Search results for "CENTRIFUGE"

showing 10 items of 30 documents

Comparison of quantum dot-binding protein tags: Affinity determination by ultracentrifugation and FRET

2013

Abstract Background Hybrid complexes of proteins and colloidal semiconductor nanocrystals (quantum dots, QDs) are of increasing interest in various fields of biochemistry and biomedicine, for instance for biolabeling or drug transport. The usefulness of protein–QD complexes for such applications is dependent on the binding specificity and strength of the components. Often the binding properties of these components are difficult and time consuming to assess. Methods In this work we characterized the interaction between recombinant light harvesting chlorophyll a / b complex (LHCII) and CdTe/CdSe/ZnS QDs by using ultracentrifugation and fluorescence resonance energy transfer (FRET) assay exper…

ChemistryBinding proteinBiophysicsNanoparticleProtein tagBiochemistryCrystallographyB vitaminsFörster resonance energy transferQuantum dotQuantum DotsFluorescence Resonance Energy TransferNanoparticlesUltracentrifugeChlorophyll Binding ProteinsUltracentrifugationMolecular BiologyBinding selectivityProtein BindingBiochimica et Biophysica Acta (BBA) - General Subjects
researchProduct

Preparation of Native and Recombinant Light-Harvesting Chlorophyll-<I>a/b </I>Complex

2004

Procedures to isolate native light-harvesting chlorophyll-a/b complex (LHCIIb) and to reconstitute recombinant LHCIIb are described. Separation of trimeric from monomeric forms and free pigment by sucrose density-gradient ultracentrifugation can be applied to both native and reconstituted complexes. The preparations are characterized by their pigment composition, protein pattern, and spectral properties.

Chlorophyll aSucrosePigment compositionlaw.inventionchemistry.chemical_compoundB vitaminsPigmentMonomerchemistryBiochemistrylawvisual_artRecombinant DNAvisual_art.visual_art_mediumUltracentrifuge
researchProduct

A Classical Synthesis of the Collagen-like Peptides with the Sequence Z(GlyProPro)nOBut and their characterization with circular dichroism and ultrac…

1975

Oligopeptides with the sequence Z(GlyProPro)nOBut (n = 3–7) were synthesized along a clasical pathway. Generally long fragments were condensed in order to allow an easy separation of the products from the reactants. It is established by molecular weight determination and measurements of circular dichroism that the peptides form the collagen-like triple helix in methanol and that they assume the random coil conformation in dilute acetic acid. The circular dichroism spectra agree reasonably well with the corresponding spectra for (ProProGly)10 which was obtained by solid phase synthesis in another laboratory.

Circular dichroismCircular DichroismOrganic ChemistrySequence (biology)BiochemistryCatalysisRandom coilSpectral lineInorganic ChemistryAcetic acidchemistry.chemical_compoundCrystallographySolid-phase synthesischemistryDrug DiscoveryAmino Acid SequenceCollagenUltracentrifugePhysical and Theoretical ChemistryOligopeptidesUltracentrifugationTriple helixHelvetica Chimica Acta
researchProduct

Numerical analysis of density gradient centrifugation profiles from eukaryotic DNA

1990

A numerical method for the deconvolution of superimposed Gaussian distributions with a unique solution has been proposed by Medgyessy [10]. We have tested the usefulness of this method for the analysis of density gradient centrifugation profiles from eukaryotic DNA, which are normally composed from overlapping Gaussian distributed profiles of several subcomponents with different mean buoyant densities. From the analysis of human DNA and from model calculations we conclude that major subcomponents can be identified by this method, if they differ in their buoyant density by approximatly 0.005 g/ml. Minor components can only be identified if the total DNA has been fractionated according to buo…

Differential centrifugationPolymers and PlasticsChemistryGaussianNumerical analysisAnalytical chemistryBuoyant densityEukaryotic DNA replicationsymbols.namesakechemistry.chemical_compoundColloid and Surface ChemistryMaterials ChemistrysymbolsUltracentrifugeDeconvolutionPhysical and Theoretical ChemistryBiological systemDNAColloid & Polymer Science
researchProduct

Ultracentrifugation studies on the native form of the first component of human complement (C1)

1976

Dose-Response Relationship DrugChemistryBiophysicsCell BiologyComplement System ProteinsBiochemistryComplement (complexity)SolutionsStructure-Activity RelationshipBiochemistryStructural BiologyComplement C1Component (UML)GeneticsHumansUltracentrifugeMolecular BiologyUltracentrifugationFEBS Letters
researchProduct

Distribution of chlorpromazine in a simplified blood influenced by various drugs

1973

The binding of chlorpromazine to erythrocytes and to albumin as influenced by other drugs was studied in a simplified blood (31.5±0.3% bovine erythrocytes, 4 g-% bovine serum albumin in 0.02 M phosphate buffer solution containing 0.15 M NaCl). the total concentration of chlorpromazine in the simplified blood was 10−4 M, the concentration of the displacing drugs was 10−3 M. After an incubation period of 3 h at 22° C the chlorpromazine concentration was determined in the albumin solution after centrifugation of the blood at 3000×g and in the aqueous phase after ultracentrifugation at 150000×g. Under control conditions 68.1±0.9% of chlorpromazine was bound to the erythrocytes, 28.5±0.9% was bo…

