Search results for "Staining and Labeling"

showing 10 items of 150 documents

Ultrastructural changes of the oenocytes of Gryllus bimaculatus DEG (Saltatoria, Insecta) during the moulting cycle

1974

1. The oenocytes of Gryllus bimaculatus are characterized by an abundant smooth-surfaced ER (ATER). In spite of the great cell size the plasma membrane never shows extensive infoldings during the moulting cycle. In addition to mitochondria there are very large numbers of microbodies containing peroxidase but apparently not uricase. Within the second part of the instar the microbodies lie along the clefts which run through the whole cell. 2. The following changes are observed in the course of a moulting cycle: Immediately after hatching the ATER is scarcely developed, some liposomes are located within areas of ATER disappearing some hours later. 20 hours after emergence glycogen deposits app…

EcdysoneInsectaTime FactorsHistologyGolgi ApparatusMicrobodiesPathology and Forensic Medicinechemistry.chemical_compoundAnimalsMicrobodyOvumCell NucleusStaining and LabelingGlycogenbiologyHistocytochemistryHatchingGryllus bimaculatusCell MembraneMetamorphosis BiologicalCell BiologyAnatomybiology.organism_classificationMitochondriaCell biologyMicroscopy ElectronchemistryLarvaUltrastructureInstarFemaleLysosomesMoultingReticulumGlycogenCell and Tissue Research
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Sea urchin embryos as a model system for studying autophagy induced by cadmium stress

2011

It is well known that sea urchin embryos are able to activate different defense strategies against stress. We previously demonstrated that cadmium treatment triggers the accumulation of metal in embryonic cells and the activation of defense systems depending on concentration and exposure time, through the synthesis of heat shock proteins and/or the initiation of apoptosis. Here we show that Paracentrotus lividus embryos exposed to Cd adopt autophagy as an additional stratagem to safeguard the developmental program. At present, there are no data focusing on the role of this process in embryo development of marine organisms. In this paper we utilized different techniques to detect autophagy i…

Embryo Nonmammaliananimal structuresImmunoblottingFluorescent Antibody Techniquechemistry.chemical_elementBiologyModels BiologicalParacentrotus lividusStress PhysiologicalHeat shock proteinBotanyAutophagyAnimalsSettore BIO/06 - Anatomia Comparata E Citologiaautophagy cadmium stress acidic vesicular organelles bafilomycin A1 LC3 Paracentrotus lividus embryosMolecular BiologyOrganellesCadmiumStaining and LabelingAutophagyEmbryogenesisEmbryoCell Biologybiology.organism_classificationEmbryonic stem cellAcridine OrangeCell biologychemistryNeutral RedApoptosisembryonic structuresParacentrotusMicrotubule-Associated ProteinsCadmiumDensitometryAutophagy
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Phasor-FLIM analysis of Thioflavin T self-quenching in Concanavalin amyloid fibrils

2020

The formation of amyloid structures has traditionally been related to human neurodegenerative pathologies and, in recent years, the interest in these highly stable nanostructures was extended to biomaterial sciences. A common method to monitor amyloid growth is the analysis of Thioflavin T fluorescence. The use of this highly selective dye, diffused worldwide, allows mechanistic studies of supramolecular assemblies also giving back important insight on the structure of these aggregates. Here we present experimental evidence of self-quenching effect of Thioflavin T in presence of amyloid fibrils. A significant reduction of fluorescence lifetime of this dye which is not related to the propert…

Fluorescence-lifetime imaging microscopyAmyloidFLIMHistologyAmyloid02 engineering and technologyProtein aggregationprotein aggregation03 medical and health scienceschemistry.chemical_compound0302 clinical medicineself-quenchingmental disordersamyloid fibrilConcanavalin Afluorescence lifetimeHumansBenzothiazolesInstrumentationFluorescent DyesInclusion BodiesQuenching (fluorescence)biologyStaining and LabelingChemistryOptical ImagingPhasorNeurodegenerative Diseases030206 dentistry021001 nanoscience & nanotechnologyFluorescenceSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Medical Laboratory TechnologyMicroscopy FluorescenceConcanavalin APhasorbiology.proteinBiophysicsThioflavin TThioflavinamyloid fibrils Concanavalin A FLIM fluorescence lifetime Phasor protein aggregation self-quenching Thioflavin TAnatomy0210 nano-technology
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Site-specific near-infrared fluorescent labelling of proteins on cysteine residues with meso -chloro-substituted heptamethine cyanine dyes

