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25 protocols using boric acid

1

Oligonucleotide Synthesis and Purification Protocols

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All synthetic oligonucleotides were purchased from Eurofins. PCR primers were desalted, DNAzymes were purified by Eurofins proprietary High Purity Salt Free reverse phase cartridge purification system and short RNA substrates were purified by HPLC. RNase-free ultrapure water was produced using a Milli-Q Advantage A10 Water Purification System equipped with a BioPak® Polisher from Merck Millipore. Phusion High-Fidelity PCR kit and TranscriptAid T7 High Yield Transcription kit were from Life Technologies. 4-(2-Hydroxyethyl)piperazine-1-ethanesulfonic acid (HEPES), sodium chloride, manganese chloride tetrahydrate, formamide, bromophenol blue, 40% 19:1 acrylamide/bis-acrylamide, N,N,N′,N′-tetramethylethylenediamine, ammonium persulfate, urea, agarose, ethidium bromide and phenol:chloroform:isoamyl alcohol 25:24:1 pH 8.0 was purchased from Sigma-Aldrich. Ethylenediaminetetraacetic acid (EDTA) and sodium dodecyl sulfate (SDS) were from Scharlau. Boric acid was from VWR. Klorrent bleach was from Nilfisk. The nucleic acid dyes SYTO 61, PO-PRO 1, DRAQ5, Hoechst 33258, DAPI, Propidium iodide and PicoGreen were all from Life Technologies. GelRed was from Biotium. ethidium bromide was from Sigma.
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2

Lignite Characterization from Choa Saiden Shah

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The lignite was collected
from Choa Saiden Shah Coal Mines, Chakwal (Pakistan).
All the chemicals used in this experiment were of reagent grade. The
urea, boric acid, starch, and PVA were purchased from VWR International
(USA), and C-SRF was purchased from Fatima Fertilizer Limited, Pakistan.
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3

Distillation Unit System Characterization

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We purchased the distillation unit system from VWR International Ltd., Radnor, PA, USA.
The sulfuric acid (c(H2SO4) = 18 mol/L, ρ20(H2SO4) = 1.84 g/mL), the boric acid (aqueous solution, [ρ20(H3BO3) = 40 g/L]), and the catalyst (CuSO4·5H2O) were all bought in Hungary from different lab supply retailers. The items varied depending on where they originated (Vwr International Kft, Debrecen, Hungary and Thermo Fisher Scientific, Budapest, Hungary).
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4

Electrochemical Analysis of Cocaine in Street Samples

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The cocaine·HCl standard was purchased from Lipomed (Arlesheim, Switzerland). Standards of phenacetin, diltiazem, lidocaine, procaine, hydroxyzine, benzocaine, paracetamol and myo-inositol were purchased from Sigma-Aldrich (Diegem, Belgium). Standards of benzoic acid and levamisole were purchased from Acros Organics (Geel, Belgium). Standards of caffeine, boric acid, glucose, maltose and starch were purchased from VWR Chemicals (Leuven, Belgium) and a standard of d-sorbitol was purchased from Merck Chemicals KGaA (Overijse, Belgium). Authentic cocaine street samples were obtained from the National Institute for Criminalistics and Criminology (Brussels, Belgium). Gelatine gel B was supplied by PB gelatins (United Kingdom). Carbon ItalSens IS-C Screen Printed Electrodes (SPE) were purchased from PalmSens (Utrecht, The Netherlands) and were used during all electrochemical measurements. The electrode surface area is 7.07 mm2. All laboratorium-based electrochemical measurements were performed using a Metrohm μAutolab III Potentiostat and NOVA 1.11 software.
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5

Quantification of Heavy Metals in Secondary Lead

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The slag and matte were kindly provided by a European secondary lead producer. Disodium ethylenediaminetetraacetic acid (0.1 mol L−1, Na2EDTA) and sodium hydroxide (NaOH, pearl) was purchased from Fisher Scientific (Loughborough, United Kingdom). Disodium ethylenediaminetetraacetic acid (0.2 mol L−1, Na2EDTA) was purchased from Honeywell Fluka (Seelze, Germany). Hydrochloric acid (37 wt%, HCl in water) and boric acid (99.5%, H3BO4 in water) was supplied by VWR Chemicals (Leuven, Belgium). Nitric acid (65 wt% HNO3 in water) and iron, lead, zinc and rhodium standard solutions (1000 mg L−1) were purchased from Chem-Lab NV (Zedelgem, Belgium). Hydrofluoric acid (48 wt%, HF in water) and ammonium sulfide (20 wt%, (NH4)2S in water) were purchased from Sigma-Aldrich (Diegem, Belgium). All chemicals were used as received without any further purification.
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6

