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57 protocols using milli q advantage a10 water purification system

1

Cardiovascular Disease Diagnostic Protocol

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The following instruments were used in the study: percutaneous transluminal coronary angioplasty (PTCA) balloon dilatation catheter (specification: 3.0 × 20, Cordis); 8F catheter (Beijing Wandong Kuli’aite Medical Products); Finesse 325 manual microtome, Histocentre 3 tissue embedding machine, and Excelsior ES tissue processor (Thermo Scientific); BX51 microscope (Olympus); Varistan Gemini automated slide stainer (Thermo Scientific); Pressure gauge (Shanghai Medical Instruments); TB-215D electronic analytical balance [Denver Instruments (Beijing)]; rat fixing frame (Beijing Huamei Plexiglass Products); Waters ACQUITY Xevo TQ-XS UPLC/MS System with Masslynx v4.1 (Waters, United States); MSU225S-000-DU semi-microelectronic analytical balance (Sartorius, Germany); VX- III multi-tube vortexer (Beijing Tarjin Tech); NA-5L hybrid nitrogen generator (Beijing ZTE Technology Development); Micropipettes and Centrifuge 5424R low-temperature high-speed centrifuge (Eppendorf, Germany); KQ250E ultrasonic cleaner (Kunshan Ultrasonic Instruments); Milli-Q Advantage A10 water purification system (Millipore, United States).
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2

Ritonavir Polymorphic Form II Characterization

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Ritonavir (Polymorphic Form II) was obtained from Anhui Biochem United Pharmaceutical Co., Ltd. (Hefei, China) that was used without further purification. Ritonavir Reference Standard (99.3%) was purchased from The United States Pharmacopeial Convention (North Bethesda, MD, USA). PVPVA (Kollidon® VA 64) was supplied by BASF Corporation (Ludwigshafen, Germany). Sorbitan monolaurate (Span 20-LQ-(AP)) was obtained from Croda Inc. (East Yorkshire, UK). The ultrapure water was purified by the Milli-Q® Advantage A10® water purification system (Millipore, MA, USA). Acetonitrile of high performance liquid chromatography (HPLC) grade was obtained by Thermo Fisher Scientific (Newington, NH, USA). Methanol was provided by Adamas Pharmaceuticals, Inc. (Shanghai, China). Potassium dihydrogen phosphate and phosphoric acid were supplied from Tianjin Zhiyuan Chemical Reagent Co., Ltd. (Tianjin, China).
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3

Fluorescent Hydrogel Synthesis Protocol

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Acrylamide (AAm), N-hydroxysuccinamide, 4’Aminofluorescein isomer I, 5(6)-Carboxyfluorescein, Fluorescein disodium salt, FITC, 3-(trimethoxysilyl) propyl methacrylate and Ethylene glycol were purchased from Acros Organics. Pyruvic acid and 3-aminopropyl methacrylamide hydrochloride (3AP) were purchased from Sigma-Aldrich. Tetramethylethylenediamine (TEMED) was purchased from ThermoScientific. Ammonium persulfate (APS) was purchased from Aqua Solutions. Polyethylene(glycol) diacrylate (PEGDA; Mw = 400) was purchased from PolySciences Inc. 1-Ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) was purchased from Advanced Chemtec. Hydrochloric acid (37.5%) and glycine were purchased from Fisher Scientific. Glass microscope slides (3” × 1” × 1.2 mm) were purchased from Fisherbrand. Ethanol (EtOH) was purchased from Decon Laboratories Inc. Water (dd-H2O) was deionized using Milli-Q Advantage A-10 water purification system (Millipore, U.S.A.). When required, degassing was performed by sparging with a continuous argon stream for 15 min for small volumes and 2 h for large volumes. Coverglass slips (Thickness #1, Diameter 25mm) were purchased from Electron Microscopy Sciences. Rain-X hydrophobic spray manufactured by ITW (Global Bands, TX) was purchased from Home Depot.
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4

