Millipore milli q system
The Millipore Milli-Q system is a water purification system designed to produce high-quality, ultrapure water for laboratory applications. It employs a multi-stage purification process to remove various contaminants, including organic compounds, ions, and microorganisms, from the input water source.
Lab products found in correlation
55 protocols using millipore milli q system
Resorcinol Permeation Assay Protocol
Sodium Alginate-Based Biomaterial Synthesis
Electrochemical Activation of Screen-Printed Gold Electrodes
Before the start of a biosensing experiment, the SPE was mounted in the 3D-printed static cell with the top part enclosing all electrodes, cleaned, and activated according to the procedure described and optimized by Henihan et al. [49 (link)]. In brief, 100 µL of 0.1 mol L−1 sulfuric acid (H2SO4) was applied on all electrodes of the SPE. Then, 10 electrochemical cyclic voltammetry (CV) cycles with a voltage between 0 and 1.6 V, followed by three CV cycles with a voltage between 0 and 1.3 V, were run. After a biosensing experiment was done, the SPE was washed thoroughly with deionized nuclease-free water (Millipore Milli-Q® system, Merck KGaA, Darmstadt, Germany) and cleaned with the same CV procedure.
Cultivation of Plant In Vitro Cultures
Ultrapure water was obtained using Millipore Milli-Q system (Merck Millipore, Molsheim, France). Acetonitrile and methanol were purchased from Thermo Fisher Scientific (Illkirch-Graffenstaden, France). Standard compounds L-leucine, L-isoleucine, L-phenylalanine, L-tyrosine, L-tryptophan, L-proline, citric acid, gallic acid, coutaric acid, trans-resveratrol, cis-resveratrol, E-piceid, catechin, epicatechin, catechin gallate, tyrosinase, and L-DOPA were purchased from Sigma-Aldrich (St. Louis, MO, USA). Rhamnetin, E-ε-viniferin, quercetin 3-O-glucoside, quercetin 3-O-glucuronide, quercetin-3-O-galactoside, procyanidin B1, procyanidin B2, procyanidin B3, and procyanidin C1 were obtained from ExtraSynthèse (Genay, France); caftaric acid was delivered by Carbosynth (Compton, Berkshire, UK), while E-ε-viniferin, Z/E-vitisin B, ampelopsin A, and hopeaphenol were obtained by previous extraction from grape stems [50 (link)].
Cultivation of Plant In Vitro Cultures
Ultrapure water was obtained using Millipore Milli-Q system (Merck Millipore, Molsheim, France). Acetonitrile and methanol were purchased from Thermo Fisher Scientific (Illkirch-Graffenstaden, France). Standard compounds L-leucine, L-isoleucine, L-phenylalanine, L-tyrosine, L-tryptophan, L-proline, citric acid, gallic acid, coutaric acid, trans-resveratrol, cis-resveratrol, E-piceid, catechin, epicatechin, catechin gallate, tyrosinase, and L-DOPA were purchased from Sigma-Aldrich (St. Louis, MO, USA). Rhamnetin, E-ε-viniferin, quercetin 3-O-glucoside, quercetin 3-O-glucuronide, quercetin-3-O-galactoside, procyanidin B1, procyanidin B2, procyanidin B3, and procyanidin C1 were obtained from ExtraSynthèse (Genay, France); caftaric acid was delivered by Carbosynth (Compton, Berkshire, UK), while E-ε-viniferin, Z/E-vitisin B, ampelopsin A, and hopeaphenol were obtained by previous extraction from grape stems [50 (link)].
Preparation of Defined Buffer Solutions
Characterization of Phenolic Compounds
Comprehensive Phytochemical Characterization
Raphanus sativus L. Seed Extraction
Antioxidant Potential of Grape Phenolics
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