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Cadaverine dihydrochloride

Manufactured by Merck Group
Sourced in United States

Cadaverine dihydrochloride is a chemical compound used in various laboratory applications. It serves as a precursor for the synthesis of other chemical compounds and is utilized as a research tool in specialized fields. The core function of this product is to provide a reliable and well-defined source of the cadaverine molecule for laboratory experiments and analysis.

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27 protocols using cadaverine dihydrochloride

1

Quantification of Biogenic Amines

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Biogenic amines standards methylamine hydrochloride 99% (MA), ethylamine hydrochloride 98%(EA), dimethylamine hydrochloride 99% (DMA), diethylamine hydrochloride 99% (DEA), propylamine hydrochloride 99% (PA), butylamine 99% (BA), 2-phenylethylamine hydrochloride 98% (PHA), tyramine hydrochloride 98% (TYR), tryptamine hydrochloride 99% (TRP), histamine dihydrochloride 99% (HIS), hexylamine 99%(HEA), isopentylamine 99% (isoPA), putrescine dihydrochloride 98% (PUT), cadaverine dihydrochloride 98% (CAD),spermidine trihydrochloride 99.5%(SPD), spermine tetrahydrochloride 99.5% (SPE), agmatine sulfate 98% (AGM) were obtained from Sigma Aldrich (St. Louis, MO, USA). The internal standard (IS) was 1.7-diamoheptane 98% (DAH) purchased from Sigma Aldrich (St. Louis, MO, USA). Formic acid (FA) was obtained from Merck (Darmstadt, Germany). Boric acid and sodium hydroxide were purchased from POCH (Gliwice, Poland). Acetonitrile (ACN) with LC-MS grade, ammonium formate and tosyl chloride (≥99%) were obtained from Sigma Aldrich (St. Louis, MO, USA). Nylon Captiva Econofilters (25 mm diameter, 0.2 µm pore size) were purchased from Agilent Technologies (Santa Clara, CA, USA). Ultrapure water was produced by the HLP5 system from Hydrolab (Wiślina, Poland).
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2

Proteomic Analysis of Modified Proteins

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All reagents and solvents were purchased at the highest purity available. Cadaverine dihydrochloride, 2HP dihydrochloride, horseradish peroxidase (HRP), ethanol, 4-vinylpyridine, ammonium citrate, and citric acid were purchased from Sigma-Aldrich (St. Louis, MO, USA). Boric acid, sodium borate, and N-acetyl-3,7-dihydroxyphenoxazine (Amplex™ Red Reagent) were obtained from Thermo Fisher Scientific (Lenexa, KS, USA). Optima™ LC/MS-grade acetonitrile, water, and formic acid were purchased from Fisher Scientific (Thermo Fisher Scientific). Sequencing grade trypsin, chymotrypsin, and glycerol-free peptidyl-N-glycosidase F (PNGase F) were purchased from Promega (Madison, WI, USA) and New England BioLabs (Ipswich, MA, USA), respectively. Deionized water with a resistivity of 18 MΩ∙cm was purified using a Millipore Direct-Q3 Water Purification System (Billerica, MA, USA).
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3

Biogenic Amine Quantification Protocol

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Tryptamine, β-phenylethylamine hydrochloride, putrescine dihydrochloride, cadaverine dihydrochloride, histamine dihydrochloride, tyramine hydrochloride, spermidine trihydrochloride, and spermine tetrahydrochloride (all Sigma-Aldrich) were used for standard solutions, and 1,7-diaminoheptane (Sigma-Aldrich) was applied for an internal standard. The concentrations of all standard solutions were adjusted to 0, 10, 50, 100, and 1000 ppm.
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4

Quantification of Biogenic Amines

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All chemicals, unless otherwise stated, were of the highest quality and were used as supplied. All the standard biogenic amines (putrescine dihydrochloride, agmatine sulfate, histamine dihydrochloride, 2-phenylethylamine, tyramine hydrochloride, spermine tetrahydrochloride, tryptamine hydrochloride, spermidine trihydrochloride and cadaverine dihydrochloride) were purchased from Sigma-Aldrich (St. Louis, MO, USA). High-performance liquid chromatography (HPLC) grade ammonium acetate and acetonitrile were purchased from Merck (Damstadt, Germany).
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5

Biogenic Amine Analysis by HPLC

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All chemicals and solvents were of the analytical and chromatographic grade. Standard biogenic amines (agmatine sulfate, tryptamine hydrochloride, 2-phenylethylamine, putrescine dihydrochloride, cadaverine dihydrochloride, histamine dihydrochloride, tyramine hydrochloride, spermidine trihydrochloride, and spermine tetrahydrochloride), dansyl chloride, and acetone were purchased from Sigma-Aldrich (St. Louis, MO, USA). Sodium hydroxide, sodium hydrogen carbonate, ammonium hydroxide, and perchloric acid were purchased from Junsei Chemicals (Tokyo, Japan). High-performance liquid chromatography (HPLC) grade acetonitrile and ammonium acetate were obtained from Merck (Darmstadt, Germany). Nutrient agar was purchased from Difco (Sparks, MD, USA). API kits were purchased from BioMerieux (Marcy I’ Etoile, France).
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6