ErythrocytesChlorpromazineIndomethacinSuraminBenzoatesBinding CompetitiveIncubation periodCoumarinsmedicineAnimalsDistribution (pharmacology)CentrifugationThiopentalBovine serum albuminChlorpromazinePharmacologySulfonamidesBinding SitesChromatographyQuininebiologyProbenecidChemistryFatty AcidsAqueous two-phase systemAlbuminSerum Albumin BovineGeneral MedicineChlorothiazideTetracyclineAntidepressive AgentsSalicylatesAcetazolamidePhenylbutazoneSolubilityPhenytoinbiology.proteinCattleUltracentrifugeDeoxycholic AcidProtein Bindingmedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
researchProduct

Physicochemical characterization of the fifth (C5), sixth (C6), seventh (C7), eighth (C8) and ninth (C9) component of guinea pig complement.

1971

A physicochemical characterization of the purified guinea pig complement components C5 to C9 is given. For this purpose the sedimentation rate, the diffusion coefficient, the molecular weight and the isoelectric point were determined and compared with the values already known for the guinea pig and human complement system. For the determination of the physicochemical parameters gel filtration on Sephadex G-200, ultracentrifugation applying a sucrose density gradient and thin-layer isoelectric focusing were used. By comparing the values of the human and guinea pig complement a remarkable similarity is shown.

ErythrocytesDensity gradientChemical PhenomenaImmunologySize-exclusion chromatographyGuinea PigsBiologyGuinea pigHemoglobinsCentrifugation Density GradientImmunology and AllergyAnimalsHumansChromatographyIsoelectric focusingChemistry PhysicalVenomsElectric ConductivitySnakesComplement System ProteinsCatalaseComplement systemMolecular WeightIsoelectric pointSephadexImmunoglobulin GImmunologyChromatography GelUltracentrifugeIsoelectric FocusingEuropean journal of immunology
researchProduct

ATR-FTIR spectroscopy for the routine quality control of exosome isolations

2021

Abstract Exosomes are nanosized vesicles containing specific cargos of DNA, RNA, proteins, metabolites, and intracellular and membrane lipids. Exosome isolation needs to be optimized carefully depending on the type of biofluid and tissue and the retrieved exosomes need to be characterized. The main objective of this study was to determine the feasibility of a multimodal analysis of Attenuated Total Reflectance – Fourier Transform Infrared (ATR-FTIR) spectroscopy and UPLC–QqTOF-MSMS for the development of a routine quality control tool of isolated exosomes and the rapid characterization of their lipid profiles and total protein content. Using human milk as model example, exosomes were isolat…

Fourier transform infrared (ATR-FTIR)Membrane lipidsOmicsExosomes01 natural sciencesExosomeAnalytical Chemistry03 medical and health sciencesstomatognathic systemMETLINSpectroscopy030304 developmental biology0303 health sciencesChemistryProcess Chemistry and TechnologyVesicleHuman milk010401 analytical chemistryExtracellular vesiclesSphingolipidMicrovesicles0104 chemical sciencesComputer Science ApplicationsBiochemistryAttenuated total reflectionLipidomicslipids (amino acids peptides and proteins)UltracentrifugeAttenuated total reflectanceSoftwareChemometrics and Intelligent Laboratory Systems
researchProduct

Field-free two-direction alignment alternation of linear molecules by elliptic laser pulses

2005

We show that a linear molecule subjected to a short specific elliptically polarized laser field yields postpulse revivals exhibiting alignment alternatively located along the orthogonal axis and the major axis of the ellipse. The effect is experimentally demonstrated by measuring the optical Kerr effect along two different axes. The conditions ensuring an optimal field-free alternation of high alignments along both directions are derived.

Kerr effectI-2 MOLECULESField (physics)General Physics and AstronomyFOS: Physical sciencesLinear molecular geometry02 engineering and technologyElliptical polarizationEllipse01 natural scienceslaw.inventionOpticsREVIVAL STRUCTURESlaw0103 physical sciencesOPTICAL CENTRIFUGEAlternation (formal language theory)010306 general physicsPhysicsQuantum Physicsbusiness.industry021001 nanoscience & nanotechnologyLaserOrthogonal coordinates0210 nano-technologybusinessQuantum Physics (quant-ph)
researchProduct

Rapid Radiochemical Separation Procedures from Aqueous Solutions

1992

The state-of-the-art in the field of rapid radiochemical separation procedures is illustrated by two systems using aqueous solutions as input: ARCA, an apparatus for repetitive separations, and SISAK, a centrifuge system for continuous separations. Applications presented are: Solvent extraction of element 105 investigated with 34-s 262105 using ARCA, and decay scheme studies of the fission product 1.0-s 110Tc by means of SISAK.

Nuclear fission productCentrifugeAqueous solutionDecay schemeChromatographyChemistrySolvent extraction
researchProduct