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Ethylenediaminetetraacetic acid

Manufactured by Thermo Fisher Scientific
Sourced in United States, United Kingdom, Germany

Ethylenediaminetetraacetic acid (EDTA) is a chemical compound used as a chelating agent. Its core function is to form stable complexes with metal ions, effectively binding and sequestering them.

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103 protocols using ethylenediaminetetraacetic acid

1

Cardiac Function Assessment in Mice

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At the end of in vivo treatments (4 or 6 weeks), mice underwent carbon dioxide asphyxiation. After mice ceased breathing, they were weighed and transferred to an operation bench. The death was confirmed by cervical dislocation. Subsequently, blood was collected through the abdominal aorta and hearts were collected through a thoracic incision. Blood samples were immediately supplemented with 0.1% ethylenediaminetetraacetic acid (Fisher Scientific) and stored at −20°C for future serotonin enzyme-linked immunosorbent assay. Hearts were washed at least 3 times in phosphate-buffered saline [PBS, 137 mM sodium chloride, 2.7 mM potassium chloride, 4.3 mM sodium phosphate dibasic and 1.46 mM potassium phosphate monobasic (all from Fisher Scientific)] supplemented with 0.1% ethylenediaminetetraacetic acid, followed by fixation in 4% formaldehyde (Fisher Scientific). Paired Student’s t-test was performed to assess the significant differences on animal weight changes with age. P < 0.05 were considered significant.
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2

Antibacterial Susceptibility Testing Protocol

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Ethylenediaminetetraacetic acid (EDTA) and sodium chloride were purchased from Fisher Scientific (Pittsburgh, PA). TIG was obtained from TSZ CHEM (Framingham, MA). TET, and trimethoprim (TMP) were obtained from Medisca Incorporated (Plattsburgh, New York). Oxytetracycline (OXY), chlortetracycline (CHL), and magnesium chloride were obtained from Sigma-Aldrich Corporation (St. Louis, MO). Calcium chloride was obtained from Allied Chemical Corporation (Morristown, NJ) and Fisher Scientific (Pittsburgh, PA). Bacterial dispersions in normal saline were prepared using the A-JUST Turbidimeter (Abbott Laboratories) along with McFarland Turbidity Standards (Remel Microbiology Products, Lenexa, KS). Cation-adjusted Mueller Hinton Broth was obtained from Becton, Dickinson and Company (Sparks, MD). Pseudomonas aeruginosa ATCC® 27853 and a tetracycline-resistant methicillin-resistant Staphylococcus aureus isolate were provided by UF Health Microbiology Laboratory (Gainesville, FL), and clinical isolates Escherichia coli ARC3600 (NDM-1, CMY-6, OXA-1) and Klebsiella pneumoniae ARC3802 (NDM-1, SHV-2a, SHV-11, CTX-M-15, TEM-1) were provide by JMI Laboratories (North Liberty, IA).
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3

Characterization of Advanced Glycation Endproducts

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Ethylenediaminetetraacetic acid was obtained from Fisher Scientific International, UK. Aged garlic extract was kindly provided by Wakunaga of America Company Ltd. Ribose, sodium dodecyl sulphate (SDS) and Tris (hydroxymethyl)-amino methane were obtained from BDH, UK. Acrylamide solution was obtained from Bio-Rad Laboratories (Hemel Hempstead, UK). Bromophenol blue was obtained from Serva, Germany. Ethanol, glacial acetic acid and mEthanol were obtained from Fisher Scientific International, UK. Dialysis tubing with a molecular weight cut off of 3.5 kDa and 67 kDa was obtained from Medical International Ltd Company (London, UK). Advanced glycation endproduct antibody (rabbit polyclonal to AGE antibody) and rabbit IgG secondary antibody (goat polyclonal to rabbit IgG) were purchased from Abcam, UK. All other reagents were of analytical reagent grade from Sigma-Aldrich Company (Poole, UK).
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4

Quantitative Analysis of MDPV Analogs

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MDPV and MDPV-d8 were obtained from Cayman Chemical Company (Ann Arbor, MI, USA) and Cerilliant (Round Rock, TX, USA). 3,4-Catechol-PV and 4-OH-3-MeO-PV were synthesized and purified by the Drug Design and Synthesis Section of the National Institute on Drug Abuse (NIDA) Intramural Research Program (IRP), Baltimore, MD, USA (Anizan et al. 2014 (link)). Formic acid, methanol, LC-MS grade acetonitrile (ACN) and water, ethylenediaminetetraacetic acid (EDTA) and sodium metabisulfite (SMBS) were acquired from Fisher Scientific (Fair Lawn, NJ, USA). 4-Methylcatechol and sodium hydroxide were purchased from Sigma (St Louis, MO, USA) and JT Baker (Phillipsburg, NJ, USA), respectively. β-glucuronidase from Red Abalone was obtained from Kura Biotec (Culver City, CA, USA). Water for EDTA, 4-Methylcatechol and SMBS solution preparation was purified-in-house by an ELGA Purelab Ultra Analytic purifier (Siemens Water Technologies, Lowell, MA, USA).
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5

Comprehensive Characterization of MDPV and Metabolites

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MDPV and MDPV-d8 were obtained from Cayman Chemical Company and Cerilliant. 3,4-catechol-PV and 4-OH-3-MeO-PV were synthesized and purified by the Drug Design and Synthesis Section of the National Institute on Drug Abuse (NIDA) Intramural Research Program, Baltimore, MD, USA. Formic acid, methanol, acetonitrile, water, ethylenediaminetetraacetic acid (EDTA) and sodium metabisulfite (SMBS) were acquired from Fisher Scientific. 4-methylcatechol and sodium hydroxide were purchased from Sigma and JT Baker, respectively. β-glucuronidase from Red Abalone was obtained from Kura Biotec. Water for EDTA, 4-methylcatechol and SMBS solution preparation was purified-in-house by an ELGA Purelab Ultra Analytic purifier.
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6

