Search results for "centrifugation"

showing 10 items of 124 documents

Univacuolar refractile hemocytes from the tunicate Ciona intestinalis are cytotoxic for mammalian erythrocytes in vitro

1996

A discontinuous, Percoll density gradient was used to separate hemocyte populations from the hemolymph of Ciona intestinalis. Hemocytes from each band were examined for their frequency, morphology, and cytotoxic activity against rabbit and sheep erythrocytes; results were expressed as a percentage of hemolysis. Statistical analysis revealed that only the "univacuolar" granulocytes from Band 5, which contain a vacuole of refractile material, were cytotoxic. Cytotoxic activity was inhibited by sphingomyelin. For the first time in tunicates, lytic activity against erythrocytes was assessed by an assay based on plaque-forming cells. Plaques of lysis were revealed against rabbit erythrocytes but…

HemocytesHemolytic Plaque TechniqueVacuoleCell SeparationHemolysisHemolytic Plaque TechniqueHemolysin ProteinsHemolymphHemolymphmedicineCentrifugation Density GradientCytotoxic T cellAnimalsCiona intestinalisSheepbiologybiology.organism_classificationmedicine.diseaseMolecular biologyHemolysisTunicateCiona intestinalisSphingomyelinsImmunologyRabbitsGeneral Agricultural and Biological SciencesPercoll
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A homemade cytospin apparatus

2006

Information retrievalStaining and LabelingChemistryCytospin apparatusBiophysicsCentrifugationCell BiologyCell SeparationEquipment DesignMolecular BiologyBiochemistryBody Fluids
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Improving extracellular vesicles visualization: From static to motion

2020

AbstractIn the last decade, extracellular vesicles (EVs) have become a hot topic. The findings on EVs content and effects have made them a major field of interest in cancer research. EVs, are able to be internalized through integrins expressed in parental cells, in a tissue specific manner, as a key step of cancer progression and pre-metastatic niche formation. However, this specificity might lead to new opportunities in cancer treatment by using EVs as devices for drug delivery. For future applications of EVs in cancer, improved protocols and methods for EVs isolation and visualization are required. Our group has put efforts on developing a protocol able to track the EVs for in vivo intern…

InteractionIntravital MicroscopyComputer sciencemedia_common.quotation_subjectlcsh:MedicineAntineoplastic AgentsvideoExosomesNSCLCTime-Lapse ImagingExtracellular vesiclesArticleFluorescence imagingExtracellular VesiclesSettore BIO/13 - Biologia ApplicataCell Line TumorNeoplasmsmedicineHumansTissue specificInternalizationlcsh:ScienceBiologymedia_commonDrug CarriersMicroscopy ConfocalMultivesicular bodiesMultidisciplinaryDisease progressionlcsh:RCancerEpithelial Cellsmedicine.diseaseCancer treatmentCell biologyinternalizationNucleic acidsConfocal microscopyTransportersDrug deliveryDisease ProgressionMicroscopy Electron ScanningIsolation separation and purificationlcsh:QHuman medicineextracellular vesicleEngineering sciences. TechnologyUltracentrifugation
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Calcium-Dependent Assembly of Centrin-G-Protein Complex in Photoreceptor Cells

2002

Photoexcitation of rhodopsin activates a heterotrimeric G-protein cascade leading to cyclic GMP hydrolysis in vertebrate photoreceptors. Light-induced exchanges of the visual G-protein transducin between the outer and inner segment of rod photoreceptors occur through the narrow connecting cilium. Here we demonstrate that transducin colocalizes with the Ca(2+)-binding protein centrin 1 in a specific domain of this cilium. Coimmunoprecipitation, centrifugation, centrin overlay, size exclusion chromatography, and kinetic light-scattering experiments indicate that Ca(2+)-activated centrin 1 binds with high affinity and specificity to transducin. The assembly of centrin-G-protein complex is medi…

Lightgenetic structuresChromosomal Proteins Non-HistoneMacromolecular SubstancesImmunoprecipitationG proteinCentrifugationPlasma protein bindingBiologyRetinaSubstrate SpecificityRats Sprague-DawleyMiceHeterotrimeric G proteinCalcium-binding proteinAnimalsScattering RadiationTransducinMicroscopy ImmunoelectronCell Growth and DevelopmentMolecular BiologyCalcium-Binding ProteinsCell BiologyHeterotrimeric GTP-Binding ProteinsPrecipitin TestsRatsCell biologyMice Inbred C57BLMolecular WeightRhodopsinCentrinChromatography Gelbiology.proteinCalciumCattlesense organsTransducinPhotoreceptor Cells VertebrateProtein BindingSignal TransductionMolecular and Cellular Biology
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Centrifugation does not alter spatial distribution of `BEP4' mRNA in paracentrotus lividus EGG

