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57 protocols using cesium chloride

1

Synthesis and Characterization of Perovskite Nanoparticles

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Oleic acid (OAc, 90%, Sigma-Aldrich), n-octylamine (99.0%, Aladdin), N,N-dimethyl-formamide (DMF, 99.9%, Aladdin), cyclohexane (99.0%, Aladdin), methyl acetate (99.9%, Aladdin), n-Hexane (99.0%, Aladdin), styrene (99.9%, Aladdin), cesium bromide (CsBr, 99.9%, Sigma-Aldrich), cesium chloride (CsCl, 99.9%, Sigma-Aldrich), lead(II) bromide (PbBr2, 99.9%, Sigma-Aldrich), and zirconium (IV) chloride (ZrCl4, 99.9%, Sigma-Aldrich). All chemical reagents are used as received.
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2

Extraction and Utilization of Moroccan Phosphate

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Phosphate samples used in this study come from an extracted ore of Khouribga deposits, an important source of phosphate in Moroccan kingdom. Cesium chloride (CsCl) was purchased from Sigma Aldrich, rapeseed oil was purchased from a local company in Mohammedia city, Morocco and was directly used without further treatment. Waste cooking oil (WCO) was supplied by a local restaurant and was filtered before being used in the transesterification experiment to eliminate solid suspensions. All chemicals were analytical grade and were directly used without any further purification.
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3

Purification of Murine Viral Warts

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Muzzle warts of B6.Cg-Foxn1nu/Foxn1nu mice were
homogenized via pulverization with a mortar and pestle in liquid nitrogen then
homogenized with a tissue grinder (DWK Life Sciences, Millville, New Jersey,
catalogue no. 885450–0023). Tissue was then subjected to three
freeze-thaw cycles between liquid nitrogen and a 37˚C water bath. Tissue
was then sonicated for two minutes (amplitude = 20, 10s pulse). Cesium Chloride
(Sigma-Aldrich, St. Louis, MO, catalogue no. 289329) dissolved in
phosphate-buffered saline (PBS) was added to the wart homogenate for a final
density of 1.3623 g/mL, determined via refractometer (product discontinued).
Tissue was ultracentrifuged overnight at 36,000 rpm and opaque bands at
densities ranging from 1.27–1.31 g/mL were extracted. Extracted bands
were dialyzed three times for eight hours using Slide-A-Lyzer cassette (VWR,
catalogue no. PI66230) in three liters of PBS. The purity of the viral
preparation was confirmed using SDS-PAGE gel electrophoresis.
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4

Perovskite Precursor Synthesis

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Cesium bromide (CsBr, 99.9%) is purchased
from Alfa Aesar, and lead bromide (PbBr2, 98%), cesium
chloride (CsCl, 99.999%), polyethylene oxide (PEO, Mw ≈ 600,000),
and dimethylsulfoxide (DMSO, anhydrous) are purchased from Sigma Aldrich.
Lead chloride (99.999%) is purchased from Lumtec. Poly(3,4-ethylenedioxythiophene)
polystyrene sulfonate (PEDOT:PSS, AI 4083) is purchased from Clevios.
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5

Extraction and Analysis of Mangrove Phytochemicals

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Water used in this experiment was purified on a Millipore Milli-Q apparatus. HPLC grade dichloromethane, acetonitrile (CH3CN), methanol, trifluoroacetic acid (TFA), acetic acid, and all analytical grade solvents (acetone, methanol, n-Butanol etc.) were obtained from Sinopharm (Sinopharm, Shanghai, China). Sephadex LH-20, Folin-Ciocalteu reagents, acetone-d6, deuteroxide (D2O), Amberlite IRP-64 cation-exchange resin, cesium chloride (CsCl), 2,5-dihydroxybenzoic acid (DHB), benzylmercaptan, 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,4,6-tripyridyl-S-triazine (TPTZ), ascorbic acid (AA), and all HPLC standards were purchased from Sigma (St. Louis, MO, USA). The mature leaves (the third pair with fully expanded and dark green) of a mangrove plant C. tagal (Rhizophoraceae Ceriops), were collected from a mangrove forest in the Dongzhai harbor (19°56′N, 110°34′E), Hainan, China. The leaves were immediately freeze-dried, ground, and stored at −20°C prior to analysis.
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6

