materials science, nanotechnology, and other related fields.

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20 protocols using 208hr high resolution sputter coater

1

Scanning Electron Microscopy of Bivalve Shells

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Scanning electron microscopy (SEM) was used to determine fine-scale shell valves features for the taxonomic description and the presence of bacteria associated with the gill. For SEM imaging of soft tissues and hard parts, samples were dissected, critical point dried using the Samdri PVT-3D critical point dryer (Tousumis, Maryland, USA), mounted on a standard aluminium SEM stub and coated with platinum to a thickness of 5 nm using the Cressington 208 HR High Resolution Sputter Coater (Cressington Scientific Instruments, Hertfordshire, UK). Samples were imaged on the Hitachi S-4800 field emission scanning electron microscope. Gill tissues were manually fractured using a razor blade prior to coating to expose bacterial symbionts.
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2

Structural Fiber Surface Observation

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The surfaces of the structural fibers were observed by Scanning electron microscope (SEM) imaged with FE-SEM Thermo Scientific Quattro S completed with EDS Detector, WetSTEM, Heating Stage, and Tensile Stage. The samples were coated with gold using a Cressington 208HR High-Resolution sputter coater (Cressington Scientific Instruments, Watford, UK). Magnification of 100–10,000 times until the surface object was visible.
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3

Dry ECM Iridium Sputter Coating

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Dry ECM was iridium sputter coated with a Cressington 208HR high-resolution sputter coater (Cressington). Samples were imaged and EDS was performed using a FEI-Quanta 600 FE-SEM (Thermo Fisher Scientific).
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4

Scanning Electron Microscopy of Shell Valves

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Shell valves (Fig. 4) were removed and dehydrated in absolute ethanol, critical-point dried using the SAMDRI-PVT-3D Critical Point Dryer (Tousumis, Rockville, MD), mounted on a standard aluminum scanning electron microscope stub, and coated with platinum to a thickness of 5 nm, using the Cressington 208 HR High Resolution Sputter Coater (Cressington Scientific Instruments, Watford, United Kingdom). Images were produced on the Hitachi S-4800 field emission scanning electron microscope (Krefeld, Germany).
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5

Nonwoven Fiber Diameter Analysis

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The SEM images of the nonwovens were acquired by the Zeiss LEO 1530 (Gemini, Germany) scanning electron microscope equipped with a field emission cathode and a secondary electron (SE2) and an Inlens detector. An acceleration voltage of 3 kV and a working distance between 5 and 6 mm were used. Before the measurement, the nonwoven samples were cut into small pieces and attached to a sample holder with conductive double-sided tape. The samples were subsequently sputter-coated with a 2.0-nm platinum layer by a Cressington 208HR high-resolution sputter coater, equipped with a quartz crystal microbalance thickness controller (MTM˗20). From 50-diameter measurements with the software ImageJ, an average value and the standard deviation of the fiber diameter were calculated.
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6

Synthesis of Pt-Coated Polystyrene Particles

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Spherical latex particles based on polystyrene (2% cross-linked) with diameter (2.00 ± 0.05) μm, i.e., size polydispersity 2.5%, were purchased from Sigma Aldrich. Pt-half-coated particles were produced through physical vapor deposition46 (link),47 (link) as follows: particles were spin coated from ethanol on glass slides at sub-monolayer concentrations and subsequently sputter coated from above with a (4.7 ± 0.2) nm Pt layer (Pt/Pd 80/20, MicrotoNano70-PPS708) using a standard sputter coating system (Cressington 208HR High Resolution Sputter Coater). The particles were redispersed in water by sonication and were subsequently washed and stored in water.
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7

Scanning Electron Microscopy of Fungal Growth and Straw Decay

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The growth of fungal mycelia and the degree of straw decay in solid fermentation samples inoculated with A. fumigatus Z5 spores for 4 days were observed by scanning electron microscopy. The rice straw in the solid fermentation sample was first collected, cut into a certain size with a sharp blade and washed [52 ], and then fixed with a fixing solution (2.5% glutaraldehyde), followed by dehydration using increasing concentrations of ethanol (from 20 to 98%, v/v) and acetone (from 30 to 90%, v/v); finally, the critical point dryer (HCP-2, Hitachi High-Technologies Corporation, Japan) was used to critically dry the sample and a layer of nanometer thick Au/Pd alloy layer was sprayed using a Cressington 208 HR high-resolution sputter coater (Cressington, UK). Imaging can be performed using the Hitachi S-4800 FE-SEM (Hitachi, Japan) after sample preparation.
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8

Scanning Electron Microscopy Analysis of PC-Coated Fabrics

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Morphological analyses of the PC-coated fabrics were carried out by scanning electron microscopy with an ultra-high resolution field emission gun (FEI NOVA 200 Nano SEM). Before all measurements, the PC-coated fabric samples were covered with a thin film of gold/palladium (80:20) in a 208HR high-resolution sputter coater (Cressington, Watford, UK) coupled to an MTM-20 high-resolution thickness controller (Cressington, Watford, UK).
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9

Scanning Electron Microscopy of Berry Surfaces

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Berry sections were mounted onto SEM stubs, dried, and sputter coated using a Cressington 208HR High Resolution Sputter Coater with 12 nm Au/Pd. The images were taken using a Hitachi S-4700 Field Emission scanning electron microscope with 5 kV acceleration voltage at 10 µA and a working distance of 15 mm at a tilt of 34°. For the developmental time course, only CT berries (one berry per time point) were analyzed. For the comparison between CT and WD berries, only samples collected at 113 DAA (late ripening) were analyzed. Three biological replicates (one berry per biological replicate) per treatment were imaged. For each sample analyzed, images were taken from at least three different areas of the berry surface.
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10

Electrospinning PLATMC Nanofibers on 3D Scaffolds

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Nanofibers
were prepared using an in-house-made electrospinning machine. After
solvent optimization, a 75:25 solvent mixture of 2,2,2-trifluoroethanol
(TFE) and chloroform was used to dissolve poly(l-lactide-co-trimethylene carbonate) (PLATMC, kindly provided by Novus
Scientific AB, Sweden) (Mn ∼ 220
kg mol–1) (10% w/v). A 5 mL syringe was filled with
the solution and then pumped (Harvard apparatus, USA) at a flow rate
of 5 mL h–1 through a 22-gauge size at a voltage
of 15 kV. The 3D-printed PCLDX scaffolds were placed on a plate collector,
and nanofibers were collected onto the scaffolds for 5 min. The 3D
printed PCLDX scaffolds with nanofibers were splutter coated with
Pt:Pd using a Cressington 208HR High Resolution Sputter Coater with
a Pt:Pd target before micrographs of the nanofibers were taken with
a high field emission scanning electron microscope S-4800 (SEM) (Hitachi,
Japan) and then processed with ImageJ (NIH, USA.).
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