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Barium chloride bacl2

Manufactured by Merck Group
Sourced in United States

Barium chloride (BaCl2) is an inorganic compound that is commonly used as a laboratory reagent. It is a white, crystalline solid that is soluble in water. Barium chloride is primarily used as a precipitating agent for the detection and determination of sulfate ions in analytical chemistry.

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10 protocols using barium chloride bacl2

1

Fluorocitric Acid Preparation and Use

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DL-fluorocitric acid (FCA) barium salt (#F9634) and barium chloride (BaCl2, #217565) were purchased from Sigma-Aldrich. Because FCA was commercially available as Ba2+ salt, which may interfere with neuronal physiological properties leading to confounding results, we decided (Chou et al., 2009 (link)) to use BaCl2 salt in control patch-clamp experiments and (Furlan et al., 2006 (link)) to precipitate Ba2+ during drug preparation for in vivo stereotaxic microinjections. For electrophysiology experiments (see 2.6), BaCl2 was dissolved in H2O and FCA in HCl 0.1 M as a stock solutions and diluted (1:100) to the final concentration (100 µM) in artificial cerebrospinal fluid (ACSF, in mM: 117 NaCl, 4.7 KCl, 1.2 NaH2PO4, 2.5 CaCl2, 1.2 MgCl2, 25 NaHCO3 and 11 glucose) on the day of the experiment (Khan et al., 2019 (link); Vizuete et al., 2019 (link)). For intra-CeA microinjection (see 2.7.1), the compound was dissolved in HCl 0.1 M and the Ba2+ was precipitated by the addition of (2–3 drops) Na2SO4 0.1 M. This solution was buffered with Na2HPO4 0.1 M and centrifuged at 800 g for 10 min. The supernatant was removed and diluted in ACSF to the final concentration (100 µM) and pH was adjusted to 7.3 (Paulsen et al., 1987 (link); Hayakawa et al., 2010 (link); Paquette et al., 2021 (link)).
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2

Hydrogel-Coated Mini-Pillars for 3D Cell Culture

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The mini-pillars were custom-made by MBD Co. (Cat. No. Cellvitro™ 55Cryo, 873087@mbdker.co.kr). Mini-pillar inserts with 2 mm diameter were made with polystyrene by injection molding. The pillars were inserted in 9 mm-pitch holes on the pillar holder for cell culture in 96-well plates (Fig. 1A) and in 3.2 mm-pitch holes for cryosection (Fig. 1B). The mini-pillars were sterilized before pre-coating and cell loading by boiling in 70% ethanol for 30 min followed by UV irradiation as described previously.34 (link) Poly-l-lysine (PLL) pre-coating was used to stabilize the loading of hydrogel (alginate, collagen, or Matrigel) onto the tip of the mini-pillar.34 (link) When using alginate as hydrogel, the pillar tip was subjected to barium coating for cell loading: 2 μL of 100 mM barium chloride (BaCl2, Sigma-Aldrich) was dispensed on the surface of the pillar and dried in a biosafety cabinet for 3 h. BaCl2 was used as a cross-linking agent for the alginate hydrogel since barium ion chelates with carboxylic groups on alginate.
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3

Multiparametric Analysis of Cell Viability

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Sodium oleate (Sigma-Aldrich, Cat# O7501), AlexaFluor568 protein labeling kit (Thermo Scientific, Cat# A10238), AlexaFluor488 protein labeling kit (Thermo Scientific, Cat# A10235), ATPlite (Perkin Elmer, Cat# 6016947), Presto Blue Cell Viability Assay (Invitrogen, Cat# A13262), Anti-peptide antibodies (this study, produced by GeneCust), FluxOR Potassium ion channel assay (Invitrogen, Cat# F20015), Barium chloride BaCl2 (Sigma-Aldrich, Cat# B0750), Amiloride (Sigma-Aldrich, Cat# A7410), Click-iT TUNEL Alexa Fluor 488 imaging assay kit (ThermoFisher Scientific Cat# C10245), DRAQ5 (Abcam, Cat# ab108410), Fluoromount (Sigma-Aldrich, Cat# F4680), DNA/RNA/miRNA Universal Kit (Qiagen, Cat# 80224),
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4

Cytotoxicity Screening of Model Compounds

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Hep3B human hepatoma cell line was obtained from ATCC (Manassas, VA). RPMI-1640 and model compounds, including acetaminophen, lovastatin, rotenone, tamoxifen, menadione, and sodium citrate, were purchased from Sigma Aldrich (St. Louis, MO). Coating materials including poly(maleic anhydride alt-1-octadecene) (PMA-OD), 0.01% poly-L-lysine (PLL), and barium chloride (BaCl2) were also purchased from Sigma Aldrich. Fluorescent probes, including calcein AM, tetramethyl rhodamine methyl ester (TMRM), Hoechst 33342, and monochlorobimane (mBCl), were purchased from Thermo Fisher Scientific (Waltham, MA). Fetal bovine serum (FBS) was purchased from Corning (Tewksbury, MA).
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5

