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16 protocols using titan3

1

Size Exclusion HPLC of Hemoglobin and Lactoferrin

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hHb and LtEc samples were separated on an analytical Acclaim SEC-1000 (4.6 × 300 mm) column (Thermo Fisher Scientific, Waltham, MA) as previously described in the literature [19 (link)]. The mobile phase consisted of 50 mM sodium phosphate buffer (PB) at pH 7.4. Chromeleon 7 software was used to control HPLC parameters such as flow rate (0.35 mL/min), UV-visible absorbance detection (280 nm [to detect total protein] and 413 nm [to detect heme]). All samples were filtered through 0.2 μm syringe filters (Titan3, Thermo Fisher Scientific, Waltham, MA) before size exclusion (SEC) HPLC analysis.
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2

Characterizing Se Distribution in PbBi2(Te1-ySey)4

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To investigate the Se distribution, TEM samples of the PbBi2(Te1-ySey)4 (y = 0.5) for [100] cross-sectional observation were prepared using conventional methods including mechanical polishing, dimple grinding and Ar ion polishing. STEM observation was performed using a 300-kV aberration-corrected electron microscope (Thermo Fisher Scientific, Titan3).
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3

Quantification of Neurotransmitters and Metabolites

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Frozen tissues were weighed then sonically disrupted in 200 μl of 200 mmol/l HClO4 before being centrifuged for 10 min at 13 000 rpm at 4°C to remove cellular debris. Next, the samples were filtered through 0.22 μ Thermo Scientific Titan3 (Waltham, Massachusetts, USA). Cellulose Acetate Syringe Filters. A 100 μl aliquot of the supernatant was placed in a WPS-3000TBSL autosampler maintained at 10°C and 10 μl were injected onto a Thermo Scientific Hypersil BDS C18 column using a Thermo Scientific Dionex Test Phase as the mobile phase (flow rate of 0.5 ml/min). Coulometric detection was accomplished with a Thermo Scientific Dionex 6011RS ultra Coulometric Analytical cell and the signal was analyzed using Thermo Scientific Chromeleon 7.2 Chromatography Data System software. Absolute tissue concentrations (ng/mg) for dopamine, serotonin, and norepinephrine was determined by comparison with external standard curves and corrected for tissue weight. Identical procedures were used to quantify concentrations of the metabolites of dopamine, 3,4-dihydroxyphenylacetic acid (DOPAC), and of serotonin, 5-hydroxyindoleacetic acid (5-HIAA).
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4

Soluble Mucus Components Analysis

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Static light scattering for soluble components of SMG and HBE mucus were performed on a research goniometer (BI-200SM, Brookhaven Instruments), equipped with a 640-nm laser. A series of solutions with different concentrations were measured at scattering angles between 40° and 150°. The data were plotted as a Zimm plot, from which the radius of gyration (Rg) of the solutes was extracted. The log-normal size distribution of the solutes was obtained by cumulant analysis of the correlation function between 100 ns and 10 ms. Before measurements, all solutions were filtered through a 0.45-μm hydrophilic polyvinylidene difluoride syringe filter (Titan 3, Thermo Fisher Scientific) to remove dust particles and large cell debris.
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5

Nanoparticle Dispersion for OSC Fabrication

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CCO and Mg:CCO nanoparticles were dispersed into 2-MOE to make 2 mg mL−1 suspensions for materials characterization and fabrication of P3HT:PC61BM OSCs, PFBT2Se2Th:PC71BM OSCs, PTB7-Th:ITIC OSCs, and MAPbI3 PSCs. Just prior to film preparation, the suspensions were placed into a bath sonicator (Branson 3510, Plano, TX, USA) for 90 min, then filtered through a 1 μm PTFE filter (Thermos scientific, Titan3, Houston, TX, USA), re-sonicated for 90 min, and again filtered through a 0.45 μm PTFE filter (Biomed Scientific, Seattle, WA, USA).
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6

Quantification of 6-Gingerol and 6-Shogaol in Ginger Extracts

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The stock solution of 1 gL -1 ppm of 6-gingerol and 6 -shogaol (Chengdu Biopurify Phytochemicals Ltd., China) were prepared in HPLC grade methanol. The stock solution was then serially diluted into 0.05 -0.5 gL -1 of working solutions for the calibration curves at five concentration levels and were filtered through 0.20 mm syringe filter (Titan 3, Thermo Scientific). A volume of 10 mL of standard solutions was injected into HPLC system. The calibration curves were established by the peak areas and concentrations of working solutions.
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7

Real-Time Reconstruction with Advan-TEM

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For real-time reconstruction, the data was acquired with a probe corrected Thermo Fisher Titan 3 (X-Ant-TEM), operated at 300 kV with a convergence angle of 20 mrad. The CBEDs are collected with a MerlinEM direct electron detector (Ballabriga et al., 2011) . The zeolite datasets are acquired with Thermo Fisher Themis Z (Advan-TEM) at 200 kV and a custom made Timepix3 detector (Poikela et al., 2014) based on an Advapix TP3 camera unit, with a convergence angle of 12 mrad.
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8

Imaging Gold Nanoparticle Aggregates

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TEM images of gold NP aggregates on a holey carbon film (Agar Scientific AGS147) were taken in a FEI Titan3 scanning transmission electron microscope operated at 300 kV, in which a small probe (~0.1 nm in diameter) was rastered across the sample and the scattered electron beam collected by an annular detector (annular dark-field imaging). With a sufficiently high inner collection angle (>60 mrad) of the high-angle annular dark-field image, the scattered intensity is largely incoherent (there are no contrast reversals) and intensity may be readily interpreted: when the atomic columns of a crystal are aligned with the electron beam, the bright peaks correspond to the atomic columns. Low Z elements or thin regions appear darker and the vacuum is black (zero intensity). A Hitachi S-5500 in-lens field emission scanning electron microscope was used to acquire scanning electron microscopy images of gold NP aggregates deposited on a p-doped silicon wafer (Sigma-Aldrich 647764) and gold NP dimers on an ITO-coated coverslip (acceleration voltage 3 kV).
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9

Characterization of ReS2/WS2 heterostructures

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Scanning electron microscope images were taken by Zeiss Sigma. Optical images were taken with an optical microscope (Olympus DX51). Raman spectroscopy and photoluminescence with an excitation wavelength of 532 nm were carried out using a Renishaw inVia. The atomic force microscope images were collected on an NT-MDT Ntegra Spectra. The ReS2/WS2 was transferred onto the 300 nm SiO2/Si for such measurements. X-ray photoelectron spectroscopy was performed on a Thermo Scientific, ESCALAB 250Xi. The measuring spot size was 500 μm and the binding energies were calibrated by referencing the C 1 s peak (284.8 eV). The TEM images were taken with an aberration corrected, high-resolution TEM (AC-HRTEM, FEI Titan3 (link)) operating at 80 kV. X-ray diffraction measurements were performed using a Rigaku MiniFlex600 with Cu–Ka radiation over the range of 2θ=10∼80°.
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10

High-Resolution Atomic Imaging

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Aberration-corrected high-resolution scanning transmission electron microscopy (HR-STEM) images were collected using a double aberration-corrected FEI Titan3 (60–300) operating at 80 kV at Penn State. All high-resolution STEM images are captured with a high angle annular dark field (HADDF) detector. A beam current of 45 pA, beam convergence of 30 mrad, and camera length of 115 mm are used for image acquisition.
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