Comprehensive Metabolite Profiling Protocol

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Uric acid, L-tryptophan, L-alanine, L-valine, L-leucine, L-isoleucine, glycine, l-serine, succinic acid, fumaric acid, malic acid, 2-ketoglutaric acid, L-glutamic acid, D-ribose, sodium 2-hydroxybutyrate, 3-hydroxybutyric acid, 2-isopropylmalic acid, formic acid, serotonin, γ-aminobutyric acid-2,2,3,3,4,4d6, 21-deoxycortisol, 11-deoxycortisol, oleic acid, cis-4,7,10,13,16,19-docosahexaenoic acid, cis-10-nonadecenoic acid (C19:1n9c) and sodium taurochenodeoxycholate were purchased from Sigma-Aldrich (St. Louis, MO, USA). Taurocholic acid was obtained from Steraloids (Newport, RI, USA). p-Cresyl sulfate potassium salt and arachidonic acid were supplied from Toronto Research Chemicals (North York, ON, Canada). Urea, HPLC-graded acetonitrile, methanol and isopropanol were obtained from Fisher Scientific (Hampton, NH, USA). Water was purified in-house using a Milli-Q Advantage A10 water purification system (Millipore, Bedford, MA, USA). Palmitic acid, cis-9,12-linoleic acid, 2-aminobutyric acid, pyridine (HPLC grade) with AcroSeal and N-methyl-N-(trimethylsilyl) trifluoroacetamide (MSTFA) were acquired from Acros Organics (Morris Plains, NJ, USA).
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5

Sensitive Magnetic Bisphenol A Sensor

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DES, APBA, 3-aminopropyl triethoxy silane (APTES), and tetraethyl orthosilicate (TEOS) were purchased from J&K Scientific Ltd. Glutaraldehyde (GA), FeCl3·6H2O, FeCl2·4H2O, potassium peroxydisulfate, and other reagents were obtained from Beijing Chemical Reagent Company (Beijing, China). Bisphenol A was from Chengdu Xiya Chemical Co., Ltd. (Chengdu, China). Phenol, bisphenol F, estrone, and estradiol were provided by Tianjin Chemical Reagent Co. Ltd (Tianjing, China). All reagents were of analytical grade. Acetonitrile (ACN) for HPLC was of HPLC-reagent grade and was supplied by J&K Scientific Ltd. (Beijing, China). All solutions were prepared with ultrapure water (Milli-Q Advantage A10 Water Purification System, Millipore Corporation, France). DES (100 mg) was dissolved in 100 mL of ethanol for the preparation of 1000 mg L−1 of DES stock solution, and stored at 4 °C until use. DES solutions with required concentration could be diluted with ultrapure water for further use. The elution solution was a mixture of methanol-0.1 M acetic acid (5.0 mL, v/v, 9/1).
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6

Analytical Techniques for Compound Characterization

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Fluorimetry studies were performed on a Photon Technology International fluorimeter with lamp power supply model LPS-220B, motor driver model MD-5020, and shutter control model SC-500. 1H-NMR studies were performed on a Bruker AV-III 400 MHz NMR spectrometer with ICON NMR in automation, while 13C NMR studies were run at 100 MHz. CDCl3 was used as solvent, chemical shifts are reported in ppm, while coupling constants, J, are reported in Hertz. Multiplicities in the spectra are represented by d (doublet), t (triplet), m (multiplet), and b (broad). High-resolution mass spectra (HRMS) were recorded using a Waters Synapt G2; spectra are reported as m/z (relative intensity). 1 μL of saturated LiCl in acetonitrile was added to 50 μL of sample, masses are reported for either [M+] or [M+H+] ion. Millipore water was obtained from a Milli-Q Advantage A-10 water purification system (MilliPore, USA). Microscopy images were captured using a Zeiss Axio Imager A2. Nanoparticle Tracking Analysis was performed on a Malvern NanoSight LM10.
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7

Synthesis and Purification of Phenanthrenequinones

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1,2-Phenanthrenequinone (1,2-PheQ) and 3,4-phenanthrenequinone (3,4-PheQ) were prepared as previously described (Figure 3) (Magdziak et al., 2002 (link)).) [13C4]1,2-PheQ was similarly prepared from [13C4]1-hydroxyphenanthrene ([13C4]1-OHPhe), Cambridge Isotope Laboratories, Inc. (Tewksbury, MA, USA). 1-Hydroxyphenanthrene (1-OHPhe) and 4-hydroxyphenanthrene (4-OHPhe) were obtained from Toronto Research Chemicals (North York, ON, Canada). 9,10-Phenanthrenequinone (9,10-PheQ), benzaldehyde, formic acid, ammonium acetate and sodium acetate were purchased from Millipore Sigma (St. Louis, MO, USA). 8-iso-PGF and [D4]8-iso-PGF were procured from Cayman Chemical (Ann Arbor, MI, USA). β-Glucuronidase and arylsulfatase (from Helix pomatia) were obtained from Roche Diagnostics Corp. (Indianapolis, IN, USA). Oasis® PRiME HLB SPE cartridges (200 mg/6 mL/# 186008057) were from Waters (Milford, MA, USA). A Bond Elut C18 96 square-well plate (100 mg/2 mL/# A396011C) was purchased from Agilent (Santa Clara, CA, USA). All solvents used in this study including hexane, isopropanol, acetonitrile, ethyl acetate and methanol were HPLC grade and obtained from Fisher Scientific (Fair Lawn, NJ, USA). Ultrapure H2O from a Millipore Milli-Q Advantage A10 Water Purification System was used throughout the study.
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8

