Search results for "Confocal microscopy"

showing 10 items of 120 documents

Confocal microscopy study of the distribution, content and activity of mitochondria during Paracentrotus lividus development

2007

Summary In the present paper we applied confocal microscopy andfluorescence technologies for studying the distribution andthe oxidative activity of sea urchin ( Paracentrotus lividus )mitochondria during development, by in vivo incubating eggsand embryos with cell-permeant MitoTracker probes. Wecalculated, by a mathematical model, the intensity values, the variations of intensity, and the variation index of incorporatedfluorochromes. Data demonstrate that mitochondrial massdoes not change during development, whereas mitochondrialrespirationincreases.Inaddition,startingfrom16blastomeresstage, some regions of the embryo contain organelles moreactive in oxygen consumption. Introduction The con…

Embryo NonmammalianHistologyConfocal laser scanning microscopeNanotechnologyMitochondrionParacentrotus lividussea urchinPathology and Forensic Medicinelaw.inventionIn vivoConfocal microscopylawdevelopment; sea urchin; mitochondrial mass; CLSMbiology.animalOrganelleMicroscopyAnimalsdevelopmentSea urchinmitochondrial maMicroscopy Confocalbiologybiology.organism_classificationMitochondriaOxygenParacentrotusBiophysicsCLSMOxidation-ReductionJournal of Microscopy
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Effects of acids used in the microabrasion technique: microhardness and confocal microscopy analysis

2015

Background: This study evaluated the effects of the acids used in the microabrasion on enamel. Material and Methods: Seventy enamel/dentine blocks (25 mm 2 ) of bovine incisors were divided into 7 groups (n=10). Experimental groups were treated by active/passive application of 35% H 3 PO 4 (E1/E2) or 6.6% HCl (E3/ E4). Control groups were treated by microabrasion with H 3 PO 4 +pumice (C5), HCl+silica (C6), or no treatment (C7). The superficial (SMH) and cross-sectional (CSMH; depths of 10, 25, 50, and 75 μm) microhardness of enamel were analyzed. Morphology was evaluated by confocal laser-scanning microscopy (CLSM). Data were analyzed by analysis of variance (Proc Mixed), Tukey, and Dunnet…

Enamel paintChemistryConfocalResearchMineralogyOdontologíaEsthetic Dentistry:CIENCIAS MÉDICAS [UNESCO]Indentation hardnessCiencias de la saludlaw.inventionstomatognathic systemConfocal microscopylawvisual_artUNESCO::CIENCIAS MÉDICASvisual_art.visual_art_mediumGeneral DentistryNuclear chemistry
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PLLA/Fibrin Tubular Scaffold: A New Way for Reliable Endothelial Cell Seeding

2014

In the present work a simple and quick technique for cell seeding into tubular-shaped scaffolds, which allows a homogeneous cell distribution, was tested. The poly-L-lactide (PLLA) scaffolds, prepared via diffusion induced phase separation (DIPS), were filled with fibrin gel in order to obtain a hybrid scaffold for Vascular Tissue Engineering applications. The formation of immobilized fibrin networks on the inner surface of the tubular scaffolds was observed using confocal microscopy and SEM. Morphological analysis of the so-obtained scaffold revealed that the fibrin gel is uniformly distributed on the internal surface of the scaffold, leading to an organized structure. Moreover a penetrati…

FibrinScaffoldMaterials sciencebiologyCell growthGeneral MedicinePenetration (firestop)Fibrinlaw.inventionEndothelial stem cellPhase SeparationTubular scaffoldConfocal microscopylawbiology.proteinSeedingVascular Tissue EngineeringBiomedical engineeringConference Papers in Science
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Protein diffusion in mammalian cell cytoplasm.

2011

We introduce a new method for mesoscopic modeling of protein diffusion in an entire cell. This method is based on the construction of a three-dimensional digital model cell from confocal microscopy data. The model cell is segmented into the cytoplasm, nucleus, plasma membrane, and nuclear envelope, in which environment protein motion is modeled by fully numerical mesoscopic methods. Finer cellular structures that cannot be resolved with the imaging technique, which significantly affect protein motion, are accounted for in this method by assigning an effective, position-dependent porosity to the cell. This porosity can also be determined by confocal microscopy using the equilibrium distribut…

