Search results for " LAB"

showing 10 items of 2393 documents

Il laboratorio di chimica

2001

Chimica laboratorio
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Filling the “green gap” of the major light-harvesting chlorophyll a/b complex by covalent attachment of Rhodamine Red

2009

AbstractThe major light-harvesting chlorophyll a/b complex (LHCII) greatly enhances the efficiency of photosynthesis in green plants. Recombinant LHCII can be assembled in vitro from its denatured, bacterially expressed apoprotein and plant pigments. This makes it an interesting candidate for biomimetic light-harvesting in photovoltaic applications. Due to its almost 20 pigments bound per apoprotein, LHCII absorbs efficiently in the blue and red spectral domains of visible light but less efficiently in the green domain, the so-called “green gap” in its absorption spectrum. Here we present a hybrid complex of recombinant LHCII with organic dyes that add to LHCII absorption in the green spect…

ChlorophyllLHCIIProtein FoldingFRET (Förster resonance energy transfer)Chlorophyll aAbsorption spectroscopyBiophysicsPhotosynthesisPhotochemistryBiochemistryRhodamineLight-harvesting complexchemistry.chemical_compoundPhotosynthesisFluorescent DyesRhodaminesChlorophyll Afood and beveragesSite-specific labelingCell BiologyMaleimide dyeB vitaminsSolar spectrumchemistryChlorophyllVisible spectrumBiochimica et Biophysica Acta (BBA) - Bioenergetics
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Localization of the N-terminal Domain in Light-harvesting Chlorophyll a/b Protein by EPR Measurements

2005

The conformational distribution of the N-terminal domain of the major light-harvesting chlorophyll a/b protein (LHCIIb) has been characterized by electron-electron double resonance yielding distances between spin labels placed in various domains of the protein. Distance distributions involving residue 3 near the N terminus turned out to be bimodal, revealing that this domain, which is involved in regulatory functions such as balancing the energy flow through photosystems (PS) I and II, exists in at least two conformational states. Models of the conformational sub-ensembles were generated on the basis of experimental distance restraints from measurements on LHCIIb monomers and then checked f…

ChlorophyllModels MolecularThreonineConformational changeTime FactorsLightMacromolecular SubstancesProtein ConformationPhotosynthetic Reaction Center Complex ProteinsLight-Harvesting Protein ComplexesElectronsTrimerCrystallography X-RayThylakoidsBiochemistryProtein Structure Secondarylaw.inventionResidue (chemistry)chemistry.chemical_compoundlawEscherichia coliAnimalsPhosphorylationAnnexin A4Electron paramagnetic resonanceMolecular BiologyPhotosystemPhotosystem I Protein ComplexChemistryChlorophyll AElectron Spin Resonance SpectroscopyPeasPhotosystem II Protein ComplexCell BiologyRecombinant ProteinsProtein Structure TertiaryOxygenN-terminusCrystallographyMonomerThylakoidMutationCattleSpin LabelsDimerizationJournal of Biological Chemistry
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Response to long-term NaHCO3-derived alkalinity in model Lotus japonicus Ecotypes Gifu B-129 and Miyakojima MG-20: transcriptomic profiling and physi…

2014

The current knowledge regarding transcriptomic changes induced by alkalinity on plants is scarce and limited to studieswhere plants were subjected to the alkaline salt for periods not longer than 48 h, so there is no information availableregarding the regulation of genes involved in the generation of a new homeostatic cellular condition after long-termalkaline stress.Lotus japonicusis a model legume broadly used to study many important physiological processes includingbiotic interactions and biotic and abiotic stresses. In the present study, we characterized phenotipically the response toalkaline stress of the most widely usedL. japonicusecotypes, Gifu B-129 and MG-20, and analyzed global t…

ChlorophyllOtras Biotecnología AgropecuariaPhysiologyApplied MicrobiologyPlant SciencePathogenesisPathology and Laboratory MedicinePlant RootsBiochemistryTranscriptomeZINCchemistry.chemical_compoundPlant MicrobiologyGene Expression Regulation PlantABIOTIC STRESSMETAL TRANSPORTERSMedicine and Health SciencesOligonucleotide Array Sequence AnalysisLOTUS JAPONICUSPlant Growth and DevelopmentMultidisciplinarybiologyEcotypePlant BiochemistryIRONQRMicrobial Growth and Development//purl.org/becyt/ford/4.4 [https]food and beveragesPlantsZincPlant PhysiologyShootHost-Pathogen InteractionsMedicineAntacidsAnatomymicroarrayPlant ShootsResearch ArticleBiotechnologyHistologyScienceIronPlant Cell BiologyLotus japonicusBiotecnología AgropecuariaalkalinityMycologyReal-Time Polymerase Chain ReactionResearch and Analysis MethodsMicrobiologyModel OrganismsIsoflavonoidSpecies SpecificityPlant and Algal ModelsBotanyAbiotic stressGene Expression ProfilingfungiOrganismsFungiBiology and Life SciencesPlant TranspirationCell Biologybiology.organism_classificationMICROARRAYSGene expression profilingSodium BicarbonatechemistryCIENCIAS AGRÍCOLASChlorophyllLotusPhysiological Processes//purl.org/becyt/ford/4 [https]Developmental BiologyPloS one
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Effects of dietary vitamin D3 administration on innate immune response of sea bass (Dicentrarchus labrax)

2014

Cholecalciferol Innate immunity Serum Leucocytes Sea bass (Dicentrarchus labrax L.) Teleost
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Analysis of trichothecenes in laboratory rat feed by gas chromatography-tandem mass spectrometry

