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Milli q gradient a 10 water purification system

Manufactured by Merck Group
Sourced in United States

The Milli-Q Gradient A-10 is a water purification system designed to produce high-quality ultrapure water. It uses a combination of filtration, ion exchange, and UV treatment to remove impurities and produce water with low levels of organic and inorganic contaminants. The system is capable of producing water with a resistivity of up to 18.2 MΩ·cm.

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15 protocols using milli q gradient a 10 water purification system

1

Analytical Instrumentation for Metabolomic Research

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The experimental instruments used in this study included the following: Waters ACQUITY UPLC liquid chromatography system, Q-TOF SYNAPT G2 HDMS mass spectrometer, and MassLynx v4.1 chromatographic workstation (Waters, Milford, MA, USA); a high-speed refrigerated centrifuge (Eppendorf, Hamburg, Germany); Vortex Genius 3 vortex oscillator (IKA company, Staufen, Germany); and the Milli-Q Gradient A10 water purification system (Millipore, Billerica, MA, USA).
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2

Caco-2 Permeability of Tenofovir Formulations

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Tenofovir was purchased from Hangzhou Starshine Pharmaceutical Company (Hangzhou, China). Dideoxy-cytosine (ddC) and HPLC-grade dibasic sodium phosphate were purchased from Sigma-Aldrich (St Louis, MO, USA). Hydrogenated phosphatidylcholine (95% hydrogenated phosphatidylcholine and 0.5% hydrogenated lysophosphatidylcholine) was supplied from American Lecithin (Oxford, CT, USA). Cholesterol, stearylamine, phosphoric acid, and HPLC-grade acetonitrile were purchased from VWR (West Chester, PA, USA). Phosphate buffer solution pH 6.8, sodium chloride, sucrose, sodium phosphate, and chloroform were purchased from Fisher Scientific (Pittsburgh, PA, USA). Caco-2 cell line was obtained from American Type Culture Collection (Manassas, VA, USA). Cell culture media and reagents were purchased from Invitrogen Inc. (Carlsbad, CA, USA) and Life Technologies, Inc. (Grand Island, NY, USA). HPLC-ready 18 MW water (deionized [DI] water) was obtained, in-house, from a Milli-Q Gradient A-10 water purification system, Millipore Corporation (Bedford, MA, USA).
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3

Detailed Formulation and Characterization

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CAB 171-15 and C-A-P polymers were obtained from Eastman Chemical Company, Kingsport, TN, USA. DFS were purchased from Leap Chem, Hangzhou, China. Acetone, acetonitrile (ACN), monobasic potassium phosphate, croscarmellose sodium (CCS), magnesium stearate (MGS), polyethylene glycol 400 (PEG, Fisher Scientific, Asheville, NC, USA), hydroxypropyl cellulose (HPC, MW 100,000, Sigma-Aldrich, St Louis, MO, USA), lactose monohydrate (LMH, Supertab 145D, Mutchler Inc, Harrington Park, NJ, USA), and microcrystalline cellulose (MCC, Vivapur® 102, JRS Pharma, Patterson, NY, USA) were used as received. In-house water (18 MΩ.cm, Millipore Milli-Q Gradient A-10 water purification system) was used in the study.
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4

Trace Element Analysis of Biological Samples

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All solutions were prepared with analytical reagent grade chemicals and ultra-pure water (18 MΩ cm) generated by purified distilled water with a Millipore Milli-Q Gradient A-10 water purification system (Bedford, MA, USA). All the plastic and glassware were cleaned by soaking in 2 M HNO3 for 48 h, and rinsed five times with distilled water, and then five times with deionized water prior to use. The calibration standard solutions were freshly prepared by dilution of Optima Family Multi-Element Standard, Matrix per Volume: 2% HNO3 and Multi-Element Calibration Standard 3, Matrix per Volume: 5% HNO3 stock solution (PerkinElmer®, Waltham, MA, USA). A DORM-2 (NRCC, Ottawa, ON, Canada) certified dogfish tissue was used as the calibration verification standard. Recoveries between 90.5 and 108% were accepted to validate the calibration.
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5

Analytical Method Development for Tacrolimus

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TAC monohydrate >98% and hydroxypropyl cellulose (HPC, MW 100,000) were purchased from Sigma-Aldrich (St Louis, MO, USA). Deuterated TAC-13C3D2 (>85%) and Beagle dog plasma were obtained from Toronto Research Chemicals, Ontario, Canada, and BioChemed Services, Winchester, VA, USA, respectively. BioSustane™ SAIB and microcrystalline cellulose (MCC, Avicel® PH-101) were obtained from Eastman Chemical Company (Kingsport, TN, USA) and FMC Corporation (Princeton, NJ, USA), respectively. Hydroxypropyl methylcellulose (HPMC, 50 cps), magnesium stearate (MGS), croscarmellose sodium (CCS), lactose monohydrate, orthophosphoric acid (OPA), methanol, ammonium acetate, zinc sulfate (ZnSO4) and formic acid were purchased from Fisher Scientific (Asheville, NC, USA). Sodium lauryl sulfate (SLS) was purchased from VWR Chemicals, LLC (Fountain Parkway, OH, USA). All reagents were of analytical grade and used as received. In-house water (18 MΩcm, Millipore Milli-Q Gradient A-10 water purification system) was used in the study.
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6

