Search results for "Molecular weight"

showing 10 items of 366 documents

Territorial localization of heat shock mRNA production in sea urchin gastrulae.

1985

In situ hybridization experiments with a labeled DNA probe indicate that the ability to respond to heat shock with the production of the mRNA for the 70 kd heat shock protein is segregated into the ectodermal cells already at the gastrula stage or earlier during the embryonic development of Paracentrotus lividus.

animal structuresIn situ hybridizationParacentrotus lividusbiology.animalEctodermmedicineAnimalsRNA MessengerSea urchinHeat-Shock ProteinsMessenger RNAbiologyHybridization probeEmbryogenesisNucleic Acid HybridizationCell BiologyAnatomyGastrulabiology.organism_classificationCell biologyGastrulationMolecular WeightShock (circulatory)Sea Urchinsembryonic structuresAutoradiographymedicine.symptomCell biology international reports
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Elimination and distribution of different substituted phenols by frog (Rana temporaria) and crayfish (Astacus leptodactylus)

1981

biologyHealth Toxicology and MutagenesisRana temporariaZoologyAstacoideaGeneral MedicineToxicologyCrayfishAstacus leptodactylusbiology.organism_classificationPollutionRanaMolecular WeightKineticschemistry.chemical_compoundPhenolschemistryGoldfishAnimalsTissue DistributionPhenolsBulletin of Environmental Contamination and Toxicology
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Electron microscopy and biochemical characterization of a 350-kDa annular hemolymph protein from the keyhole limpet Megathura crenulata

1994

The isolation and biochemical characterization of an annular non-hemocyanin hemolymph protein from a marine gastropod, the Californian giant keyhole limpet (Megathura crenulata) is presented. By analytical ultracentrifugation, the protein has a sedimentation coefficient of 12S and molecular mass of approximately 350 kDa. The subunit mass, obtained by SDS/PAGE in the presence of -SH reagent and 8 M urea, is approximately 35 kDa, thereby indicating the presence of 10 subunits in the native molecule. By negative staining, the protein is revealed in one predominant image projection as a pentagonal approximately 8 nm ring-like structure with an approximately 2-nm stain-filled centre and, in anot…

biologyMolecular massProtein Conformationmedicine.medical_treatmentProtein subunitLimpetProteinsHemocyaninMegathura crenulatabiology.organism_classificationBiochemistryNegative stainMolecular WeightMicroscopy ElectronCrystallographyMolluscaHemolymphLimulusHemolymphmedicineBiophysicsAnimalsElectrophoresis Polyacrylamide GelUltracentrifugationEuropean Journal of Biochemistry
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Effect of hydrogen on the ethylene polymerization process over Ziegler–Natta catalysts supported on MgCl2(THF)2. I. Studies of the chain‐transfer rea…

2001

The effect of hydrogen on the molecular weight of polyethylene obtained over vanadium catalysts (based on VCl4 and VOCl3) supported on MgCl2(THF)2 was studied and the results were compared to those obtained for similar titanium catalysts. It was confirmed that the dependencies of the transfer reaction on the hydrogen concentration are a half‐order in all investigated systems. However, the transition metal of the catalytic site affects the ratio of the transfer rate with hydrogen to the propagation rate (ktr,H/kp) and the results showed that hydrogen is a more effective agent of polyethylene molecular weight control in vanadium‐based systems as compared to the titanium catalyst.

chain transfer with hydrogenvanadium and titanium catalystshydrogenmolecular weightethylene polymerizationJournal of Applied Polymer Science
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Influence of Polymer Molecular Weight on Drug–polymer Solubility: A Comparison between Experimentally Determined Solubility in PVP and Prediction Der…

2015

ABSTRACT: In this study, the influence of polymer molecular weight on drug–polymer solubility was investigated using binary systems containing indomethacin (IMC) and polyvinylpyrrolidone (PVP) of different molecular weights. The experimental solubility in PVP, measured using a differential scanning calorimetry annealing method, was compared with the solubility calculated from the solubility of the drug in the liquid analogue N-vinylpyrrolidone (NVP). The experimental solubility of IMC in the low-molecular-weight PVP K12 was not significantly different from that in the higher molecular weight PVPs (K25, K30, and K90). The calculated solubilities derived from the solubility in NVP (0.31–0.32 …

chemistry.chemical_classificationCalorimetry Differential ScanningPolyvinylpyrrolidonePolymersIndomethacinPovidonePharmaceutical SciencePolymerFlory–Huggins solution theoryPyrrolidinonesMolecular Weightchemistry.chemical_compoundHildebrand solubility parameterMonomerDifferential scanning calorimetrySolubilitychemistryChemical engineeringSpray dryingmedicineOrganic chemistrySolubilitymedicine.drugJournal of Pharmaceutical Sciences
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A fast method for determining low-molecular-mass aliphatic carboxylic acids by high-performance liquid chromatography–atmospheric pressure chemical i…

2006

A fast quantitative high-performance liquid chromatographic separation method with atmospheric pressure chemical ionization mass spectrometric detection (HPLC-APCI-MS) was developed for the determination of low-molecular-mass aliphatic mono- and dicarboxylic acids typically present in different industrial process waters. A mixture of glycolic, lactic, a-glucoisosaccharinic, oxalic, maleic, fumaric, succinic, malic, glutaric, methylsuccinic, and adipic acids was separated using an RP chromatographic system. Adipic acid was used as an internal standard to calculate correlation coefficients for the acids studied. The chromatographic analysis of these acids was primarily carried out by means of…

chemistry.chemical_classificationChemical ionizationAdipic acidChromatographyFormic acidCarboxylic acidCarboxylic AcidsFiltration and SeparationAtmospheric-pressure chemical ionizationHigh-performance liquid chromatographyMass SpectrometryAnalytical ChemistryMolecular Weightchemistry.chemical_compoundAtmospheric PressureDicarboxylic acidchemistryLiquid chromatography–mass spectrometryChromatography High Pressure LiquidJournal of Separation Science
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Isolation and characterization of a chlorogenic acid esterase from Aspergillus niger.