Fluorescence-lifetime imaging microscopyCytoplasmMass diffusivity01 natural sciencesBiophysics Simulationslaw.inventionDiffusionlawMolecular Cell BiologyImage Processing Computer-Assistedprotein diffusionMammals0303 health sciencesMultidisciplinaryMicroscopy ConfocalChemistrysolulimaPhysicsQRCell biologyMedicineproteiinin diffuusioPorosityFluorescence Recovery After PhotobleachingResearch ArticleScienceCellsBiophysicsFluorescence correlation spectroscopyModels Biological03 medical and health sciencesdiffuusio (fysikaaliset ilmiöt)Bacterial ProteinsConfocal microscopy0103 physical sciencesAnimalsHumansComputer Simulation010306 general physicsBiology030304 developmental biologyNucleoplasmProtein transportta114ta1182Fluorescence recovery after photobleachingProteinsReproducibility of ResultssoluPhotobleachingProteiinien kuljetusLuminescent ProteinsMicroscopy FluorescenceCytoplasmCatsCellHeLa CellsPloS one
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Optical sectioning by two-pinhole confocal fluorescence microscopy.

2003

A two-pinhole axially superresolving confocal fluorescence imaging system is presented. Based on the concept of subtractive incoherent imaging, the system described here is equipped with a zero-focus complex-transmittance pupil filter in one of the collector paths. The optical sectioning capacity of the system is 25% superior to that of a free-pupil one-pinhole instrument.

Fluorescence-lifetime imaging microscopyMaterials scienceMicroscopy ConfocalOptical sectioningbusiness.industryConfocalScanning confocal electron microscopyGeneral Physics and AstronomyCell BiologyModels TheoreticalImage Enhancementlaw.inventionOpticsMicroscopy FluorescenceStructural BiologyConfocal microscopylawLight sheet fluorescence microscopySubtraction TechniqueMicroscopyGeneral Materials SciencePinhole (optics)businessMicron (Oxford, England : 1993)
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Polish is quantitatively different on quartzite flakes used on different worked materials.

2020

Metrology has been successfully used in the last decade to quantify use-wear on stone tools. Such techniques have been mostly applied to fine-grained rocks (chert), while studies on coarse-grained raw materials have been relatively infrequent. In this study, confocal microscopy was employed to investigate polished surfaces on a coarse-grained lithology, quartzite. Wear originating from contact with five different worked materials were classified in a data-driven approach using machine learning. Two different classifiers, a decision tree and a support-vector machine, were used to assign the different textures to a worked material based on a selected number of parameters (Mean density of furr…

Future studiesConfocal MicroscopyDecision AnalysisLithologyRaw MaterialsAntlersBone imagingPlant Science01 natural sciencesDiagnostic RadiologyMedicine and Health Sciences0601 history and archaeologyElectron MicroscopyAnimal AnatomyMaterialsMicroscopyMultidisciplinary060102 archaeologyPlant AnatomyRadiology and ImagingQRLight Microscopy06 humanities and the artsQuartzWoodBone ImagingProcess EngineeringPhysical SciencesMedicineEngineering and TechnologyScanning Electron MicroscopyAnatomyManagement EngineeringGeologyResearch Article010506 paleontologyImaging TechniquesScienceMaterials ScienceMineralogyIndustrial ProcessesResearch and Analysis MethodsDiagnostic MedicineIndustrial Engineering0105 earth and related environmental sciencesSurface TreatmentsDecision TreesBiology and Life SciencesManufacturing ProcessesSample size determinationZoologyPloS one
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Synthesis of polymer materials for use as cell culture substrates

2007

International audience; Up to today, several techniques have been used to maintain cells in culture for studying many aspects of cell biology and physiology. More often, cell culture is dependent on proper anchorage of cells to the growth surface. Thus, poly-L-lysine, fibronectin or laminin are the most commonly used substrates. In this study, electrosynthesized biocompatible polymer films are proposed as an alternative to these standard substrates. The electrosynthesized polymers tested were polyethylenimine, polypropylenimme and polypyrrole. Then, the adhesion, proliferation and morphology of rat neuronal cell lines were investigated on these polymer substrates in an attempt to develop ne…

General Chemical EngineeringCellular differentiationNanotechnology02 engineering and technologyCell morphologylaw.invention03 medical and health scienceschemistry.chemical_compoundConfocal microscopylaw[CHIM]Chemical Sciencespolymers030304 developmental biology0303 health sciencesPolyethyleniminecell culture[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]atomic force microscopybiologyCell growthneurosciencesmicrosystemAdhesion021001 nanoscience & nanotechnologyFibronectinchemistryelectrochemistryCell culturebiology.proteinBiophysics0210 nano-technology
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Development of a green fluorescent tagged strain of Aspergillus carbonarius to monitor fungal colonization in grapes.