1997

AbstractParacentrotus lividus unfertilized eggs were centrifuged in a sucrose gradient, so to split each into two parts: a nucleated light fragment and an anucleated heavy fragment. Northern blot analyses utilizing a bep4 probe as animal marker and H2A histone gene and 12S-mit RNA as controls indicate that the eggs are elongated along the animal-vegetal axis during centrifugation and thereafter split into an animal and a vegetal half. Treatment of the eggs with colchicine before centrifugation abolishes the animal localization of bep4 mRNA.

Localized mRNABiophysicsCentrifugationCell FractionationBiochemistryMicrotubulesParacentrotus lividuschemistry.chemical_compoundStructural BiologyBotanyA/V axisGeneticsCentrifugation Density GradientColchicineAnimalsCentrifugationNorthern blotRNA MessengerMolecular BiologyGeneIn Situ HybridizationOvumMessenger RNAbiologyUnfertilized EggsRNACell PolarityMembrane ProteinsCell Biologybiology.organism_classificationBlotting NorthernMolecular biologychemistrySea Urchinsembryonic structuresCortexColchicineFEBS Letters
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Latency versus persistence or intermittent recurrences: Evidence for a latent state of murine cytomegalovirus in the lungs

1997

The state of cytomegalovirus (CMV) after the resolution of acute infection is an unsolved problem in CMV research. While the term "latency" is in general use to indicate the maintenance of the viral genome, a formal exclusion of low-level persistent productive infection depends on the sensitivity of the assay for detecting infectious virus. We have improved the method for detecting infectivity by combining centrifugal infection of permissive indicator cells in culture, expansion to an infectious focus, and sensitive detection of immediate-early RNA in the infected cells by reverse transcriptase PCR. A limiting-dilution approach defined the sensitivity of this assay. Infectivity was thereby …

Lung DiseasesMuromegalovirusMolecular Sequence DataImmunologyCentrifugationGenome ViralViral Plaque AssayPolymerase Chain ReactionSensitivity and SpecificityMicrobiologylaw.inventionMiceMuromegalovirusRecurrencelawVirologyVirus latencymedicineAnimalsLatency (engineering)Cells CulturedPolymerase chain reactionVirus quantificationInfectivityMice Inbred BALB COrganizationsBase SequencebiologyRNAHerpesviridae Infectionsbiology.organism_classificationmedicine.diseaseVirologyVirus LatencyReverse transcription polymerase chain reactionInsect ScienceDNA ViralImmunologyFemaleResearch Article
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DIFFERENTIAL SCANNING CALORIMETRY STUDY ON DRUG RELEASE FROM AN INULIN-BASED HYDROGEL AND ITS INTERACTION WITH A BIOMEMBRANE MODEL:pH AND LOADING EFF…

2008

Inulin has been derivatized with methacrylic anhydride (MA) and succinic anhydride (SA) to obtain a methacrylated/succinilated derivative (INU-MA-SA) able to produce a pH sensitive hydrogel after UV irradiation. The hydrogel was characterized and loaded with diflunisal (10.4, 17 and 24%, w/w) chosen as a model drug. The drug release from INU-MA-SA-based hydrogel to a biomembrane model made by unilamellar vesicles of dimyristoylphosphatidyl-choline (DMPC) was investigated at pH 4.0 and 7.4 by differential scanning calorimetry (DSC) that appears to be a suitable technique to follow the transfer kinetics of a drug from a controlled release system to a biomembrane model. The drug release from t…

Magnetic Resonance SpectroscopyINULIN HYDROGELS DRUG RELEASE DIFFERENTIAL SCANNING CALORIMETRYPharmaceutical ScienceDiflunisalMethacrylic anhydrideCentrifugationInsulysinDosage formchemistry.chemical_compoundDifferential scanning calorimetryX-Ray DiffractionSpectroscopy Fourier Transform InfraredmedicineHypoglycemic AgentsChromatography High Pressure LiquidChromatographyCalorimetry Differential ScanningVesicleAnti-Inflammatory Agents Non-Steroidaltechnology industry and agricultureSuccinic anhydrideInulinHydrogelsMembranes ArtificialSuccinatesHydrogen-Ion ConcentrationDiflunisalControlled releaseMolecular WeightchemistryChemical engineeringSolubilitySelf-healing hydrogelsSpectrophotometry UltravioletChromatography Thin LayerDimyristoylphosphatidylcholinemedicine.drug
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Comparison of speed-vacuum method and heat-drying method to measure brain water content of small brain samples

