Search results for "High Pressure"

showing 10 items of 894 documents

Characterization of a cDNA encoding RP43, a CUB-domain-containing protein from the tube of Riftia pachyptila (Vestimentifera), and distribution of it…

2000

A major 43kDa protein from the protective tube of Riftiapachyptila (Vestimentifera), named RP43, was partly microsequenced after isolation by SDS/PAGE from the protein fraction of tubes collected around the hydrothermal vents at the East Pacific Rise. On the basis of the partial peptide sequences obtained, experiments using reverse-transcriptase-mediated PCR and rapid amplification of cDNA ends led to the complete cDNA sequence. Analysis of deduced amino acid sequence of RP43 showed the presence of CUB domains (100–110-residue-spanning domains first reported in the complement subcomponents C1r/C1s, epidermal-growth-factor-related sea urchin protein and bone morphogenetic protein 1) that se…

DNA ComplementaryTranscription GeneticAnnelidaMolecular Sequence DataChitinPeptideBioinformaticsBiochemistryEpitheliumBone morphogenetic protein 1Rapid amplification of cDNA endsSequence Analysis ProteinComplementary DNAbiology.animalAnimalsAmino Acid SequenceRNA MessengerCloning MolecularMolecular BiologyPeptide sequenceSea urchinChromatography High Pressure LiquidIn Situ Hybridizationchemistry.chemical_classificationMessenger RNABase SequenceSequence Homology Amino AcidbiologyReverse Transcriptase Polymerase Chain ReactionHelminth ProteinsSequence Analysis DNACell BiologyBlotting NorthernCUB domainProtein Structure TertiaryCell biologychemistryElectrophoresis Polyacrylamide GelEpidermisProtein BindingResearch ArticleBiochemical Journal
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Polish Yellow Sweet Clover (Melilotus officinalis L.) Honey, Chromatographic Fingerprints, and Chemical Markers

2017

A case study of Polish Melilotus officinalis honey was presented for the first time. Gas chromatography–mass spectrometry (GC-MS) (after steam distillation, Soxhlet extraction, ultrasonic solvent extraction, and solid phase extraction (SPE)) and targeted high performance liquid chromatography with a photodiode array detector (HPLC-PAD) were applied to determine the characteristic components of honey. While ubiquitous in most honeys, carbohydrates, terpene derivatives, and phenylacetic acid dominated in the Soxhlet extracts (25.54%) and in the application of SPE (13.04%). In addition, lumichrome (1.85%) was found, and may be considered as a marker of this honey. Due to the presence of these …

DPPHFlavonoidPharmaceutical Science01 natural sciencesHigh-performance liquid chromatographyvolatileAntioxidantsCatechinGas Chromatography-Mass SpectrometryArticleAnalytical Chemistrylaw.inventionlcsh:QD241-441Steam distillationchemistry.chemical_compound0404 agricultural biotechnologyPhenolslcsh:Organic chemistryMelilotus officinalislawGallic AcidDrug DiscoveryMedicagoHumansGallic acidSolid phase extractionPhysical and Theoretical ChemistryChromatography High Pressure LiquidFlavonoidschemistry.chemical_classificationChromatographybiology010401 analytical chemistryOrganic ChemistryExtraction (chemistry)honey markersHoney04 agricultural and veterinary sciencesbiology.organism_classificationMelilotus officinalis040401 food science0104 chemical sciencesyellow sweet cloverchemistryChemistry (miscellaneous)yellow sweet clover; <i>Melilotus officinalis</i>; phenolic; volatile; honey markersMolecular MedicinephenolicMolecules; Volume 22; Issue 1; Pages: 138
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Supported liquid membrane extraction with single hollow fiber for the analysis of fluoroquinolones from environmental surface water samples

2010

Abstract In this work, the simple analytical method for the determination of four fluoroquinolone antibiotics: ciprofloxacin, enrofloxacin, norfloxacin and danofloxacin, in environmental surface water samples is described. Sample pretreatment step was performed by the application of a technique based on supported liquid membrane extraction with the configuration of single hollow fiber (HF-SLM). The HPLC system with diode array detection was used for final analysis of studied analytes. Various parameters affecting the extraction efficiency during HF-SLM enrichment, such as type of membrane diluent, pH of donor (sample) and acceptor phases, as well as an enrichment time and salt content of sa…

DanofloxacinAnalytical chemistrySodium ChlorideBiochemistryHigh-performance liquid chromatographyDiluentSensitivity and SpecificityAnalytical ChemistryRiversmedicinehollow fiberenvironmental samplesSample preparationfluoroquinolonesChromatography High Pressure LiquidDetection limitChromatographysample preparationChemistryOrganic ChemistryExtraction (chemistry)Reproducibility of ResultsMembranes ArtificialGeneral MedicineHydrogen-Ion ConcentrationAnti-Bacterial Agentssupported liquid membrane extractionWater treatmentHydrochloric AcidEnrichment factorWater Pollutants Chemicalmedicine.drugJournal of Chromatography A
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High Pressure Liquid Chromatographic Analysis of Barbiturates in the Picomole Range by Fluorometry of Their DANS-Derivatives

1974

Dansyl CompoundsChromatographyRange (particle radiation)ChromatographyChemistryMicrochemistryAnalytical chemistryGeneral MedicineFluorescence spectroscopyAnalytical ChemistrySpectrometry FluorescenceHigh pressureBarbituratesMethodsPressureHumansJournal of Chromatographic Science
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A rapid separation of the four major deoxynucleosides and deoxyinosine by high-pressure liquid cation-exchange chromatography