Metabolic Regulation of Cell Cycle and Oxidative Stress

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Gelatin, sodium dodecyl sulfate (SDS), dithiothreitol, NaCl, EDTA, heparin, trichloroacetic acid, trypan blue, propidium iodide, RNase, cesium chloride, M199 medium, dimethyl-α-ketoglutarate, aspartate, hydrogen peroxide, glutamine, dialyzed fetal bovine serum, trypsin, 6-diazo-5-oxo-L-norleucine (DON), mercaptoethanol, streptomycin, penicillin, bis-2-(5-phenylacetomido-1,3,4-thiadiazol-2-yl)ethyl sulfide (BPTES), glutamate, ammonium chloride, and diethylamine NONOate (DEA-NO), K2HPO4, ATP, NAD, hydrazine, bovine liver glutamate dehydrogenase, and asparagine were from Sigma-Aldrich (St. Louis, MO). Endothelial cell growth factor was from Becton Dickinson Biosciences (Bedford, MA). Rainbow molecular weight markers were from GE Healthcare (Piscataway, NJ). Lipofectamine and 5-(and-6)-chloromethyl-2,7-dichlorodihydrofluorescein diacetate acetyl ester (CM-H2DCFDA) were from Life Technologies Corporation (Carlsbad, CA). CB-839 and NG-nitro-L-arginine methyl ester (L-NAME), were from Selleckchem (Houston, TX). Antibodies against GLS1, cyclin D1, cyclin E, cyclin A, p21, p27, p53, and β-actin were from Santa Cruz Biotechnology (Santa Cruz, CA), an antibody against phospho-retinoblastoma protein was from Cell Signaling Technologies (Beverley, MA), and an antibody against HO-1 was from Assay Designs (Ann Arbor, MI). [3H]Thymidine (20 Ci/mmol) was from Perkin Elmer (Boston, MA).
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7

Synthesis of Perovskite Thin Films

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Lead(II) bromide (PbBr2, 99.999% trace metals basis); cesium bromide (CsBr, 99.999% trace metals basis); lead(II) chloride (PbCl2, 99.999% trace metals basis); cesium chloride (CsCl, 99.999% trace metals basis) and polymethyl methacrylate (Mw = 120,000 g/mol) (PMMA) were purchased from Sigma-Aldrich (Saint Louis, MO, USA). All chemicals were used as received, without further purification.
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8

Phage Concentration and Purification

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Individual phages (Table 1) were propagated as described above in a 2 L volume before the addition of (poly)ethylene glycol (Sigma-Aldrich) to a final volume of 10% (w/v) and NaCl (Sigma-Aldrich) to a final concentration of 0.5 M. The mixtures were incubated at 4°C for at least 6 h to encourage precipitation before centrifugation at 17,700 × g for 15 min (to concentrate) and resuspension in 5 ml TBT Buffer (100 mM NaCl, 100 mM Tris-HCl (pH 7), 10 mM MgCl2, 20 mM CaCl2; Sigma-Aldrich). The suspension was extracted at least twice using an equal volume of chloroform (Fisher Scientific, Waltham, MA, U.S.A.) and phages were purified by a discontinuous (3 M/5 M) cesium chloride (Sigma-Aldrich) gradient centrifugation at 76,000 × g for 2.5 h. Translucent blue bands visible at the interface of the gradient after centrifugation were carefully removed using a syringe and dialyzed against 50 ml TBT overnight at 4°C. Phage preparations were stored at 4°C until required for electron microscopy and DNA extraction.
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9

Purification of Murine Viral Warts

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Muzzle warts of B6.Cg-Foxn1nu/Foxn1nu mice were
homogenized via pulverization with a mortar and pestle in liquid nitrogen then
homogenized with a tissue grinder (DWK Life Sciences, Millville, New Jersey,
catalogue no. 885450–0023). Tissue was then subjected to three
freeze-thaw cycles between liquid nitrogen and a 37˚C water bath. Tissue
was then sonicated for two minutes (amplitude = 20, 10s pulse). Cesium Chloride
(Sigma-Aldrich, St. Louis, MO, catalogue no. 289329) dissolved in
phosphate-buffered saline (PBS) was added to the wart homogenate for a final
density of 1.3623 g/mL, determined via refractometer (product discontinued).
Tissue was ultracentrifuged overnight at 36,000 rpm and opaque bands at
densities ranging from 1.27–1.31 g/mL were extracted. Extracted bands
were dialyzed three times for eight hours using Slide-A-Lyzer cassette (VWR,
catalogue no. PI66230) in three liters of PBS. The purity of the viral
preparation was confirmed using SDS-PAGE gel electrophoresis.
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10

Ion Channel Modulation Assay

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Nifedipine, NA, tetraethylammonium chloride (TEA), ACH, pyrazole-3 (Pyr3), bovine serum albumin (BSA), papain, collagenase H, dithiothreitol (DTT), dithioerythritol (DTE), cesium acetate, cesium chloride (CsCl), Mg-ATP, and agarose were purchased from Sigma (St. Louis, MO, USA). Nifedipine and Pyr3 were dissolved in dimethyl sulfoxide (DMSO), and other compounds were dissolved in the appropriate solutions used in the experiments.
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