2016

Abstract Background A reliable measurement of brain water content (wet-to-dry ratio) is an important prerequisite for conducting research on mechanisms of brain edema formation. The conventionally used oven-drying method suffers from several limitations, especially in small samples. A technically demanding and time-consuming alternative is freeze-drying. New method Centrifugal vacuum concentrators (e.g. SpeedVac/speed-vacuum drying) are a combination of vacuum-drying and centrifugation, used to reduce the boiling temperature. These concentrators have the key advantages of improving the freeze-drying speed and maintaining the integrity of dried samples, thus, allowing e.g. DNA analyses. In t…

Male0301 basic medicineHot TemperatureTime FactorsGenotyping TechniquesVacuumNeuroscience(all)Analytical chemistrySmall brainBrain EdemaCentrifugationBrain water03 medical and health sciences0302 clinical medicineBrain Injuries TraumaticAnimalsDesiccationWater contentBrain ChemistryMoistureChemistryBrain edemaGeneral Neurosciencetechnology industry and agricultureArea under the curveWaterMice Inbred C57BLDisease Models AnimalBoiling pointNeuroprotective AgentsSodium Bicarbonate030104 developmental biologyROC CurveArea Under CurveContent (measure theory)Feasibility Studies030217 neurology & neurosurgeryBiomedical engineeringJournal of Neuroscience Methods
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Viability, attachment efficiency, and xenobiotic metabolizing enzyme activities are well maintained in EDTA isolated rat liver parenchymal cells afte…

1995

Rat liver parenchymal cells were isolated by EDTA perfusion and were subsequently purified by Percoll centrifugation. The freshly isolated liver cells had a mean viability of 95% as judged by trypan blue exclusion. Isolated liver parenchymal cells were then stored at 0°C for up to 1 wk in University of Wisconsin solution (UW). During this hypothermic preservation, the viability was only slightly reduced to 92% after 1 d and to 85% after 3 d at 0°C. Thereafter, the viability decreased rapidly. After cold storage for up to 3 d, it was possible to use the parenchymal liver cells either in short-term suspension or in cell culture. The attachment efficiency in cell culture was the same for fresh…

MaleAdenosineCell SurvivalAllopurinolOrgan Preservation SolutionsCold storageBiologyXenobioticsRats Sprague-Dawleychemistry.chemical_compoundCryoprotective AgentsRaffinoseCell AdhesionAnimalsInsulinViaspanCentrifugationCells CulturedEdetic AcidCryopreservationCell BiologyGeneral MedicineGlutathioneMolecular biologyIn vitroEnzymesRatsLiverBiochemistrychemistryCell cultureTrypan blueStem cellPercollDevelopmental BiologyIn Vitro Cellular & Developmental Biology - Animal
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A discoidal lipoprotein from the coelomic fluid of the polychaete Nereis virens.

2005

A discoidal lipoprotein was isolated from the coelomic fluid of the polychaete, Nereis virens, by density gradient centrifugation. The lipoprotein was present in both sexes and moved as a uniform band in an agarose gel. The average diameter of the lipoprotein particles determined by electron microscopy was 42 nm with a thickness of 10 nm. SDS electrophoresis showed two apoprotein subunits with molecular masses of 247 and 85 kDa, respectively. In lectin blots, both apoproteins were reactive with Concanavalin A indicating the presence of N-glycans. The small subunit was also reactive with peanut lectin, indicating additional O-glycosylation. The total lipid content was 48% and consisted mainl…

MaleEmbryo NonmammalianGlycosylationPhysiologyLipoproteinsBiologyIn Vitro TechniquesBiochemistrychemistry.chemical_compoundPolysaccharidesAnimalsParticle SizeMolecular BiologyDifferential centrifugationMolecular massLectinPolychaetaLipidsThin-layer chromatographyBody FluidsMolecular WeightElectrophoresisProtein SubunitschemistryBiochemistryConcanavalin Abiology.proteinAgaroselipids (amino acids peptides and proteins)FemaleLipoproteinComparative biochemistry and physiology. Part B, Biochemistrymolecular biology
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