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3 4 dihydroxyphenethylamine hydrochloride

Manufactured by Merck Group

3,4-dihydroxyphenethylamine hydrochloride is a chemical compound used in various scientific research applications. It is a white crystalline solid with the molecular formula C8H11NO2·HCl. The compound is used as a laboratory standard and reagent in analytical and biochemical studies.

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3 protocols using 3 4 dihydroxyphenethylamine hydrochloride

1

Lipid Composition for Membrane Studies

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1,2-Dioleoyl-sn-glycero-3-phosphocholine
(DOPC), 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine
(DOPE), egg sphingomyelin (Sm), and cholesterol (Chol) were obtained
from Avanti Polar Lipids (Alabaster, AL), and 1,2-dioleoyl-sn-glycero-3-phospho-l-serine (DOPS) was obtained
from Larodan AB (Solna, Sweden). 3,4-Dihydroxyphenethylamine hydrochloride
(dopamine), 3,4-dihydroxy-l-phenylalanine (l-dopa,
levodopa), 3-methoxy-4-hydroxyphenethylamine hydrochloride (3-methoxytyramine,
3-MT), 3,4-dihydroxy-4′-methyl-5-nitrobenzophenone (tolcapone),
2-cyano-N,N-diethyl-3-(3,4-dihydroxy-5-nitrophenyl)propenamide
(entacapone), l-ascorbic acid, sodium chloride (NaCl), calcium
chloride (CaCl2), 4-(2-hydroxyethyl)-1-piperazineethanesulfonic
acid (HEPES), chloroform (CHCl3), 3-[(3-cholamidopropyl)
dimethylammonio]-1-propanesulfonate (CHAPS), and ethylenediaminetetraacetic
acid (EDTA) were from Sigma-Aldrich (St. Louis, MO). Ion-exchanged
ultrapure water (H2O) with a resistivity of 18 MΩ cm
from a Milli-Q purification system was used for the preparation of
all solutions.
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2

Immobilization and Release of BMP-2 on Microcarriers

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Bone morphogenetic protein 2 (BMP-2) was immobilized onto microcarriers through their surface treatment using poly(3,4-dihydroxyphenethylamine) (PDA). Microcarriers were immersed in 2 mg/mL 3,4-dihydroxyphenethylamine hydrochloride (Sigma-Aldrich) dissolved in a 10 mM Tris buffer for 6 h with mild shaking. The microcarriers were then separated and washed with deionized water. Subsequently, functionalized microcarriers were incubated in 500 ng/mL BMP-2 solution at 37 °C under mild shaking overnight. Microcarriers were then washed with sterile PBS, freeze-dried and stored in a sterile condition for further usage. The immobilization efficiency of BMP-2 was measured based on washout BMP-2 content by an ELISA kit (Cell Applications Inc.) as described elsewhere19 (link). The content of BMP-2 was recorded as ng/ml of solution. In order to study BMP-2 release profile, the conjugated microcarriers were suspended in 1 mL PBS at pH 7.4, and incubated at 37 °C. At scheduled time during 28-days following incubation time, a release sample was collected and replaced with the same volume of fresh filtered medium.
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3

HPLC Analysis of Neurotransmitters

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Monobasic sodium phosphate, disodium ethylenediamine tetraacetate (Na2EDTA), 85% o-phosphoric acid, acetonitrile, methanol, hydrochloric acid (HCl), sodium hydroxide (NaOH), and 0.3 μm alumina powder were obtained from Fisher Scientific (Pittsburgh, PA). Ammonium acetate, 1-octanesulfonic acid [sodium salt] (SOS), sodium tetraborate decahydrate, boric acid, lithium tetraborate, lithium dodecyl sulfate (LDS), tetradecyltrimethylammonium bromide (TTAB), β-alanine (β-Ala), sodium cyanide, 4-hydroxybenzoic acid (4-HBA), L-glutamic acid (Glu), L-aspartic acid (Asp), L-arginine (Arg), γ-amino-n-butyric acid (GABA), DL-2-aminoadipic acid (AAP), sodium cyanide, 3,4-dihydroxybenzylamine (DHBA), 3,4-dihydroxyphenethylamine hydrochloride (DA), L-arterenol (NE), homovanillic acid (HVA), 3,4-dihydroxyphenylacetic acid (DOPAC), 5-hydroxytryptamine (5-HT), 5-hydroxyindoleacetic acid (5-HIAA) were obtained from Sigma-Aldrich (St. Louis, MO). Naphthalene-2,3-dicarboxaldehyde (NDA) was obtained from Invitrogen (Carlsbad, CA). All solutions were prepared in 18.2 MΩ distilled, deionized water (Labconco, Kansas City, MO) and filtered through 0.22 μm pore size membrane filters prior to use unless otherwise noted.
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