2011

An enhanced green fluorescent protein has been used to tag an OTA-producing strain of Aspergillus carbonarius (W04-40) isolated from naturally infected grape berries. Transformation of the fungus was mediated by Agrobacterium tumefaciens. The most efficient transformation occurred when the co-cultivation was done with 104 conidia due to higher frequency of resistance colonies (894 per 104 conidia) and lower background obtained. To confirm the presence of the hph gene in hygromycin resistant colonies, 20 putative transformants were screened by PCR analysis. The hph gene was identified in all the transformants. Variation on the expression levels of the eGFP was detected among the transformant…

GrapesOchratoxin productionHyphaGreen Fluorescent ProteinsHyphaeWineFood ContaminationAspergillus carbonariusMicrobiologyGreen fluorescent proteinMicrobiologyConidiumTransformation GeneticATMTGreen fluorescent proteinVitisDNA FungalAspergillusMicroscopy ConfocalbiologyStrain (chemistry)fungiFungal geneticsGene Transfer TechniquesGeneral MedicineAgrobacterium tumefaciensSpores Fungalbiology.organism_classificationOchratoxinsConfocal microscopyTransformation (genetics)Phosphotransferases (Alcohol Group Acceptor)AspergillusAgrobacterium tumefaciensCinnamatesConsumer Product SafetyFruitHygromycin BFood SciencePlasmidsInternational journal of food microbiology
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Effects of caspase inhibitors (z-VAD-fmk, z-VDVAD-fmk) on Nile Red fluorescence pattern in 7-ketocholesterol-treated cells: Investigation by flow cyt…

2007

Background: The 7-ketocholesterol (7KC)-induced cell death has some characteristics of apoptosis and is associated with polar lipid accumulation. So, we investigated the effects of the broad-spectrum caspase inhibitor z-VAD-fmk and of the caspase-2 inhibitor z-VDVAD-fmk on lipid profile evaluated by staining with Nile Red (NR). Methods: The 7KC-treated human monocytic U937 cells were cultured in the absence or in the presence of the caspase inhibitors z-VAD-fmk or z-VDVAD-fmk. When staining with NR is performed, neutral and polar lipids have yellow and orange/red emission, respectively, and fluorescence was then analyzed by flow cytometry (FCM) and by confocal laser scanning microscopy (CLS…

HistologyConfocalCaspase 2FluorescencePathology and Forensic Medicinelaw.inventionFlow cytometryAmino Acid Chloromethyl Ketones03 medical and health scienceschemistry.chemical_compound0302 clinical medicineConfocal microscopylawOxazinesmedicineImage Processing Computer-AssistedHumans[ SDV.IB ] Life Sciences [q-bio]/BioengineeringEnzyme InhibitorsKetocholesterols030304 developmental biology[SDV.IB] Life Sciences [q-bio]/BioengineeringCell Nucleus0303 health sciencesMicroscopyMicroscopy Confocalbiologymedicine.diagnostic_testNile redLipid metabolismCell BiologyU937 CellsFlow CytometryLipid MetabolismFluorescenceMolecular biologyCaspase Inhibitors3. Good healthStainingchemistry030220 oncology & carcinogenesisbiology.protein[SDV.IB]Life Sciences [q-bio]/Bioengineeringbiological phenomena cell phenomena and immunityFactor Analysis Statistical
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Depth profiles of aggregate centers and nanodefects in LiF crystals irradiated with 34 MeV 84Kr, 56 MeV 40Ar and 12 MeV 12C ions

2018

I. Manika, J. Maniks and R. Zabels acknowledge the national project IMIS2. A. Dauletbekova, A. Akilbekov, M. Zdorovets and A. Seitbayev acknowledge the GF AP05134257of Ministry of Education and Science the Republic of Kazakhstan.

IONSMaterials sciencePhotoluminescenceF2 AND F3^+ CENTERSDislocationsAGGREGATESFLUORINE COMPOUNDS02 engineering and technologyETCHING7. Clean energy01 natural sciencesFluenceENERGY DISSIPATIONIonIRRADIATION EXPERIMENTSLIF CRYSTALION BOMBARDMENT0103 physical sciencesF2 and F3 + centersMaterials Chemistry:NATURAL SCIENCES:Physics [Research Subject Categories]IrradiationLUMINESCENCE INTENSITYPhotoluminescenceLITHIUM COMPOUNDS010302 applied physicsLiF crystalsNANOHARDNESSDISLOCATIONS (CRYSTALS)Surfaces and InterfacesGeneral ChemistryNanoindentation021001 nanoscience & nanotechnologyCondensed Matter PhysicsIsotropic etchingSurfaces Coatings and FilmsLASER SCANNING CONFOCAL MICROSCOPYNANOINDENTATION TECHNIQUESIon irradiationCOLOR CENTERSHardeningELECTRONIC ENERGY LOSSAtomic physicsDislocationLUMINESCENCE SIGNALS0210 nano-technologyLuminescenceDamage depth profiles
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