Synthesis of Nickel-Chelating Resins

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Anhydrous solvents CH2Cl2, EtOH and MeOH were purchased from Acros Organics. Anhydrous sodium sulfate, sodium borohydride, boric acid and sulfuric acid were from VWR, nickel (II) chloride (NiCl2.6H2O) was from Acros Organics, 25% sodium methoxide solution in MeOH , ethylene diamine, glutaraldehyde (25% in H2O), amberlite IR120(H + ) and anthrone were purchased from Sigma-Aldrich.
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7

Quantitative Analysis of Antioxidants

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The chemicals [2,2-diphenyl-1-picrylhydrazyl; 2′-azino-bis (3-ethylbenzothiazoline- 6-sulfonic acid); 2,4,6-Tris(2-pyridyl)-s-triazine], reagents (Folin–Ciocalteu reagent), standards: ferulic acid, ellagic acid, proline, tyrosine, glycine, lysine, histidine, leucine, aspartic acid, valine were obtained from Sigma Aldrich (St., MO, USA), Elisa kits for testosterone and estradiol from Abbexa (Cambridge, UK) and buffer components (chloroform, ethyl acetate, formic acid, ethanol, 1-butanol, 2-propanol, boric acid) were purchased from Avantor Performance Materials Poland SA (APM, Gliwice, Poland).
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8

Lipid Membrane Characterization Across pH Range

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Phosphatidylcholine (DPPC) and phosphatidylethanolamine (DPPE) of 99% purity were acquired from Sigma-Aldrich (Darmstadt, Germany). With the use of a 20 mg/mL lipid in a n-decane/butanol mixture (3:1) solution, the membrane was created using the Mueller and Rudin method [33 (link)].
As the electrolyte solution, the buffer was used in the pH range of 2–12 prepared according to Britton and Robinson [34 (link)]. The buffer was prepared by adding 0.2 M sodium hydroxide to 100 mL of the solution (initial pH was 1.81) with the following composition: 0.04 M 80% acetic acid, 0.04 M phosphoric acid, and 0.04 M boric acid (all chemicals from Avantor Performance Materials Poland, Gliwice, Poland).
The proper pH of the buffer was determined depending on the amount of sodium hydroxide added. Buffer pH was changed to, e.g., 3.29 after the addition of 20 cm3 NaOH (Avantor Performance Materials Poland, Gliwice, Poland) or to 6.80 if 50 cm3 was added. The buffer, as mentioned previously, was used in the experiments because it is widely used in biological studies as a standard buffer due to the wide pH range (2–12) and a composition that does not affect the biological membrane.
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9

Lanthanum Removal by Chitosan Adsorption

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A basic standard solution of boron in the form of boric acid (1 g/dm3) and a basic standard solution of lanthanum in the form of lanthanum nitrate (1 g/dm3) were supplied by Merck KGaA, Darmstadt, Germany. Chitosan (molecular weight of 600,000–800,000 g/mol) was purchased from Acros Organics, Geel, Belgium; the degree of deacetylation of CTS, as determined by means of a H1 NMR method, was equal to 97%. lanthanum nitrate, La(NO3)3·6H2O, was supplied by Reachim Ltd., Moscow, Russian Federation. boric acid, sodium hydroxide, hydrochloric acid, and glacial acetic acid were purchased from Avantor Performance Materials Poland S.A., Gliwice, Poland. All the reagents employed in the study were analytical reagent grade.
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10

Chitosan-Based Analytical Reagent Preparation

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Chitosan (molecular weight 600,000–800,000) was purchased from Acros Organics (Geel, Belgium); its degree of deacetylation, determined by a 1H NMR method, was 97%. Manganese chloride, MnCl2·4H2O, and other reagents, namely potassium nitrate, sodium hydroxide, and hydrochloric acid, were supplied by Avantor Performance Materials Poland S.A., Gliwice, Poland. A working boron solution of a concentration of 5 g/L was prepared using boric acid provided by Avantor Performance Materials Poland S.A., Gliwice, Poland. A basic standard solution of boron in the form of boric acid (1 g/L) and a manganese standard solution of 1 g/L were supplied by Merck.
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