Biogenic Amine Detection and Analysis Protocol

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Biogenic amine standards (histamine dihydrochloride (HIS), tryptamine hydrochloride (TRP), 2-phenylethylamine (2-PHE), putrescine dihydrochloride (PUT), cadaverine dihydrochloride (CAD), tyramine hydrochloride (TYR), spermidine trihydrochloride (SPD), and spermine tetrahydrochloride (SPM)) and dansyl chloride were obtained from Sigma-Aldrich Chemical Co. (St. Louis, MO, USA). Perchloric acid, 25% ammonium hydroxide solution, sodium hydroxide sodium hydrogen carbonate, and diethyl ether were acquired from Daejung Chemical Co. (Siheung, Korea). Acetone and acetonitrile (High-performance liquid chromatography (HPLC) grade) were purchased from Tedia Co. (Fairfield, OH, USA). Compound mixtures of amino acids, borate buffer, o-phthalaldehyde (OPA) and 9-fluorenylmethoxycarbonyl chloride (FMOC-Cl) were obtained from Agilent Technologies (Andover, MA, USA).
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7

Spectrophotometric Determination of DAO Activity

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Diamine oxidase (DAO) activity in plasma was determined using spectrophotometry as described by Hosoda et al. (1989) (link). The assay mixture (3.8 mL) contained 3 mL of phosphate buffer (0.2 M, pH 7.2), 0.1 mL (0.004%) of horseradish peroxidase solution (Sigma Chemicals), 0.1 mL of o-dianisidine–methanol solution (0.5% of o-dianisidine [Sigma Chemicals] in methanol), 0.5 mL of plasma, and 0.1 mL of substrate solution (0.175% of cadaverine dihydrochloride, Sigma Chemicals). This mixture was incubated for 30 min at 37°C, and absorbance at 436 nm was measured to indicate DAO activity.
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8

Synthesis and Characterization of Gold Nanoparticles

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Chloroauric acid tetrahydrate (HAuCl4·4H2O) was purchased from Sangon Biotech (Shanghai, China). Histamine dihydrochloride, histidine, putrescine dihydrochloride, cadaverine dihydrochloride, 2-Phenylethylamine hydrochloride, and tyramine hydrochloride were obtained from Sigma (St. Louis, MO, USA) (http://www.sigmaaldrich.com). Trisodium citrate and NaCl were purchased from Tianjin Chemical Reagent Co., Ltd. (Tianjin, China). Salmon samples were purchased from a local aquatic products market. Moreover, Milli-Q-purified water (18.2 MΩcm) was used throughout the experiments.
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9

Quantification of Bilirubin Metabolism Enzymes

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Rabbit anti-occludin polyclonal IgG was acquired from Santa Cruz Biotechnology (CA, USA). Rabbit anti-glyceraldehyde 3-phosphate dehydrogenase (GAPDH) polyclonal IgG was purchased from XianZhi Biotechnology (Hangzhou, China). Rabbit anti-β-actin polyclonal IgG was acquired from Biosynthesis Biotechnology (Beijing, China), Horseradish peroxidase-labeled goat anti-rabbit IgG was obtained from ZSGB-Bio (Beijing, China).
Unconjugated bilirubin (UCB), biliverdin hydrochloride, peroxidase (POD), o-dianisidine dihydrochloride, cadaverine dihydrochloride, nicotinamide adenine dinucleotide (NAD), diamine oxidase (DAO) standard and D-Lactic dehydrogenase (D-Lac) standard were obtained from Sigma-Aldrich (Shanghai, China). Bilirubin ditaurate disodium was purchased from Frontier Scientific (Logan, Utah, USA). Dulbecco's phosphate buffered saline (PBS) and pentobarbital sodium were purchased from Solarbio (Beijing, China). All other reagents and solvents were purchased from J&k scientific (Beijing, China).
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10

Quantitative Analysis of Biogenic Amines

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Stock standard solutions of BA, including tryptamine, β-phenylethylamine hydrochloride, putrescine dihydrochloride, cadaverine dihydrochloride, histamine dihydrochloride, tyramine hydrochloride, spermidine trihydrochloride, and spermine tetrahydrochloride (all from Sigma-Aldrich), were separately prepared at 10,000 mg/L concentration in deionized water. Working solutions at 1000 mg/L concentration were prepared by diluting 1 mL of each stock solution in deionized water to bring to a final volume of 10 mL. The concentrations of all standard solutions used were 0, 10, 50, 100, and 1000 mg/L. In addition, 1,7-diaminoheptane (Sigma-Aldrich) served as an internal standard.
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