Analytical Reagent Grade Chemicals Protocol

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All solutions were prepared with analytical reagent grade chemicals and ultra-pure water (18 MΩ cm) generated by purified distilled water with a Millipore Milli-Q Gradient A-10 water purification system (Bedford, MA, USA). All the plastic and glassware were cleaned by soaking in 2 M HNO3 for 48 h, and rinsed five times with distilled water, and then five times with deionized water prior to use. The calibration standard solutions were freshly prepared by dilution of Optima Family Multi-Element Standard, Matrix per Volume: 2% HNO3, and Multi-Element Calibration Standard 3, Matrix per Volume: 5% HNO3 stock solution (Perkin Elmer®, Waltham, MA, USA).
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7

Protein Identification via Trypsin Digestion

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Dithiotheritol (DTT), iodoacetamide (IA), ammonium bicarbonate (NH4HCO3) and hydrochloric acid (HCl, 37%) were obtained from Sigma–Aldrich (St. Louis, MO, USA). Formic acid (FA) and acetonitrile (ACN) were purchased from Merck (Darmstadt, Germany). All the reagents used were analytical or HPLC grade. Sequencing grade modified trypsin was from Shanghai Yaxin Biotechnology Co., Ltd (Shanghai, China). All chemical agents were prepared using ultrapure water and without further purification. Ultrapure water was obtained by a Milli-Q Gradient A10 water purification system (Millipore, Bedford, MA, USA) during all the experiments.
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8

Chromatographic Analysis of Amino Acids

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Enrofloxacin (CAS no. 93106-60-6), flumequine (CAS no. 42835-25-6), boric acid (CAS no. 10043-35-3; ≥ 99.8% purity) and phosphoric acid solution (85 wt. % in water) were purchased from Sigma-Aldrich (Steinheim, Germany). DL-Tryptophan (CAS no. 54-12-6; 98% purity), DL-Tyrosine (CAS no. 556-03-6; 99% purity) and 7-amino-4methylcoumarin (coumarin 120, CAS no. 26093-31-2; 98% purity) were from Acros Organics (New Jersey, USA). Glacial acetic acid (CAS no. 64-19-7; HPLC grade) and sodium hydroxide (CAS no. 1310-73-2; pellets) were obtained from Panreac (Barcelona, Spain). Sodium acetate trihydrate (CAS no. 6131-90-4) was from VWR International, LLC (Radnor, Pennsylvania, USA). Ammonium hydroxide (CAS no. 1336-21-6) was obtained from Merck (Darmstad, Germany).
Deionised water was obtained by using the Milli-Q gradient A10 water purification system from Millipore (Bedford, MA, USA).
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9

Sildenafil Citrate Formulation and Validation

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A pharmaceutical grade of sildenafil citrate (Matrix Laboratories Mumbai-India) was used in all formulations produced while a purity grade of sildenafil (Purity Grade Standards, 99.8% content, USA, Lot: 1110-026A1) was used for the validation of all analyses in this study. Sodium metabisulfite, propylene glycol and sodium saccharin were obtained from Vetec (Vetec Chemical, RJ, Brazil), Span® 20, Span® 80 and Tween® 80 were obtained from Sigma (Sigma Chemical Co., St. Louis, MO, USA). Isobutanol was purchased from Tedia (Tedia Company Inc, Ohio, USA) and 2-pyrrolidone (Soluphor P®) from BASF (São Paulo, SP, Brazil). Both of these compounds were of pharmaceutical grade. Syringe filters had a pore size of 0.45 μm and cellulose acetate synthetic membranes were purchased from Millipore (Bedford, MA, USA). The water used in this study was obtained using a Milli-Q Gradient A-10 water purification system, Millipore, (Bedford, MA, USA). All other chemicals utilized were either analytical or HPLC grade.
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10

Proteomic Sample Preparation Reagents

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Ammonium bicarbonate (NH4HCO3), dithiothreitol (DTT), iodoacetamide (IA) and hydrochloric acid (HCl, 37%) were obtained from Sigma-Aldrich (St. Louis, MO, USA). Acetonitrile (ACN) and formic acid (FA) were purchased from Merck (Darmstadt, Germany). All the reagents used were analytical or HPLC grade. Sequencing grade modified trypsin was from Shanghai Yaxin Biotechnology Co., Ltd (Shanghai, China). All chemical agents were prepared using ultrapure water and without further purification. Ultrapure water was obtained by a Milli-Q Gradient A10 water purification system (Millipore, Bedford, MA, USA) during all the experiments.
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