1980

Abstract The isolation and characterization of a specific chlorogenic acid esterase is described. The enzyme activity is measured by determination of the hydrolysis product caffeic acid. The enzyme had been concentrated by means of ultrafiltration and column-chromatography. The pH- and temperature optimum were 6.5 and 45 °C respectively. Divalent cations were not required for the enzyme activity. As other esterases, this enzyme is inhibited by di-isopropyl-phosphorofluoridate. The Km-value is 0.70 mᴍ chlorogenic acid, the molecular weight 240000. The described enzyme is specific for chlorogenic acid. On the other hand a typical unspecific esterase like the pig liver esterases does not split…

chemistry.chemical_classificationChromatographybiologyIsoelectric focusingSwineAspergillus nigerbiology.organism_classificationEsteraseGeneral Biochemistry Genetics and Molecular BiologyEnzyme assayIsoenzymesMolecular Weightchemistry.chemical_compoundHydrolysisKineticsEnzymeChlorogenic acidchemistryLiverCaffeic acidbiology.proteinAnimalsAspergillus nigerCarboxylic Ester HydrolasesZeitschrift fur Naturforschung. Section C, Biosciences
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Purification of rat liver epoxide hydratase to apparent homogeneity.

1975

Epoxide hydratase (EC 4.2.1.63) is a microsomal enzyme which catalyses the conversion of epoxides to trans-dihydrodiols. Epoxides, produced by the action of microsomal monooxygenases (EC 1.14.1.1) from aromatic and olefinic compounds, are thought to be responsible for many of the harinful effects of polycyclic hydrocarbons and related compounds. Thus epoxide hydratase, together with glutathione 9transferases, (EC 2.5.1.18) may play an important role in the removal of carcinogenic and cytotoxic metabolites (for reviews see [l-3]). It has been reported [4,5] that dihydrodiols formed from some polycyclic hydrocarbons (benz(a)anthracene and benzo(a)pyrene) are reactivated by the microsomal mono…

chemistry.chemical_classificationEpoxide HydrolasesMaleAnthraceneBiophysicsCell BiologyGlutathioneMonooxygenaseBiochemistryRatsMolecular Weightchemistry.chemical_compoundEnzymechemistryBiochemistryStructural BiologyGeneticsMicrosomeMicrosomes LiverPyreneAnimalsPolycyclic HydrocarbonsMolecular BiologyCarcinogenHydro-LyasesFEBS letters
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Biochemical characterization of two functional human liver acyl-CoA oxidase isoforms 1a and 1b encoded by a single gene

2007

Abstract Human acyl-CoA oxidase 1 (ACOX1) is a rate-limiting enzyme in peroxisomal fatty acids β-oxidation and its deficiency is associated with a lethal, autosomal recessive disease, called pseudoneonatal-adrenoleukodystrophy. Two mRNA variants, transcribed from a single gene encode ACOX1a or ACOX1b isoforms, respectively. Recently, a mutation in a splice site has been reported [H. Rosewich, H.R. Waterham, R.J. Wanders, S. Ferdinandusse, M. Henneke, D. Hunneman, J. Gartner, Pitfall in metabolic screening in a patient with fatal peroxisomal β-oxidation defect, Neuropediatrics 37 (2006) 95–98.], which results in the defective peroxisomal fatty acids β-oxidation. Here, we show that these mRNA…

chemistry.chemical_classificationGene isoformOxidase testBiophysicsCell BiologyBiologyPeroxisomeBiochemistryIsozymeMolecular biologyArticleEnzyme ActivationIsoenzymesMolecular WeightEnzymechemistryBiochemistryLiverEnzyme StabilityAcyl-CoA oxidaseACOX1HumansHeterologous expressionAcyl-CoA OxidaseMolecular Biology
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Calculation of the molecular masses of two newly synthesized thermostable enzymes isolated from thermophilic microorganisms

1995

Two thermostable enzymes synthesized by thermophilic microorganisms were isolated and purified. A thermostable beta-galactosidase was produced in a continuous fermentation process by Bacillus stearothermophilus TP 32 as an intracellular enzyme. After applying different concentration procedures the raw extract enzyme was prepurified on a Sephadex G-200 size exclusion column. The isolated beta-galactosidase fraction was then separated with HPLC on a TSK G 3000 SW size exclusion column to determine the molecular mass based on calibration curves of standard proteins. The other enzyme, a thermostable protease, was synthesized by Bacillus stearothermophilus TP 26 as an extracellular enzyme. After…

chemistry.chemical_classificationHot TemperatureProteaseChromatographybiologyMolecular massmedicine.medical_treatmentThermophileSize-exclusion chromatographyGeneral Chemistrybeta-Galactosidasebiology.organism_classificationBacillalesHigh-performance liquid chromatographyGeobacillus stearothermophilusMolecular WeightEnzymechemistrySephadexEndopeptidasesEnzyme StabilityChromatography GelmedicineChromatography High Pressure LiquidJournal of Chromatography B: Biomedical Sciences and Applications
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