Isolated Rat Aorta Protocol

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For chemicals, acetylcholine chloride (ACh), cesium chloride (CsCl), p-cymene (Figure 1), glibenclamide, dimethyl sulphoxide (DMSO), phenylephrine hydrochloride (PE), tetraethylammonium chloride (TEA), 4-aminopyridine (4-AP), and barium chloride (BaCl2) were purchased from Sigma-Aldrich (St. Louis, MO, USA). All salts used in Krebs solution were purchased from Vetec QuímicaFina Ltda. (Duque de Caxias, RJ, Brazil). p-Cymene was dissolved in DMSO (100%) and diluted in distilled water according to the requirements of each experiment.
For all experiments with isolated rat aorta, Krebs salt solution was used, with the composition and concentration (in mM) as follows: NaCl (118), KCl (4.6), MgSO4·7H2O (5.7), NaH2PO4·H2O (1.1), CaCl2 (2.5), NaHCO3 (25), and glucose (11) with pH adjusted to 7.4 with 1 N HCl solution.
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6

Alginate-Based Hydrogel Synthesis Protocol

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Tests were carried out using salt of alginate acid (Sigma-Aldrich, Poznan, Poland) with the following parameters: viscosity 15–25 cP, 1% H2O, pH 6.5–8.5, molecular weight 120–190 g/mol and density 1.601 g/cm3 and calcium chloride CaCl2 and barium chloride BaCl2 (Sigma-Aldrich, Poznan, Poland). Chemical reagents needed for the preparation of artificial urine solution according to Mayrovitz and Sims [53 (link)]: urea (Sigma-Aldrich, Poznan, Poland), creatinine (Sigma-Aldrich, Poznan, Poland), sodium chloride NaCl (Sigma-Aldrich, Poznan, Poland), ammonium chloride NH4Cl (Chempur, Poland), sodium sulfate Na2SO4 (Avantor Performance Materials Poland S.A., Gliwice, Poland) and di-sodium phosphate (Avantor Performance Materials Poland S.A., Gliwice, Poland). All the solutions were prepared in deionized water.
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7

Characterizing Bioactive Lipid Compounds

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Arachidonic acid (AA), BL-1249, CDC, cis-4,7,10,13,16,19-docosahexaenoic acid (DHA), and barium chloride (BaCl2) were purchased from Sigma-Aldrich, spadin was bought from Tocris. All substances, except BaCl2, were stored as stocks (1 mM–1 M) at −20°C and diluted to the required concentrations in standard bath solution immediately prior to experimentation.
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8

Microtubule Disruption and Cell Stress

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Nocodazole (Sigma); Dexamethasone (Dex; Sigma); Rose Bengal Lactone (RBL; Sigma); and Barium Chloride (BaCl2; Sigma).
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9

Molecular Cloning Using E. coli

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Amberlyst-15 and barium chloride (BaCl2) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Sulfuric acid (H2SO4) was acquired from Samchun Chemicals (Seoul, Korea). E. coli XL1-Blue competent cells were purchased from Stratagene (La Jolla, CA). The genes used for plasmid construction were obtained through gene synthesis by Cure Bio (Seoul, Korea).
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10

Vascular Function Drug Interactions

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The following drugs were used in this experiment: Nω-nitro L-arginine methyl ester (L-NAME), indomethacin, acetylcholine hydrochloride (ACh), phenylephrine, catalase, baicalein, 18 alpha-glycyrrhetinic acid (18α-GA), ouabain, glibenclamide, barium chloride (BaCl2), (all purchased from Sigma-Aldrich Chemie GmbH, Steinheim, Germany), 17-octadecynoic acid (17-ODYA) and 1-[(2-chlorophenyl) diphenylmethyl]-1H-pyrazole (TRAM-34) (Tocris Bioscience, Bristol, UK), iberiotoxin (IbTX), charybdotoxin (ChTX) and apamin (AnaSpec Inc., Fremont, CA, USA), margatoxin (MgTX), α- and β-dendrotoxin (α- and β- DTX) (Alomone Labs, Jerusalem, Israel). indomethacin, 17-ODYA, baicalein, glibenclamide and TRAM-34 were dissolved in dimethyl sulfoxide (DMSO). 18α-GA was dissolved in chloroform: ethanol (2:3) according to the manufacturer’s instructions. Apamin, ChTX, IbTX and L-NAME were dissolved in phosphate-buffered saline (PBS), whereas all other drugs were dissolved in distilled water.
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