Search results for "Microscope"

showing 10 items of 1412 documents

Light field propagation by metal micro- and nanostructures

2001

The ability to sustain plasmon oscillations gives rise to unique properties of metal nanostructures, which can be exploited for the controlled manipulation of light fields on the nanoscale. In this context we investigate electromagnetic coupling effects within lithographically produced ensembles of gold nanoparticles with a photon scanning tunnelling microscope. To provide an interface between these nano-optical devices and classical far-field optics, we investigate surface plasmon propagation on microstructured metal thin films.

HistologyNanostructureMicroscopeMaterials sciencebusiness.industrySurface plasmonNanophotonicsPhysics::OpticsContext (language use)NanotechnologyPathology and Forensic Medicinelaw.inventionlawOptoelectronicsbusinessLight fieldPlasmonQuantum tunnellingJournal of Microscopy
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In vivo detection of cytokeratin filament network breakdown in cells treated with the phosphatase inhibitor okadaic acid.

2001

We have previously described vulva carcinoma-derived A-431 subclone AK13-1, which stably expresses fluorescently labeled cytokeratin filaments (CKFs). Time-lapse fluorescence microscopy of these cells permits the continuous monitoring of the dynamics of the CKF cytoskeleton in vivo. To study mechanisms and principles of CKF disassembly as it occurs, e.g., during mitosis and liver disease, we have treated cells with the phosphatase inhibitor okadaic acid (OA), which induces complete CKF network breakdown within 3–5 h without significantly affecting the organization of the actin- and tubulin-based cytofilaments. In time-lapse movies, we find that the network breakdown starts at the cell perip…

HistologyTime FactorsRecombinant Fusion ProteinsGreen Fluorescent ProteinsPathology and Forensic Medicinechemistry.chemical_compoundCytokeratinAdenosine TriphosphateStress FibersOkadaic AcidFluorescence microscopeTumor Cells CulturedHumansEnzyme InhibitorsPhosphorylationCytoskeletonMitosisActinCytoskeletonbiologyVulvar NeoplasmsEpithelial CellsCell BiologyOkadaic acidCell biologyCytoskeletal ProteinsLuminescent ProteinsTubulinchemistryDesmoplakinsMicroscopy FluorescenceCytoplasmbiology.proteinKeratinsFemaleIndicators and ReagentsCell and tissue research
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Imaging connected porosity of crystalline rock by contrast agent-aided X-ray microtomography and scanning electron microscopy

2017

We set out to study connected porosity of crystalline rock using X-ray microtomography and scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS) with caesium chloride as a contrast agent. Caesium is an important radionuclide regarding the final deposition of nuclear waste and also forms dense phases that can be readily distinguished by X-ray microtomography and SEM-EDS. Six samples from two sites, Olkiluoto (Finland) and Grimsel (Switzerland), where transport properties of crystalline rock are being studied in situ, were investigated using X-ray microtomography and SEM-EDS. The samples were imaged with X-ray microtomography, immersed in a saturated caesium chlorid…

HistologyX-ray microtomographyMaterials science010504 meteorology & atmospheric sciencesScanning electron microscopechemistry.chemical_elementMineralogyengineering.material010502 geochemistry & geophysics01 natural sciencesChloridePathology and Forensic Medicinechemistry.chemical_compoundSphaleritechemistryCaesiummedicineengineeringKaoliniteCaesium chloridePorosity0105 earth and related environmental sciencesmedicine.drugJournal of Microscopy
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Dual drug-loaded halloysite hybrid-based glycocluster for sustained release of hydrophobic molecules

2016

A dual drug-loaded HNT–CD glycocluster delivery system based on halloysite nanotubes and carbohydrate functionalized cyclodextrin was developed by a green protocol using solvent-free microwave irradiation. The nanohybrid was employed for concurrent load and release of silibinin and curcumin. The new delivery system was characterized by means of TGA, FT-IR spectroscopy, SEM and DLS. These techniques confirm the successful loading of the two drugs in the system. SEM and DLS measurements highlighted that the nanomaterial preserves a tubular structure with an average hydrodynamic radius of ca. 200 nm. The release of the drugs from the HNT glycocluster was investigated by means of UV-vis spectro…

Hydrodynamic radiusGeneral Chemical Engineering02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesHalloysiteNanomaterialsSettore MED/13 - EndocrinologiaFluorescence microscopeSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationbiologyCyclodextrinLectinGeneral ChemistrySettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesMembraneBiochemistrychemistryDrug deliveryengineeringbiology.proteinBiophysicshalloysite nanotubes glycocluster effect cyclodextrin curcumin and silibinin0210 nano-technology
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Osteogenesis imperfecta and hyperplastic callus formation: light- and electron-microscopic findings.

1993

In rare cases of osteogenesis imperfecta, an "overshoot" growth of new bone may occur, which, clinically gives the impression of a tumour. This condition is known as hyperplastic callus formation. Morphology showed an excessive mixed desmal-chondral osteoneogenesis. Atypical collagen fibrils in non-callus tissue represent an indicator for this callus formation in individual patients.

HyperplasiaCallus formationChemistryfungifood and beveragesAnatomyHyperplasiaOsteogenesis Imperfectamusculoskeletal systemmedicine.diseaseOsteochondrodysplasialaw.inventionbody regionsMicroscopy Electronsurgical procedures operativeOsteogenesis imperfectalawCallusmedicineHyperplastic callus formationHumansElectron microscopeBony CallusElectron microscopicGenetics (clinical)American journal of medical genetics
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Digital Image Processing in the Analysis of Astrometric Plates

1991

AbstractIn this paper, we display an improvement to our process of semi-automatic measuring of astrometric plates, in which the photometric sensor is substituted by a CCD system of image getting and digitalization. The advantages of this method are analyzed taking into account the possibilities of the image analysis in the space and frequency domain.

