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).
Fisher optima lc ms grade water
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.
3 protocols using fisher optima lc ms grade water
Quantitative Analysis of Vitamin D Metabolites
Amyloid-β Peptide Binding Assay
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.
Quantification of Aβ42 Oligomers using Mass Spectrometry
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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