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38 protocols using sodium chloride (nacl)

1

Activated Carbon-based Membrane Fabrication

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Activated carbon (AC, MSP-20X) was purchased from Kansai Coke & Chemicals Co. (Hyogo, Kobe, Japan). Cationic- and anionic-exchange membranes were obtained from Fujifilm (Type 10, Tilburg, The Netherlands). Deionized water was produced using the Human Power II+ purification system (Human Corporation, Seoul, Korea). Multi-wall carbon nanotubes (CNTs) were obtained from Cheap Tubes Inc. (Grafton, VT, USA). Poly (vinylidene fluoride) (PVDF, Mw ~534,000 g/mol), Polyvinylpyrrolidone (PVP, Mw ~40,000 g/mol), and N-Methyl-2-pyrrolidone (NMP) were purchased from Sigma-Aldrich Inc. (St. Louis, MI, USA). Sodium chloride (99.5%) and methanol (99.9%) were purchased from Samchun Chemicals Co. (Seoul, Korea). 2-Methylimidazole (C4H6N2, 99%) and Cobalt (II) nitrate hexahydrate (Co(NO3)2·6H2O, 97.7%) were obtained from Thermo Fisher Scientific Co. (Ward Hill, MA, USA). All the chemicals were of analytical grade and were used as received from the suppliers without further purification.
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2

Calcium and Glucose Signaling in Cells

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Potassium chloride (KCl) and sodium chloride (NaCl) were purchased from Samchun Chemical (Seoul, South Korea). Calcium chloride (CaCl2), magnesium chloride (MgCl2), 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), and alpha-D-glucose were supplied by Sigma-Aldrich (Saint Louis, MO). Fetal bovine serum was obtained from Lonza (Walkersville, MD), and penicillin-streptomycin was purchased from Gibco (Carlsbad, CA). Fura-2 acetoxymethyl ester (fura-2/AM) was obtained from Invitrogen (F-1225; Eugene, OR). RPMI 1640 was purchased from Welgene (Seoul, South Korea). Collagenase P (from Clostridium histolyticum; 11213865001) was obtained from Roche Diagnostics (Indianapolis, IN). All of the solutions were prepared using Milli-Q deionized water (Millipore, 18.2 MΩ/cm at 25°C). All of the buffer solutions used in the experiments contained 125 mM NaCl, 5.9 mM KCl, 2.56 mM CaCl2, 1.2 mM MgCl2, 25 mM HEPES (pH 7.4), and various concentrations of glucose (3–15 mM as indicated). The buffer was supplemented with 1 mg/mL BSA (fraction V; USB 10857; Cleveland, OH).
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3

Urea-Based Agar Media Preparation

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urea base (0.5 g peptone (Sigma-Aldrich), 0.5 g dextrose (Sigma-Aldrich), 2.5 g sodium chloride (Samchun Chemicals Co. Ltd., Seoul, Korea), 1 g potassium phosphate monobasic (Sigma-Aldrich), and 10 g urea (Sigma-Aldrich)) was dissolved in 50 mL of DI water, and the resulting mixture was filtered using a syringe filter (0.45 μm, Whatman, Maidstone, UK). Additionally, a mass of 10 g of agar (BD, Franklin Lakes, NJ, USA) was dissolved in 450 mL of DI water, and the resulting solution was autoclaved (MDM-60ST, MDM, Suwon-si, Gyeonggi-do, Korea) at 121 °C for 15 min and then allowed to cool down to 50–55 °C. At this point, the urea base solution was added to the agar solution and this composition was gently mixed. Six milliliters (6 mL) of the resulting liquid mixture were added into respective 20-mL glass vials and, at ambient temperature, allowed to solidify for 40 min. The vials were then closed using screw caps and stored at 4 °C prior to use.
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4

Preparation of Simulated Gastrointestinal and Plasma Fluids

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Simulated gastric, intestinal, and plasma fluids were prepared for in vitro studies as previously described [50 ]. The simulated gastric fluid was prepared by dissolving 2 g sodium chloride (Samchun Chemical Co., Ltd., Pyeongtaek, Korea) and 3.2 g pepsin (Sigma-Aldrich, St Louis, MO, USA) in DW, and the pH was adjusted to 1.5 with 1 N hydrochloric acid (Duksan Pure Chemicals Co., Ltd., Ansan, Gyeonggi-do, Korea), and then made up to 1000 mL. For the simulated intestinal fluid, bile salt (87.5 mg) (Sigma-Aldrich, St Louis, MO, USA) and pancreatin (25 mg) (Sigma-Aldrich, St Louis, MO, USA) were added to the simulated gastric fluid, and then the pH was adjusted to 6.8 with saturated sodium bicarbonate solution (Sigma-Aldrich, St Louis, MO, USA). The simulated plasma fluid was prepared by dissolving 50 g of BSA (Sigma-Aldrich, St Louis, MO, USA) in PBS solution (NaCl 137 mM, KCl 2.7 mM, Na2HPO4 10 mM, KH2PO4 1.8 mM; Dongin Biotech. Co., Ltd., Seoul, Korea), and then made up to 1000 mL.
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5