Image formationComputer sciencebusiness.industryBinary imageDigital imagingTop-hat transformImage processingDigital imageComputer graphics (images)Digital image processingComputer visionArtificial intelligencebusinessMicroscope image processingInternational Astronomical Union Colloquium
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Numerical simulations of photon scanning tunneling microscopy: role of a probe tip geometry in image formation

2005

Abstract Numerical simulations of two-dimensional probe–object system emulating a photon scanning tunnelling microscope are presented. R -matrix propagation algorithm incorporated into the differential method was used to achieve an extended capability to rigorously model a realistic system consisting of both a probe and a sample. Influence of the probe tip parameters on image formation in scanning near-field microscopy has been investigated. Coupling of the near-field to a single-mode probe and formation of a guided fundamental mode in a probe were investigated for various probe widths and lengths. The influence of the probe taper shape and apex size on near-field images was studied for sin…

Image formationScanning Hall probe microscopeMaterials scienceMicroscopebusiness.industryNear-field opticsAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic Materialslaw.inventionScanning probe microscopyOpticslawMicroscopyNear-field scanning optical microscopeElectrical and Electronic EngineeringPhysical and Theoretical ChemistryScanning tunneling microscopebusinessOptics Communications
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Analysis of image formation with a photon scanning tunneling microscope

1996

International audience; The photon scanning tunneling microscope (PSTM) is based on the frustration of a total internal reflected beam by the end of an optical fiber. Until now it has been used to obtain topographic information, generally for smooth samples. We report theoretical as well as experimental results on the observation of a step on a quartz substrate with the PSTM. These results demonstrate the effects on image formation of the distance between the fiber tip and the sample surface, the orientation of the incident beam with respect to the step, the polarization, and the coherence of the light. Good agreement exists between numerical simulations and experiments. We show that a pert…

Image formation[PHYS.PHYS.PHYS-OPTICS] Physics [physics]/Physics [physics]/Optics [physics.optics]Optical fiberScanning tunneling spectroscopy02 engineering and technology01 natural scienceslaw.invention010309 opticsScanning probe microscopyOpticslaw0103 physical sciencesLight beamPhysicsTotal internal reflection[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics][ PHYS.PHYS.PHYS-OPTICS ] Physics [physics]/Physics [physics]/Optics [physics.optics]business.industryNear-field optics021001 nanoscience & nanotechnologyAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsComputer Vision and Pattern RecognitionScanning tunneling microscopebusiness0210 nano-technology
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Human macrophages simultaneously express membrane-C1q and Fc-receptors for IgG

2005

Membrane C1q (mC1q) of macrophages (MPhi) is a precursor of the IgG-binding serum protein C1q. Thus, mC1q potentially provides one of several Fcgamma binding sites of mature MPhi and we analyzed whether simultaneous expression occurs of established receptors for IgG, FcgammaRI, II, and III, and mC1q during in vitro differentiation of MPhi. Using flow cytometry, immunoprecipitation combined with Western blotting and Northern blot analysis mC1q was hardly detected in freshly isolated blood monocytes, but increasingly in developing monocyte-derived MPhi. Laser scanning fluorescence microscopy confirmed the membrane localization of mC1q. Two-color-staining flow cytometry experiments indicated t…

ImmunoprecipitationCD14ImmunologyReceptors FcBiologyFlow cytometrymedicineFluorescence microscopeHumansImmunoprecipitationImmunology and AllergyNorthern blotReceptorCells Culturedmedicine.diagnostic_testComplement C1qMacrophagesCell MembraneCell DifferentiationMolecular biologyIn vitroCell biologyBlotGene Expression RegulationImmunoglobulin GProtein BindingImmunology Letters
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A Protein-Interaction Array Inside a Living Cell

2013

Cell phenotype is determined by protein network states that are maintained by the dynamics of multiple protein interactions.1 Fluorescence microscopy approaches that measure protein interactions in individual cells, such as by Forster resonant energy transfer (FRET), are limited by the spectral separation of fluorophores and thus are most suitable to analyze a single protein interaction in a given cell. However, analysis of correlations between multiple protein interactions is required to uncover the interdependence of protein reactions in dynamic signal networks. Available protein-array technologies enable the parallel analysis of interacting proteins from cell extracts, however, they can …

ImmunoprecipitationRecombinant Fusion Proteinsprotein-protein interactionsImmobilized Nucleic AcidsProtein Array AnalysisreceptorsDNA Single-StrandedCatalysisProtein–protein interactionReceptors G-Protein-CoupledBimolecular fluorescence complementationProtein Array AnalysisChlorocebus aethiopsFluorescence microscopeFluorescence Resonance Energy TransferAnimalsProtein Interaction MapsProtein kinase Amultiplexed assayChemistryProteinsProtein-protein interactions Dip Pen Nanolithography Protein KinaseDNA directed immobilizationGeneral MedicineGeneral ChemistryCommunicationssurface-immobilizationKineticsLuminescent ProteinsFörster resonance energy transferBiochemistryMicroscopy FluorescenceCOS CellsBiophysicsSignal transductionAntibodies Immobilizedsignal transduction
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