Search results for "Staining"

showing 10 items of 449 documents

Instant labeling of therapeutic cells for multimodality imaging

2020

Autologous therapeutic cells are typically harvested and transplanted in one single surgery. This makes it impossible to label them with imaging biomarkers through classical transfection techniques in a laboratory. To solve this problem, we developed a novel microfluidic device, which provides highly efficient labeling of therapeutic cells with imaging biomarkers through mechanoporation. Methods: Studies were performed with a new, custom-designed microfluidic device, which contains ridges, which compress adipose tissue-derived stem cells (ADSCs) during their device passage. Cell relaxation after compression leads to cell volume exchange for convective transfer of nanoparticles and nanoparti…

SwineCellMedicine (miscellaneous)Multimodal Imaging030218 nuclear medicine & medical imagingin vivo cell tracking03 medical and health scienceschemistry.chemical_compound0302 clinical medicineIn vivoFluorodeoxyglucose F18medicinemicrofluidic deviceAnimalsMagnetite NanoparticlesPharmacology Toxicology and Pharmaceutics (miscellaneous)mechanoporationCells Culturedmedicine.diagnostic_testStaining and LabelingChemistryStem Cellsiron oxide nanoparticlesMagnetic resonance imagingTransfectionMagnetic Resonance Imaging18F-FDGmedicine.anatomical_structureAdipose TissuePositron emission tomography030220 oncology & carcinogenesisPositron-Emission TomographyStem cellIron oxide nanoparticlesEx vivoBiomarkersBiomedical engineeringResearch PaperTheranostics
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Increased acidophilia of eosinophil granules after EDTA treatment

1986

The acidophilic reaction of eosinophil leucocyte granules from human, pig and horse blood smears was investigated by using May-Grünwald-Giemsa staining after previous treatment with EDTA and sodium citrate solutions. The same peak at 530 nm, but absorption values considerably higher than those of controls, were found in eosinophil granules after application of chelating agents, indicating that removal of metal cations could unmask basic groups in these structures.

SwineEdta treatmentBiologyCytoplasmic GranulesAzure Stainschemistry.chemical_compoundPhenothiazinesHorse bloodSodium citratemedicineAnimalsHumansChelationHorsesEdetic AcidGranule (cell biology)Cell BiologyHydrogen-Ion ConcentrationEosinophilStainingEosinophilsmedicine.anatomical_structureBiochemistrychemistryCytophotometryAnatomyEosinophil leucocyteThe Histochemical Journal
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The Innervation of Taste Buds in the Soft Palate and Circumvallate Papilla of the Rat as Revealed by the Zinc Iodide-Osmium Tetroxide Technique.

1998

The taste buds in the soft palate and the circumvallate papillae of the rat were investigated by the zinc iodide-osmium tetroxide technique. In addition, electron micrographs of taste buds stained with this method were presented for the first time. Differences in taste bud structures were found between the examined regions. The taste buds of the soft palate showed a complicated plexus of intragemmal nerve fibers. Some fibers exhibited terminal polymorphic swellings. Single branches could be traced close to the space of the taste pore. In the soft palate, the taste bud cells remained unstained, whereas in the circumvallate papillae of the tongue, a subpopulation of taste bud cells could be s…

TasteHistologyOsmium TetroxideRats Sprague-DawleyFixativeschemistry.chemical_compoundNerve FibersTongueTongueTaste budmedicineAnimalsColoring AgentsLingual papillaSoft palateAnatomyIodidesTaste BudsAxonsRatsCell biologyStainingmedicine.anatomical_structureOsmium tetroxidechemistryZinc CompoundsCytoplasmPalate SoftArchives of Histology and Cytology
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Cytotoxicity and bioactivity of various pulpotomy materials on stem cells from human exfoliated primary teeth.

2017

Aims To investigate the cytotoxicity and bioactivity of several pulpotomy materials: Biodentine (Septodont, Saint-Maur-des-Fosses, France) MTA (Angelus, Londrina, PR, Brazil), Theracal LC (Bisco Inc., Schamburg, IL, USA) and IRM (Dentsply DeTrey GmbH, Konstanz, Germany), after contact with stem cells isolated from human exfoliated primary teeth (SHEDs). Methodology SHEDs were cultured in the presence of the eluates of various pulpotomy materials for 24, 48 and 72 h. Cell viability was determined by mitochondrial dehydrogenase enzymatic (MTT) assay. Apoptosis and changes in cell phenotype were evaluated by flow cytometry. Also, an in vitro scratch wound-healing assay was used to determine th…