2015

A method for the determination of seven trichothecenes, neosolaniol (NEO), diacetoxyscirpenol (DAS), deoxynivalenol (DON), nivalenol (NIV), fusarenon-X (FUS-X), 3-acetyldeoxynivalenol (3-ADON) and 15-acetyldeoxynivalenol (15-ADON), in laboratory rat feed by GC-MS/MS was developed. Sample extraction and purification was performed by an acidified mixture of acetonitrile/water (80-20% v/v). Limits of quantitation (LOQs) were between 1 and 10 μg kg(-1) for all studied trichothecenes. Eight concentration levels between the LOQ and 100 × LOQ were used for the calibration curves. Matrix-matched calibration was used for quantitation purposes to compensate the detector signal enhancement obtained fo…

Chromatography GasCalibration curveAnimal feedHealth Toxicology and MutagenesisTrichotheceneToxicologyTandem mass spectrometryDiacetoxyscirpenolchemistry.chemical_compoundTandem Mass SpectrometryAnimals LaboratoryAnimalsMycotoxinChromatographyGas Chromatography/Tandem Mass SpectrometryPublic Health Environmental and Occupational HealthGeneral ChemistryGeneral MedicineAnimal FeedRatschemistryGas chromatographyLaboratoriesTrichothecenesFood AnalysisFood ScienceFood Additives & Contaminants: Part A
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Processing of Generator-Produced 68Ga for Medical Application

2007

The (68)Ge/(68)Ga generator provides an excellent source of positron-emitting (68)Ga. However, newly available "ionic" (68)Ge/(68)Ga radionuclide generators are not necessarily optimized for the synthesis of (68)Ga-labeled radiopharmaceuticals. The eluates have rather large volumes, a high concentration of H(+) (pH of 1), a breakthrough of (68)Ge, increasing with time or frequency of use, and impurities such as stable Zn(II) generated by the decay of (68)Ga, Ti(IV) as a constituent of the column material, and Fe(III) as a general impurity.We have developed an efficient route for the processing of generator-derived (68)Ga eluates, including the labeling and purification of biomolecules. Prec…

ChromatographyAqueous solutionElutionIon chromatographyGallium RadioisotopesFraction (chemistry)Hydrochloric acidEquipment DesignReference StandardsEquipment Failure Analysischemistry.chemical_compoundColumn chromatographychemistryGermanyIsotope LabelingAcetoneRadiology Nuclear Medicine and imagingRadionuclide GeneratorJournal of Nuclear Medicine
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Partial least squares attenuated total reflectance IR spectroscopy versus chromatography: the greener method

2012

Method election is a complex task that must be done carefully in order to ensure the capability of analytical methodologies to provide appropriate data for problem solving. This is a real challenge in all fields, but especially with bioanalysis, which in many cases involves the need to do a large number of determinations in complex

ChromatographyBioanalysisChromatographyChemistryClinical BiochemistryInfrared spectroscopyGreen Chemistry TechnologyGeneral MedicineAnalytical ChemistryMedical Laboratory TechnologyAttenuated total reflectionSpectroscopy Fourier Transform InfraredPartial least squares regressionLeast-Squares AnalysisGeneral Pharmacology Toxicology and PharmaceuticsBioanalysis
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Ultra-high-pressure liquid chromatography tandem mass spectrometry method for the determination of 9 organophosphate flame retardants in water samples

2016

Few methods are available for comprehensive organophosphate flame retardants (PFRs) detection in water and wastewater. Gas chromatography has been employed previously, but this approach is less selective, not amenable for use with deuterated standards and can suffer unfavorable fragmentation. Ultra-high-pressure liquid chromatography tandem mass spectrometry (UHPLC-QqQ-MS/MS) has become the most promising platform, already applied successfully for analysis of selected PFRs in some environmental matrices like water and wastewater. However, the presence of some interferences from the dissolvent, the equipment and the used materials should be taken into account. The procedure involves: The fir…

ChromatographyChemistry010401 analytical chemistryClinical BiochemistryAnalytical chemistryAnalysis of organophosphate flame retardants in water by SPE and UHPLC–MS/MS using a trap column.solid phase extractionWater010501 environmental sciences01 natural sciencesTrap column0104 chemical sciencesOrganophosphate flame retardantsMedical Laboratory TechnologyWastewaterLC–MS/MSLiquid chromatography–mass spectrometryInterferencesLc ms msEnvironmental ScienceGas chromatographyUltra high pressureSolid phase extraction0105 earth and related environmental sciencesComputingMethodologies_COMPUTERGRAPHICSMethodsX
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Staining mitochondria in Saccharomyces cerevisiae.

1969

After testing various procedures (amidoblack 10B, acid fuchsin-methyl blue, Luxol fast blue MBS-phloxine, toluidine blue O, Jams green B and pinacyanol), three stains can be recommended for staining both types of mitochondria (globose and threadlike) in the cells of Saccharomyces cerevisiae: (1) 0.1% solution of amidoblack 10B in citrate buffer (pH 3.0) for 10 min; (2) 0.01% solution of toluidine blue O in phosphate buffer (pH 6.0) for 30 min; (3) 0.01% solution of Janus green B in distilled water (pH 5.6) for 30 min. The latter stain is most specific because its staining reaction depends upon the action of the mitochondrial enzyme cytochrome c oxidase. Yet, low concentrations and short inc…

ChromatographyTime FactorsStaining and LabelingJanus Green BSaccharomyces cerevisiaeBiologyBuffersHydrogen-Ion Concentrationbiology.organism_classificationStainLuxol fast blue stainStainingMitochondriaElectron Transport Complex IVchemistry.chemical_compoundSaccharomyceschemistryBiochemistryDistilled waterbiology.proteinMethodsCytochrome c oxidaseAnatomyColoring AgentsIncubationStain technology
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