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Fisher optima lc ms grade water

Manufactured by Thermo Fisher Scientific

Fisher Optima LC-MS grade water is a highly-purified, laboratory-grade water specifically designed for use in liquid chromatography-mass spectrometry (LC-MS) applications. It is produced to meet the stringent purity requirements of LC-MS instrumentation and analysis.

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3 protocols using fisher optima lc ms grade water

1

Quantitative Analysis of Vitamin D Metabolites

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25-hydroxyvitamin D3, D6-25-hydroxyvitamin D3, and 3-epi-25-hydroxyvitamin D3 standards (100 μg/mL in ethanol) were purchased from IsoSciences (King of Prussia, PA). These standards were diluted to a final concentration of 10 μg/mL in Fisher Optima LC-MS grade water, purchased from Fisher Scientific (Pittsburgh, PA), with no additives.
Lithium acetate, magnesium acetate tetrahydrate, and calcium acetate monohydrate were purchased from Acros Organics (Geel, Belgium). Potassium acetate was purchased from Alfa Aesar (Haverhill, MA). Rubidium acetate was purchased from Strem Chemicals (Newburyport, MA). Cesium acetate was purchased from MP Biomedicals (Santa Ana, CA). Strontium acetate was purchased from Sigma-Aldrich (St. Louis, MO). Barium acetate was purchased from Chem-Impex International, Inc. (Wood Dale, IL). These standards were combined with the aforementioned vitamin D standards and were diluted to a final concentration of 10 μg/mL in Fisher Optima LC-MS grade methanol or a 1:1 mixture of Fisher Optima LC-MS grade water and methanol, depending on their relative solubility. Flame emission testing was used to estimate the sodium concentration in the solvents as approximately 185 ppb (water) and 220 ppb (methanol).
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2

Amyloid-β Peptide Binding Assay

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Data for Aβ42 peptide were acquired using a Waters Synapt G2-S Q-TOF MS with traveling wave ion mobility (Waters Corp.). The data were acquired using the systems sensitivity mode to allow for the detection of the less abundant oligomers. Samples were infused at room temperature, as described.
3-SPA (1 mg) was reconstituted in 1 ml of Fisher Optima LC–MS grade water (cat# W6-1) and vortexed vigorously for 2 min until completely dissolved. The sample was then diluted to create 220 and 22,000 pmol/µl solutions to perform a 100-fold and 1000-fold molar excess for the binding experiments with Aβ42 peptide.
Recombinant human Aβ42 peptide (1 mg) was reconstituted in 200 µl of Fisher Optima LC–MS grade water and vortexed vigorously to solubilize to a 5 mg/ml solution. Samples were then diluted to their final concentrations and incubated at room temperature for 0, 4, and 24 h, followed by analysis, as described.
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3

Quantification of Aβ42 Oligomers using Mass Spectrometry

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The data acquisition for Aβ42 peptide was performed using a Waters Synapt G2-S Q-TOF MS with traveling wave ion mobility (Waters Corp.). The data were acquired using the systems sensitivity mode to allow for the detection of the less abundant oligomers. Samples were infused at room temperature as in the previous section.
We reconstituted 1 mg of tramiprosate in 1 ml of Fisher Optima LC/MS grade water (cat# W6-1) and vortexed it vigorously for 2 min until completely dissolved. The sample was then diluted to create 220, 2200, and 22,000 pmol/µl solutions to perform a 10-, 100-, and 1000-fold molar excess for the binding experiments with Aβ42.
We reconstituted 1 mg of recombinant human Aβ42 peptide in 200 µl of Fisher Optima LC/MS grade water and vortexed vigorously to solubilize to a 5 mg/ml solution. Samples were then diluted to their final concentrations prior to incubation. The sample mixtures were incubated at room temperature for 0, 4, and 24 h, followed by analysis as described in the previous subsections.
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