Time FactorsCell SurvivalPulpotomyDentistryApoptosis02 engineering and technologyMatrix (biology)In Vitro TechniquesCell morphologyFlow cytometry03 medical and health sciences0302 clinical medicineCell MovementMaterials TestingmedicineHumansMethylmethacrylatesViability assayTooth DeciduousZinc Oxide-Eugenol CementCytotoxicityAluminum CompoundsGeneral DentistryCells Culturedmedicine.diagnostic_testChemistrybusiness.industrySilicatesStem CellsOxides030206 dentistryCalcium Compounds021001 nanoscience & nanotechnologyFlow CytometryMolecular biologyStainingDrug CombinationsPhenotypeApoptosisPulpotomyMicroscopy Electron Scanning0210 nano-technologybusinessPulp Capping and Pulpectomy AgentsInternational endodontic journal
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Electron Microscopic Contrast of the Cytoskeleton and Junctional Complexes of Intestinal Epithelial Cells by Ethanolic Phosphotungstic Acid

2000

After glutaraldehyde fixation and treatment with ethanolic phosphotungstic acid (E-PTA) before plastic embedding, sections of rat large intestine showed a characteristic electron contrasting pattern in epithelial cells. The axis of microvilli, terminal web, a thin band below the luminal plasma membrane, centrioles and junctional complexes (tight junctions, adherens junctions, and desmosomes) appeared highly contrasted. In addition to protein components of microfilaments and intermediate filaments, proteins from the junctional complexes could also be implicated in the contrasting reaction with E-PTA. Mitochondrial membranes, chromatin masses, and nucleoli of enterocytes showed considerable e…

Tissue FixationBiologyMicrofilamentSpecimen HandlingAdherens junctionTerminal webGlycocalyxchemistry.chemical_compoundAnimalsIntestine LargePhosphotungstic acidIntestinal MucosaRats WistarCytoskeletonIntermediate filamentCytoskeletonEthanolMicrovilliStaining and LabelingTissue EmbeddingTight junctionEpithelial CellsPhosphotungstic AcidAgricultural and Biological Sciences (miscellaneous)ChromatinMitochondriaRatsCell biologySolutionsMicroscopy ElectronIntercellular JunctionschemistrySolventsAnatomyCell NucleolusEuropean Journal of Morphology
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2021

The presence and interaction of immune cells in the tumor microenvironment is of significant importance and has a great impact on disease progression and response to therapy. Hence, their identification is of high interest for prognosis and treatment decisions. Besides detailed phenotypic analyses of immune, as well as tumor cells, spatial analyses is an important parameter in the complex interplay of neoplastic and immune cells—especially when moving into focus efforts to develop and validate new therapeutic strategies. Ex vivo analysis of tumor samples by immunohistochemistry staining methods conserves spatial information is restricted to single markers, while flow cytometry (disrupting t…

Tumor microenvironmentmedicine.diagnostic_testMelanomaOrganic ChemistryGeneral MedicineBiologymedicine.diseaseCatalysisComputer Science ApplicationsFlow cytometryStainingInorganic ChemistryImmune systemHumanized mouseCancer researchmedicineImmunohistochemistryPhysical and Theoretical ChemistryMolecular BiologySpectroscopyEx vivoInternational Journal of Molecular Sciences
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Histological features and ki-67 index in cervical atypical lesions

2008

One of the most frequent challenges in routine diagnostic assessment of cervical biopsies consists of some lesions in which histological features of HPV infection are either inconsistently present or only mildly/focally evident. We named them Atypical Lesions (AL) because differential diagnosis with metaplastic/reactive lesions and LSIL is difficult. It would be important to identify among them those lesions that are really HPV-associated. We studied 52 AL cases to evaluate whether the morphological features and the proliferation index, assessed by Mib1 (Ki67) immunostaining, would be useful to better understand the real nature of AL, with relation to the HPV presence and to the proliferati…

Univariate analysisPathologymedicine.medical_specialtyProliferation indexHPV PositiveHPV koilocytosis Mib1PCRHPV infectionBiologymedicine.diseaseKoilocyteInfectious DiseasesKi-67medicinebiology.proteinDifferential diagnosisImmunostaining
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New Sperm Morphology Analysis in Equids : Trumorph ® Vs Eosin-Nigrosin Stain

2021

Equine Reproduction Service. Department of Animal Medicine and Surgery. Veterinary Faculty. Autonomous University of Barcelona. National Agency for Research and Development (ANID), Ministry of Education, Chile (2017/72180128). Secretary of Higher Education, Science, Technology and Innovation (SENESCYT)(CZ02-000507-2019) The evaluation of the male fertility potential is based on the analysis of the basic spermatic characteristics of concentration, motility and morphology. Thus, the study of sperm morphology is a fundamental element in the seminal analysis, but its real meaning has been biased by the techniques used for its evaluation. These techniques involve dehydration phases and subsequen…