Hybrid Membrane Fabrication and Characterization

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Polyvinyl alcohol (Sigma Aldrich Chemical Company, St. Louis, MO, USA) was purchased as a fully hydrolyzed powder with an average molecular weight of 85,000 g/mol. For the hybrid method, CA membranes were commercially purchased from Fisher Scientific Company (Waltham, MA, USA) with a symmetrical pore size of 0.45 µm and a diameter of 47mm. The tridentate chelator, iminodiacetic acid (IDA), and 50% (w/w) GA were also purchased from Sigma-Aldrich Chemical Company. Bovine serum albumin, sulfuric acid, copper sulfate, silver nitrate, ethylenediaminetetraacetic acid (EDTA), acetic acid, and sodium bicarbonate were purchased from Fisher Scientific Company. All materials were used without further purification.
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7

Thermal Equilibrium Measurements and Hyperpolarized Dissolutions

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14.1T thermal equilibrium measurements and hyperpolarized dissolutions were performed with a D2O- or H2O-based buffer. Each buffer consisted of 100mM Tris base and 1mM ethylenediaminetetraacetic acid (Fisher Scientific, USA). H2O-based buffers were adjusted to pH 7.4 with conc. HCl and 10N NaOH (Fisher Scientific, USA) and D2O-based buffers were adjusted to pD 7.4 with conc. DCl and 10N NaOD (Sigma-Aldrich, USA). pH and pD of H2O- and D2O-based buffers were measured with a Ag/AgCl electrode (Fisher Scientific, USA). Since the ionization constants of H2O and D2O (13.99 and 14.96)23 and reduction potentials of H+ and D+ (0V and −0.044V)24 are similar, we assumed that an Ag/AgCl pH electrode could be used to roughly approximate pD.
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8

Peptide Synthesis and Biological Assays

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All required organic solvents and fatty acids were purchased from Wilkem Scientific (Pawtucket, RI, USA). Coupling reagents, Rink amide MBHA resin, and Fmoc-amino acid building blocks were purchased from Chem-Impex International Inc. (Wood Dale, IL, USA). 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (catalog # M2128) was from Sigma (St. Louis, MO). Hanks balanced salt solution (HBSS), Dulbecco’s modified Eagle medium (DMEM; low glucose with L-glutamine), RPMI -1640 medium with L-glutamine, fetal bovine serum (FBS), SYBR Green II solution, penicillin (10000 U/mL), Lipofectamine® 2000, and streptomycin (10 mg/mL) were provided by Life Technologies (Grand Island, NY). Scrambled negative control siRNA (catalog # AM4635), 5′-carboxyfluorescein (FAM)-labeled negative control siRNA (catalog # AM4620), and the siRNA targeting kinesin spindle protein (KSP; catalog # AM16704) were obtained from Ambion (Austin, TX). All the primers were purchased from IDT. Heparin sodium salt from porcine intestinal mucosa was purchased from Alfa Aesar (Ward Hill, MA). PCR master mixes iScriptTM reverse transcription supermix and iTaq universal SYBR® Green supermix were purchased from Bio-Rad (Hercules, CA). Ethylenediaminetetraacetic acid (EDTA) and all other requirements were provided by Fisher Scientific (Carlsbad, CA).
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9

PEI-Mediated Cytotoxicity and Transfection

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Hyperbranched polyethylenimine (PEI, 25 kDa) was obtained from BASF (Ludwigshafen, Germany). RPMI-1640 medium with L-glutamine and sodium bicarbonate, Dulbecco’s phosphate buffered saline (PBS), heat-inactivated fetal bovine serum (FBS), D-(+)-glucose, sodium bicarbonate, picrylsulfonic acid (TNBS) solution 5%, sodium pyruvate, 2-mercaptoethanol, dimethyl sulfoxide (DMSO, ≥99.7%), ethylenediaminetetraacetic acid (EDTA, 99.4-–100.06%), trypan blue (0.4%, sterile filtered) and bulk DNA (bDNA) from salmon sperm (6000 kDa, Fisher Scientific) were purchased from Sigma-Aldrich (Munich, Germany). SYBR Gold dye was obtained from Life Technologies (Carlsbad, CA, U.S.A.).
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10

Synthesis and Characterization of Tungsten Oxide Nanoparticles

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Tungsten oxide (WO3, orthorhombic crystal) nanoparticles (spherical, 23–65 nm in diameter, and 99.95% purity) were purchased from US Research Nanomaterials (USA). Pyridine and toluene were purchased from Alfa Aesar (USA). (3-aminopropyl)triethoxysilane (APTES, 99%) was purchased from Sigma-Aldrich (USA). Cadmium chloride anhydrous, lead chloride, ethylenediaminetetraacetic acid (EDTA), and tris (hydroxymethyl)aminomethane were purchased from Fisher Scientific (USA). Diethyl ether and sodium dihydrogen phosphate were purchased from Acros Organics (Geel, Belgium). Standard Suwannee River natural organic matter (NOM) was obtained from the International Humic Substances Society (IHSS, USA). A NOM stock solution (100 mg/L) was prepared by mixing a known amount of NOM with DI water for 24 h. The pH of the stock solutions was adjusted to 8 with 0.1 M and 0.01 M NaOH and HCl. All chemicals were used as received, without further purification. All solutions were prepared with deionized water (18 MΩ-cm) from a Barnstead NANOpure Diamond water purification system (USA).
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