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208hr high resolution sputter coater

Manufactured by Ted Pella
Sourced in Canada, United States

The 208HR High Resolution Sputter Coater is a laboratory equipment designed for the deposition of thin conductive films on various substrates. It is primarily used to prepare samples for high-resolution microscopy techniques, such as scanning electron microscopy (SEM) and transmission electron microscopy (TEM).

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5 protocols using 208hr high resolution sputter coater

1

SEM Characterization of PPDO Sutures

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The morphologies of the treated PPDO sutures were examined by scanning electron microscopy (SEM). All suture samples were deposited on a conductive tape. A Nova NanoSEM 230 SEM (FEI, Hillsboro, OR) equipped with an EDX detector (the Octane Silicon Drift Detector (SDD), EDAX Inc., Mahwah, NJ) was used in Fig. 2B and C. All imaging (working distance of 5 mm, acceleration 5–10 kV) was done at room temperature and in a high vacuum (5E-6 Torr). SEM samples were coated with 3 nm Pt/Pd on a 208HR High Resolution Sputter Coater (Ted Pella, Inc., Redding, CA) and the images were obtained at a spot size 3. SEM-EDX samples were uncoated and the images were obtained at a spot size 4.
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2

Nanoparticle Morphology Analysis by SEM

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Morphology study of the nanoparticles was carried out using scanning electron microscopy (SEM) (4 (link)). The formulation was lyophilised and further dried using vacuum oven for 30 min and the powder was uniformly spread on the coverslip and further coated with platinum using 208HR High-Resolution Sputter Coater (Ted Pella, INC, CA, USA). Coated sample was then inserted into the specimen chamber and scanned using TM 3030 Plus scanning electron microscope (Hitachi, Tokyo, Japan), at 5 kV.
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3

Characterization of Porous Polymer Scaffolds

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Samples of the scaffolds were coated with platinum and palladium for 2 minutes at 0.08 mbar and 300 V (208HR high resolution sputter coater, Ted Pella Inc, Redding, CA) for scanning electron microscopy (EVO MA10, Carl Zeiss, Thornwood, NY). Porosity was calculated using gravimetric measurements. Porosity, ε, is defined in terms of the apparent density of the fiber mat, ρAPP and bulk density of the polymer, ρPU of which it is made: ε = 1 − ρAPP/ρPU. The apparent scaffold density ρAPP was measured as mass to volume ratio on 10 mm dry disks: ρAPP = Mass/VPU. 10 mm × 40 mm samples of scaffold were mounted on an electromechanical load frame and tensile testing was performed using a 1 kN load cell and pneumatic tensile grips (30 mm gauge tested at 1 mm/sec, Instron 5943 Apparatus, Instron, Norwood, MA).
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4

Microparticle Characterization via SEM Imaging

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The microparticle geometry and size were determined using a field emission scanning electron microscopy (SEM) (S-4100T, Hitachi High Technologies America, Inc., Pleasanton, CA, USA). Particles were immobilized to a double-sided carbon tape (Ted Pella Inc, Redding, CA, USA) supported by an Al stub (Ted Pella Inc. Redding, CA, USA). After coating the particles with 10 nm of gold using a sputter coater (208 HR High Resolution Sputter Coater, Ted Pella Inc., Redding, CA, USA), the samples were transported to the SEM vacuum chamber. The typical acceleration voltage and emission current used in this work were 2 kV and 10 μ A, respectively. The SEM images were loaded into Image J (National Institutes of Health, Bethesda, MD, USA), where the size of the microparticles was determined using the geometrical Feret diameter ( dg ).
The aerodynamic diameter ( da ) was calculated using Equation (3), following published method [32 (link)]. The tapped density ( σ ) was measured using established protocols [32 (link)], where the particle containers were tapped on a hard surface for 1000 taps. The reference density ( ρ ) is 1 g/mL, which is the standard reference for the diameter of a spherical particles that has the same vertical velocity as the particle of interest [34 (link)].
da=dgσρ
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5

High-Resolution Imaging of Murine Uterine Epithelium

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To analyze the surface of the luminal uterine epithelium, uteri were harvested from mice at 3.5 dpc and flushed with 0.5 ml of PBS to remove blastocysts and debris. The uteri were then dissected longitudinally under a dissecting microscope with spring scissors and immediately submerged in ice-cold 2.5% glutaraldehyde in PBS overnight at 4 °C. The tissues were washed extensively in PBS and gradually dehydrated in a series of EtOH solutions for 15 min incubation times and stored in 100% EtOH. The tissues were then dried in an Autosamdri-815 (Tousimis Research Corporation) critical point dryer for 1.5 h. To enhance the SEM image contrast, the samples were coated with a thin iridium film of 7 nm with a magnetron sputtering coater (208HR High Resolution Sputter Coater, Ted Pella, Inc). Images of the uterus were collected in a Nova Nano SEM (FEI) with a working distance of 5 mm at room temperature in a high vacuum (2E−6 Torr) at the Houston Methodist Hospital TEM Microscopy Core.
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