2018

International audience; Near-infrared (NIR) fluorescence imaging is a promising new medical imaging modality. Associated with a targeting molecule, NIR fluorophores can accumulate selectively in tissues of interest and become valuable tools for the diagnosis and therapy of various pathologies. To facilitate the design of targeted NIR imaging agents, it is important to identify simple and affordable fluorescent probes, allowing rapid labelling of biovectors such as proteins, ideally in a site-specific manner. Here, we demonstrate that heptamethine cyanine based fluorophores, such as IR-783, that contain a chloro-cyclohexyl moiety within their polymethine chain can react selectively, at neutr…

Fluorescence-lifetime imaging microscopyFluorophoreHalogenationProteins on cysteine residuesInfrared Rays010402 general chemistry01 natural sciencesBiochemistrychemistry.chemical_compoundMiceLabellingCell Line TumorMoietyAnimalsTissue Distribution[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyAmino Acid SequenceCysteinePhysical and Theoretical ChemistryCyanineheptamethine cyanine dyesPeptide sequenceFluorescent DyesStaining and Labeling010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistryOptical ImagingProteinsCarbocyaninesFluorescenceCombinatorial chemistry0104 chemical sciences3. Good healthPeptidesCysteine
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18F-Labeling Using Click Cycloadditions

2014

Due to expanding applications of positron emission tomography (PET) there is a demand for developing new techniques to introduce fluorine-18 (t1/2=109.8 min). Considering that most novel PET tracers are sensitive biomolecules and that direct introduction of fluorine-18 often needs harsh conditions, the insertion of18F in those molecules poses an exceeding challenge. Two major challenges during18F-labeling are a regioselective introduction and a fast and high yielding way under mild conditions. Furthermore, attention has to be paid to functionalities, which are usually present in complex structures of the target molecule. The Cu-catalyzed azide-alkyne cycloaddition (CuAAC) and several copper…

Fluorine RadioisotopesGeneral Immunology and MicrobiologyCycloaddition ReactionStaining and LabelingComputer sciencelcsh:Rlcsh:MedicineNanotechnologyGeneral MedicineReview ArticleHigh yieldingGeneral Biochemistry Genetics and Molecular BiologyCycloadditionCatalysis18f labelingClick chemistryAnimalsClick ChemistryPet tracerCopperBioMed Research International
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Membrane potential dye imaging of ventromedial hypothalamus neurons from adult mice to study glucose sensing

2013

Studies of neuronal activity are often performed using neurons from rodents less than 2 months of age due to the technical difficulties associated with increasing connective tissue and decreased neuronal viability that occur with age. Here, we describe a methodology for the dissociation of healthy hypothalamic neurons from adult-aged mice. The ability to study neurons from adult-aged mice allows the use of disease models that manifest at a later age and might be more developmentally accurate for certain studies. Fluorescence imaging of dissociated neurons can be used to study the activity of a population of neurons, as opposed to using electrophysiology to study a single neuron. This is par…

General Chemical Engineeringneurons/cytology/metabolism/ physiologystaining and labeling/ methodsventromedial hypothalamic[ SDV.BA ] Life Sciences [q-bio]/Animal biologyMembrane Potentials0302 clinical medicinePremovement neuronal activity[SDV.BDD]Life Sciences [q-bio]/Development BiologyNeuronsMembrane potential0303 health scienceseducation.field_of_studyGeneral Neuroscience[SDV.BA]Life Sciences [q-bio]/Animal biologynucleus/cytology/metabolism/ physiologyanimalsmedicine.anatomical_structureHypothalamus[SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]fluorescent dyes/ chemistryinbred c57blmicePopulationConnective tissuefluorescence/ methodsBiologyGeneral Biochemistry Genetics and Molecular Biologyspectrometry03 medical and health sciencesmaleExtracellularmedicine[ SDV.BDD ] Life Sciences [q-bio]/Development BiologyeducationFluorescent Dyes030304 developmental biologyStaining and LabelingGeneral Immunology and Microbiologymembrane potentials/physiologyMice Inbred C57BLElectrophysiologyGlucoseSpectrometry Fluorescencenervous systemVentromedial Hypothalamic Nucleus[ SDV.NEU ] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]NeuronNeuroscience030217 neurology & neurosurgeryglucose/ metabolismNeuroscience
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Demonstration of endogenous lectins in synovial tissue.