MRSA Cultivation and Storage Protocol

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MRSA CCARM 3807 [61 (link)] and CCARM 3820 were purchased from the Culture Collection of Antimicrobial Resistance Microbes at Seoul Women’s University (Seoul, Republic of Korea). The strains were stored in 25% glycerol (catalog number: 4066-4400, Daejung Chemical & Metals Co., Ltd., Siheung, Republic of Korea) at −80 °C.
Both strains were cultured in Tryptic Soy Broth (TSB, catalog number: 211825, Becton Dickinson Korea Co., Ltd., Seoul, Republic of Korea) and plated on Tryptic Soy Agar (TSA) plates made by adding 1.5% Bacto-Agar (catalog number: 214010, Becton Dickinson Korea) to TSB.
Saline was prepared by adding 0.85% (w/v) of sodium chloride (catalog number: S0476, Samchun Chemicals Co., Ltd., Seoul, Republic of Korea) to distilled water. All solutions were sterilized at 121 °C for 20 min. The strains were cultured at 37 °C with a shaking speed of 250 rpm for liquid cultures.
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6

Quantitative Analysis of Paclitaxel and Metabolites

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Paclitaxel (PTX), 3′-p-hydroxypaclitaxel (3p-OHP), and 6αhydroxypaclitaxel (6α-OHP) were purchased from BD Biosciences (San Diego, CA, USA) and used without further purification. Lithium chloride and sodium chloride were purchased from Samchun Pure Chemical (Pyeongtaek, Korea). Potassium chloride from Junsei Chemical (Tokyo, Japan) and silver nitrate from Tokyo Chemical Industry (Tokyo, Japan) were used. HPLC-grade water, ethanol, (J. T. Baker, Phillipsburg, NJ, USA) and formic acid (Sigma-Aldrich, St. Louis, MO, USA) were used. Polyalanine was purchased from Sigma-Aldrich. The final concentration of the analyte (PTX, 3p-OHP, and 6α-OHP) was adjusted to 5 μM. Except for silver nitrate, all the other metal salts were added to be equimolar with the analyte. Silver nitrate concentration was selected to be 10-fold of paclitaxel and its metabolites to obtain observable signal of complex. All sample solutions were prepared in 50/50 water/ethanol with 0.5% of formic acid by volume.
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7

Donepezil Hydrochloride Formulation Development

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Donepezil hydrochloride was purchased from Sinoway Industrial Co., Ltd. (Xiamen, China). Donepezil-D7 was obtained from Toronto Research Chemicals Inc. (Toronto, ON, Canada). Aricept® 5 mg was from Daewoong Pharmaceutical Co., Ltd. (Seoul, Korea). Hydroxypropyl methylcellulose (HPMC) 2208–100 cps and HPMC 2208–4000 cps were purchased from Shin-Etsu Chemical Co., Ltd. (Tokyo, Japan). Lactose and magnesium stearate were purchased from Whawon Pharm. Co., Ltd. (Seoul, Korea) and Faci Asia Pacific Pte Ltd. (Jurong Island, Singapore), respectively. Acetic acid and formic acid were obtained from Sigma-Aldrich Co. (St. Louis, MO, USA). Hydrochloric acid, potassium dihydrogen phosphate, and ethanol were obtained from Merck Co. (Darmstadt, Germany). Sodium hydroxide and sodium chloride were purchased from Samchun Chemical Co., Ltd. (Seoul, Korea). HPLC-grade acetonitrile and water were purchased from J.T. Baker Co. (Philipsburg, NJ, USA).
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8

Corrosion Inhibition of AA 2024-T3 Alloy

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Tetraethylenepentamine (TEPA, technical grade), cerium (III) chloride heptahydrate (CeCl3. 7H2O, 98%), and carbon disulphide (CS2, 99.9%) were purchased from Sigma-Aldrich Co., Ltd., Seoul, Korea. Sodium chloride (NaCl, 99.5%) and sodium hydroxide (NaOH, 98%) were provided by Samchun Chemical Co., Ltd., Seoul, Korea. Ethanol (EtOH), acetone, acetonitrile, and AA 2024-T3 alloy were purchased from local Korean companies. The chemical composition of the AA 2024-T3 alloy used was 0.45% Si, 0.45% Fe, 0.46% Mn, 1.2–1.8% Mg, and 3.8–4.9% Cu, with the remaining balance being Al.
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9

Synthetic Brine and Real BWRO Brine Comparison

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A synthetic brine of seawater reverse osmosis (SWRO) was used as the high-salinity (HS) solution, which was prepared using sodium chloride (Samchun, Seoul, Korea) and deionized water. The NaCl concentration of the HS solution was 1.0 M. A real BWRO brine from a wastewater reclamation plant was used as the low-salinity (LS) solution. The feed water to the BWRO process was the effluent of a municipal wastewater treatment plant.
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10

Leaf Senescence Assay Protocol

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The third and fourth leaves of 3-week-old plants were harvested and floated on 3 mM MES (pH 5.7). The samples were incubated at 22 °C in the dark for up to 11 d. The photochemical efficiency of PSII (Lee et al., 2016 (link)) and chlorophyll content (Vernon, 1960 ) of leaves were measured as described previously. For chemical- or plant hormone-mediated senescence assay, detached leaves were floated abaxial side up in 3 mM MES (pH 5.7) with or without 50 μM 1-aminocyclopropane-1-carboxylic acid (ACC; Sigma, USA), 0.2 μM 6-benzylaminopurine (BA; Sigma, USA), 100 mM sodium chloride (Samchun, Korea), or 10 mM hydrogen peroxide (Junsei, Japan). All treatments were performed at 22 °C in the dark. Photochemical efficiency and chlorophyll content were measured as described above. For developmental leaf senescence assays, the third and fourth rosette leaves at the indicated leaf age were harvested from individual plants and used for measurements of chlorophyll content, photochemical efficiency, and gene expression. Leaves used for gene expression and microarray experiments were harvested 4 h into the subjective day.
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