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Sodium phosphate monohydrate

Manufactured by Merck Group
Sourced in United States, Poland

Sodium phosphate monohydrate is a chemical compound used as a laboratory reagent. It is a white, crystalline solid that is soluble in water. The compound's primary function is to provide a source of phosphate ions for various chemical and biochemical applications.

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5 protocols using sodium phosphate monohydrate

1

Chitosan-Based Enzyme Inhibition Assay

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Chitosan (medium molecular weight), sodium hydroxide, citric acid, sodium phosphate monohydrate and rat intestinal acetone powder and 4-nitrophenyl-α-D-glucopyranoside (pNPG) were purchased from Sigma-Aldrich (St. Louis, Mo., U.S.A.). 3% glutaraldehyde was obtained from Ricca Chemical Co. (Arlington, TX, U.S.A.). Acarbose was purchased from LKT, Inc. (St. Paul, MN, U.S.A.).
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2

Tryptic Digest of Reduced BSA

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D2O (99.96 mol %
D) was acquired from Cambridge Isotopes (Andover, MA). Sodium phosphate
dihydrate, sodium phosphate monohydrate, sodium chloride, and formic
acid (FA) were purchased from Sigma-Aldrich (St. Louis, MO). Ethylene
glycol ReagentPlus (>99%) was purchased from Alfa Aesar (Ward Hill,
MA). The analytical sample used for these experiments was a tryptic
digest of fully reduced and iodoacetamide alkylated BSA (Thermo Scientific
Pierce BSA Protein Digest Standard, LC–MS grade, catalog no.
88341).
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3

Amyloid-beta Peptide Synthesis

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Lyophilized Aβ1–42 and Aβ1–16 peptide were purchased from rPeptide (Watkinsville, GA, USA). Bovine insulin, DEPC; 1,1,1,3,3,3‐hexafluoro‐2‐propanol (HFIP); sodium chloride; sodium hydroxide; ammonium hydroxide; sodium phosphate monohydrate; disodium phosphate heptahydrate; α‐cyano‐4‐hydroxycinnamic acid (α‐CHCA); acetonitrile; trifluoroacetic acid; thioflavin T (ThT); and hydroxylamine hydrochloride (NH2OH·HCl) were purchased from Sigma‐Aldrich (St. Louis, MO, USA).
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4

Phosphate Binding Efficiency of Liposomes

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To test the liposomes’ ability to trap free phosphate ions in solution, liposomes were incubated with phosphate solutions at increasing concentrations. To this end, phosphate solutions were prepared by a series of dilutions of sodium phosphate monohydrate (Sigma-Aldrich) dissolved in HEPES-buffered saline (10 mM HEPES, 150 mM NaCl, pH = 7.4) to yield solutions with increasing phosphate concentrations of 0.625, 1.25, 2.5, 5, 10, 20, 40, and 60 mg/dL. A dialysis tube with 1 mL FC liposomes (1.22 mg FC) was placed in 70 mL of each phosphate solution, or in HEPES with no phosphate, for 24 h at 37 °C under constant stirring. Elemental analysis of phosphorus in each solution before and after incubation with the liposomes was performed by ICP-OES. Phosphate binding efficiency was calculated by the following formula: P t0 mgdLP t24mgdL· PO43Mw grmolP Mw grmo=[PO4]3 bindingmgml FC LP
Equation (1). Calculation of phosphate binding efficiency (P: phosphorus, PO4−3: phosphate, t24: post 24 h of incubation with liposomes, FC LP: FC liposomes).
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5

Quantum Dots for Neurotransmitter Detection

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Oleic acid-capped quantum dots (QDs-OA) with alloyed (CdSexS1-x) core and ZnS shell (CdSeS/ZnS), nanocrystal diameter = 6.0 nm, λem = 630 nm, 1 mg/mL in toluene were purchased from Cytodiagnostics Inc. (Burlington, Canada). Glutathione in reduced form (GSH) was from Acros Organics (Geel, Belgium). Tetramethylammonium hydroxide pentahydrate (TMAH) was from Alfa Aesar (Kandel, Germany). Chloroform, anhydrous ethanol, and phosphoric acid (85%) were obtained from Chempur (Piekary Śląskie, Poland). Dialysis tubing cellulose membrane (MWCO = 12 kDa), dopamine hydrochloride, L-epinephrine, L-norepinephrine, serotonin hydrochloride, γ-aminobutyric acid (GABA), acetylcholine chloride, sodium phosphate monohydrate, disodium phosphate dodecahydrate, and sodium hydroxide were supplied by Sigma-Merck (Poznań, Poland). Milli-Q water was used for preparation of all aqueous solutions. All chemicals were used as received.
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