Hydrogel-based Enzyme Detection System

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Acrylamide (AAm) and N,N′-bis(acryloyl)cystamine (BAC) were purchased from Alfa Aesar. Tetramethylethylenediamine (TEMED) and Amplex UltraRed reagent (AUR) were purchased from ThermoFisher Scientific. Peroxidase from horseradish (HRP), 3-(trimethoxysilyl) propyl methacrylate, dextran from Leuconostoc spp (Mr ~ 100000), and anhydrous (≥99.9%) dimethyl sulfoxide were purchased from Sigma-Aldrich. Ammonium persulfate (APS) was purchased from CalabrioChem Inc. Polyethylene(glycol) diacrylate (PEGDA; Mw = 400) was purchased from PolySciences Inc. Ethanol (EtOH) was purchased from Decon Laboratories Inc. Glacial acetic acid was purchased from Macron Fine Chemicals. Water (dd-H2O) was ionized using Milli-Q Advantage A-10 water purification system (Millipore, U.S.A.). Microscopic glass slides (3” × 1” × 1.2 mm) and micro cover glass (18 mm × 18 mm) were purchased from VWR. Rain-X water repellant manufactured by ITW (Global Bands, TX) was purchased from Home Depot. All UV−vis absorbance spectra were acquired on a Safire2 UV−vis microplate reader (TECAN, Switzerland). The absorbance for the samples were measured at 568 nm in a Nunclon 96-clear Microwell plate. Mechanical characterization tests were performed on a TA Instruments RSA-G2 Solids Analyzer.
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9

Ti–13Zr–13Nb Alloy Surface Preparation

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The material under study was Ti–13Zr–13Nb (wt.%) alloy (BIMO TECH, Wrocław, Poland). Disc-shaped samples with a thickness of 5 mm were cut from a wire with a diameter of 20 mm and a length of 1 m. A specification covering chemical, mechanical and metallurgical requirements for wrought Ti–13Nb–13Zr alloy for surgical implant applications is provided in standard ASTM F1713-08(2021)e1 [41 ]. The samples were subjected to one-sided wet grinding on a metallographic grinding and polishing machine Forcipol 202 (Metkon Instruments Inc., Bursa, Turkey) at 250 rpm of the grinding wheel with soft start and soft stop. SiC abrasive papers of P600, P1200 and P3000 gradations (Buehler Ltd., Lake Bluff, IL, USA) were used. The ground samples with a mirror-like surface were rinsed thoroughly under tap water and sonicated for 20 min in acetone (Avantor Performance Materials Poland S.A., Gliwice, Poland) and then in ultrapure water with resistivity of 18.2 MΩ cm (Milli-Q Advantage A10 Water Purification System, Millipore SAS, Molsheim, France). The cleaning procedure in ultrapure water was repeated twice with a change of water.
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10

Quantitative Analysis of P. aspergillum

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Pierce Quantitative Fluorescent Peptide Assay, Pierce BCA protein assay kit, Page Ruler prestained protein ladder, Pierce C18 Tips, acetonitrile (LC/MS grade) and formic acid (LC/MS grade) were purchased from Thermo Fisher Scientific (Waltham, MA, USA). Protease Inhibitor Cocktail and endoproteinase Glu-C (Sequencing grade) were purchased from Roche (Mannheim, Germany). Phenol solution (pH 7.9 ± 0.2) was purchased from Sangon Biotech (Shanghai, China) Co., Ltd., Genomic. Ultrapure water (18.2 MΩ.cm) was prepared in-house by a Milli-Q Advantage A10 water purification system (Millipore, Bedford, MA, USA). Sequencing-grade modified trypsin and molecular weight cutoff membranes of 10 kDa were purchased from Promega (Promega Corporation, Madison, WI, USA).
P. aspergillum was collected from markets and identified using conventional polymerase chain reaction (PCR) to amplify the cytochrome C oxidase subunit I (COI) gene [35 (link)].
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