1973

DeoxyribonucleasesChromatographyIon exchangePhosphoric Diester HydrolasesVenomsChemistryDeoxyribonucleotidesIon chromatographyBiophysicsPhosphoric Diester HydrolasesDeoxyribonucleosidesDNACell BiologyAlkaline PhosphataseChromatography Ion ExchangeBiochemistryMicrococcusHigh pressureMethodsPressureMolecular BiologyNucleic acid analogueAnalytical Biochemistry
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Specificity of deoxyribonuclease hydrolysis determined by high-performance liquid anion-exchange chromatography

1980

DeoxyribonucleasesChromatographyLymphomaIon exchangeChemistryOrganic ChemistryDeoxyribonucleaseDNANeoplasms ExperimentalGeneral MedicineChromatography Ion ExchangeBiochemistryCell LineAnalytical ChemistryDNA metabolismMiceHydrolysisBiochemistryAnimalsChromatography High Pressure LiquidJournal of Chromatography A
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An isocratic high-pressure liquid chromatographic purification method for radioactively labeled deoxyribonucleoside triphosphates.

1976

Abstract A method is described for the rapid purification of radioactively labeled deoxyribonucleoside tri­phosphates from their spontaneously emerging hydrolysis products deoxyribonucleoside diphosphate, deoxyribonucleoside monophosphate, and deoxyribonucleoside. The separations which are finished within 3 min or less are carried out on a 0.1X5 cm column filled with LiChrosorb-NH2 , using isocratic elution with 0.025 м potassium phosphate, pH 6 .8 , in a high-pressure liquid chromatograph at room temperature and a flow rate of 30 ml · h-1(flow velocity 63.7 cm·min-1).

Deoxyribonucleosidechemistry.chemical_compoundHydrolysisIsocratic elutionChromatographychemistryPotassium phosphateHigh pressureDeoxyribonucleotidesPurification methodsGeneral Biochemistry Genetics and Molecular BiologyChromatography High Pressure LiquidZeitschrift fur Naturforschung. Section C, Biosciences
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Analysis of LSD in human body fluids and hair samples applying ImmunElute columns.

2000

Immunoaffinity extraction units (LSD ImmunElute) are commercially available for the analysis of lysergic acid diethylamide (LSD) in urine. The ImmunElute resin contains immobilized monoclonal antibodies to LSD. We applied the ImmunElute procedure to serum and also to human hair samples. For hair analysis the samples were first extracted with methanol under sonication. The extracts were then purified using the ImmunElute resin. LSD analysis was carried out with HPLC and fluorescence detection. The immunoaffinity extraction provides highly purified extracts for chromatographic analysis. The limit of detection (signal-to-noise ratio = 3) has been determined to be < 50 pg regardless of which sa…

Detection limitAdultMaleChromatographyAdolescentChemistryIllicit DrugsSonicationHair analysisExtraction (chemistry)UrineHigh-performance liquid chromatographyChromatography AffinityPathology and Forensic MedicineBody FluidsSubstance Abuse DetectionLysergic Acid DiethylamideAffinity chromatographyHumansGas chromatography–mass spectrometryLawChromatography High Pressure LiquidHairForensic science international
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Liquid Chromatographic Analysis of Amphetamine and Related Compounds in Urine Using Solid-Phase Extraction and 3,5-Dinitrobenzoyl Chloride for Deriva…

1997

A chromatographic method for the analysis of amphetamine and related compounds in urine using 3,5-dinitrobenzoyl chloride (3,5-DNB) as a labeling reagent is presented. This assay is based on the employment of solid-phase extraction (SPE) cartridges for sample cleanup and derivatization. Experimental conditions are optimized for the simultaneous derivatization of ephedrine, norephedrine, pseudoephedrine, beta-phenylethylamine, amphetamine, methamphetamine, and 3-phenylpropylamine. The derivatives formed are separated in a LiChrospher 1000 RP18 (125 x 4-mm i.d., 5-microns film thickness) analytical column using a water-acetonitrile gradient elution and detected at 254 nm. Derivatization in C1…

Detection limitAnalyteChromatographyAmphetaminesGeneral MedicinePseudoephedrineHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryNitrobenzoatesReagentmedicineIndicators and ReagentsSolid phase extractionEphedrineDerivatizationChromatography High Pressure Liquidmedicine.drugJournal of Chromatographic Science
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Green determination of eight water-soluble B vitamins in cosmetic products by liquid chromatography with ultraviolet detection.

2021

Abstract B vitamins are a group of compounds with beneficious properties for dermatologic care, and therefore they are included in the cosmetic formulations as high added-value ingredients. In this paper, an analytical method for the simultaneous determination of eight water-soluble B vitamins in cosmetic products is reported for the first time. This method is based on liquid chromatography with ultraviolet detection (LC-UV) analysis after simple water leaching of the analytes from the cosmetic matrix. No organic solvents are required, beyond the ethanol used in the chromatographic mobile phase. The proposed method has been successfully validated showing good linearity, limits of detection …

Detection limitAnalyteChromatographyChemistryClinical BiochemistryPharmaceutical ScienceReproducibility of ResultsWaterRepeatabilityCosmeticsmedicine.disease_causeAnalytical ChemistryMatrix (chemical analysis)B vitaminsWater solubleLeaching (chemistry)Drug DiscoveryVitamin B ComplexmedicineSolventsSpectroscopyUltravioletChromatography High Pressure LiquidChromatography LiquidJournal of pharmaceutical and biomedical analysis
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