1991

We have recently shown that synoviocytes and extracellular matrices exhibit distinct patterns of carbohydrate expression. Their biological relevance is however not known. The purpose of the present study was to find out whether human synovial tissue would also show a specific receptor pattern for complex sugar molecules. Endogenous lectins were displayed by means of biotinylated neoglycoproteins and sulfated polysaccharides in paraffin-embedded material or cryosections. In addition to certain carbohydrate components that are known to be constituents of the carbohydrate part of cellular glycoconjugates, our panel included heparin and fucoidan, a sulfated fucose. Binding sites were shown usin…

GlycoconjugateBiopsyImmunologyReceptors Cell SurfaceBiologyFucoseArthritis Rheumatoidchemistry.chemical_compoundRheumatologyReference ValuesSynovitisLectinsOsteoarthritismedicineImmunology and AllergyHumansReceptorchemistry.chemical_classificationStaining and LabelingHistocytochemistrySynovial MembraneLectinAntibodies MonoclonalGeneral Medicinemedicine.diseasemedicine.anatomical_structureBiochemistrychemistrySynovial CellBiotinylationImmunologybiology.proteinCarbohydrate MetabolismSynovial membraneScandinavian journal of rheumatology
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Unusual basement layer in the midgut of gammaridean Niphargus virei Chevreux (Crustacea, Amphipoda).

1988

The basement membrane of the midgut and posterior caeca epithelium in the gammaridean amphipod Niphargus virei Chevreux, 1896 is made of an unusual structure. This basal lamina, properly called “basal layer”, shows a dense sheet formed by a system of dense hexagonal plates connected by thin filaments. Histochemical studies and enzymatic reactions lead to the conclusion that these structures are proteinaceous, without collagenous protein, and embedded in a neutral polysaccharide matrix. The possible mechanical significance of these mesenteric structures is discussed.

HistologyAmphipodaMatrix (biology)Basement MembraneCrustaceamedicineAnimalsMolecular BiologyBasement membranebiologyStaining and LabelingHistocytochemistryProteinsMidgutCell BiologyGeneral MedicineAnatomybiology.organism_classificationCrustaceanEpitheliumMedical Laboratory TechnologyMicroscopy Electronmedicine.anatomical_structureBasal laminaCollagenAnatomyGeneral Agricultural and Biological SciencesLayer (electronics)Digestive SystemHistochemistry
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Supravital Uptake of Methylene Blue by Dendritic Cells within Stratified Squamous Epithelia: a Light and Electron Microscope Study

1996

Electron microscopic data on methylene blue staining of dendritic cells in the epithelia of the soft palate and skin of the mouse after supravital dye injection are presented. The ultra-structural details were compared with corresponding light microscopic findings. Methylene blue stained tissue was fixed by immersion in a paraformaldehyde-glutaraldehyde solution containing phosphomolybdic acid. The ensuing dye precipitate was stabilized by ammonium heptamolybdate. The light microscopic investigation revealed that selective staining of dendritic cells depended on the presence of ambient oxygen. In addition, delicate morphological characteristics, like spinous structures of the dendrites, wer…

HistologyConnective tissueEpitheliumlaw.inventionMicechemistry.chemical_compoundlawOrganellemedicineAnimalsColoring AgentsSkinParaffin EmbeddingStaining and LabelingEpithelial CellsDendritic CellsGeneral MedicineEpitheliumStainingMethylene BlueMicroscopy ElectronMedical Laboratory Technologymedicine.anatomical_structureVital stainchemistryBiochemistryCytoplasmBiophysicsPalate SoftElectron microscopeMethylene blueBiotechnic & Histochemistry
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Differential staining of mucin granules from epoxy resin sections by a phosphotungstic acid-methyl green procedure.

1991

After treatment of epoxy resin semithin sections from glutaraldehyde fixed rat large intestine with 5% aqueous phosphotungstic acid (PTA), staining with unpurified 0.2% solutions of methyl green at 60 C for 5 min produces a color differentiation between mucin granules of goblet cells. Some mucin granules and the glycocalyx appear deep green while the remaining granules, luminal mucin and collagen fibers are pink. The known contamination of unpurified methyl green with crystal violet seems to be responsible for the pink staining reaction of the latter structures, which also present an orange-red fluorescence under green exciting light. Electron microscopic observations show selective contras…

HistologyCytoplasmic Granuleslaw.inventionGlycocalyxchemistry.chemical_compoundMethyl GreenlawAnimalsPhosphotungstic acidCrystal violetIntestine LargeStaining and LabelingDifferential stainingEpoxy ResinsGastric MucinsMucinRats Inbred StrainsGeneral MedicinePhosphotungstic AcidStainingRatsMedical Laboratory TechnologyMicroscopy ElectronchemistryBiochemistryGentian VioletGlutaraldehydeElectron microscopeNuclear chemistryBiotechnichistochemistry : official publication of the Biological Stain Commission
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