Veterinary medicineSperm morphologySemenBiologyTrumorph ®HorseStainSemen collectiondonkeyAndrology03 medical and health scienceschemistry.chemical_compound0302 clinical medicineEosin-nigrosin stainDonkeySF600-1100Trumorph<sup>®</sup>030219 obstetrics & reproductive medicineGeneral VeterinaryEosinsperm morphologyurogenital systemAses -- Espermatozoides0402 animal and dairy sciencehorse; donkey; sperm morphology; eosin-nigrosin stain; Trumorph<sup>®</sup>04 agricultural and veterinary sciences040201 dairy & animal scienceSpermStaininghorseNigrosinchemistryeosin-nigrosin stainSperm morphologyAses
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PML nuclear body-residing proteins sequentially associate with HPV genome after infectious nuclear delivery.

2019

Subnuclear promyelocytic leukemia (PML) nuclear bodies (NBs) are targeted by many DNA viruses after nuclear delivery. PML protein is essential for formation of PML NBs. Sp100 and Small Ubiquitin-Like Modifier (SUMO) are also permanently residing within PML NBs. Often, large DNA viruses disassemble and reorganize PML NBs to counteract their intrinsic antiviral activity and support establishment of infection. However, human papillomavirus (HPV) requires PML protein to retain incoming viral DNA in the nucleus for subsequent efficient transcription. In contrast, Sp100 was identified as a restriction factor for HPV. These findings suggested that PML NBs are important regulators of early stages o…

Viral DiseasesPhysiologyvirusesIntranuclear Inclusion BodiesPromyelocytic Leukemia ProteinVirus ReplicationBiochemistryAutoantigensImmune PhysiologyMedicine and Health SciencesCell Cycle and Cell DivisionNuclear proteinBiology (General)PapillomaviridaeStaining0303 health sciencesViral GenomicsImmune System ProteinsChromosome Biology030302 biochemistry & molecular biologyCell StainingTotal Cell CountingNuclear Proteinsvirus diseasesAntigens NuclearGenomicsCell biologymedicine.anatomical_structureInfectious DiseasesCapsidCell ProcessesViral GenomeCellular Structures and OrganellesIntranuclear SpaceResearch ArticleHuman Papillomavirus InfectionQH301-705.5UrologyImmunologyCell Enumeration TechniquesSUMO-1 ProteinSexually Transmitted DiseasesMitosisMicrobial GenomicsGenome ViralBiologyResearch and Analysis MethodsMicrobiologyVirusAntibodies03 medical and health sciencesPromyelocytic leukemia proteinVirologyNuclear BodiesmedicineGeneticsHumansVesiclesMolecular BiologyMitosisTranscription factor030304 developmental biologyCell NucleusGenitourinary InfectionsTumor Suppressor ProteinsBiology and Life SciencesProteinsCell BiologyRC581-607Cell nucleusViral replicationSpecimen Preparation and Treatmentbiology.proteinParasitologyCapsid ProteinsImmunologic diseases. AllergyTranscription FactorsPLoS Pathogens
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Evaluation of the effect of different enamel surface treatments and waiting times on the staining prevention after bleaching

2017

Background Bleached dental enamel can be more susceptible to staining than the enamel that has never been bleached, especially right after tooth bleaching. The aim of this study is to evaluate the effect of surface treatments and waiting time prior to contact with dye on bleached enamel staining susceptibility. Material and Methods One hundred teeth were bleached with 35% hydrogen peroxide (Whiteness HP, FGM) and randomly assigned to G1 artificial saliva, G2 2% sodium fluoride (Flugel, Nova DFL), G3 casein phosphopeptide-amorphous calcium phosphate fluoride paste (CPP-ACPF, MI Paste Plus, GC America), G4 rinse for color maintenance after bleaching (Keep White Rinse, DMC) and G5 polishing wi…

Waiting timeSalivagenetic structuresColorDentistry01 natural sciences010309 optics03 medical and health scienceschemistry.chemical_compound0302 clinical medicinestomatognathic system0103 physical sciencesSodium fluorideDental enamelHydrogen peroxideGeneral DentistryWineEnamel paintPigmentationbusiness.industryResearchEsthetic Dentistry030206 dentistry:CIENCIAS MÉDICAS [UNESCO]Hydrogen peroxideStainingstomatognathic diseaseschemistryvisual_artUNESCO::CIENCIAS MÉDICASvisual_art.visual_art_mediumTooth bleachingsense organsbusinessFluorideJournal of Clinical and Experimental Dentistry
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