Search results for "fluorescent"

showing 10 items of 863 documents

Bārija borātu sintēze ūdens šķīdumos un to raksturojums

2019

Bārija borātu sintēze ūdens šķīdumos un to raksturojums. Čerpakovska Z., bakalaura darba vadītājs Dr. ķīm., asoc. prof. Švirksts J. Bakalaura darbs, 58 lappuses, 14 attēli, 9 tabulas, 67 literatūras avoti, 4 pielikumi. Latviešu valodā. Darbā veikta bārija borātu BaxByOz∙nH2O sintēze, izmantojot bārija hlorīda, bārija hidroksīda, bārija nitrāta, borskābes, dinātrija tetraborāta, nātrija metaborāta, kālija hidroksīda, nātrija hidroksīda, amonjaka šķīdumus. Iegūtie savienojumi raksturoti ar pulvera rentgenstaru difraktometrijas, rentgenfluorescentās spektrometrijas, termiskās analīzes, Furjē tranformāciju infrasarkanās spektrometrijas un titrimetrijas metodēm.

KRISTĀLISKIE BĀRIJA BORĀTIAMORFIE BĀRIJA BORĀTIRENTGENSTARFLUORESCENTĀ SPEKTROMETRIJATERMISKĀ ANALĪZEPULVERA RENTGENSTARU DIFRAKTOMETRIJAĶīmija
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Subcellular Localization of β-Catenin Is Regulated by Cell Density

2002

It is generally accepted that subcellular distribution of beta-catenin regulates its function. Membrane-bound beta-catenin mediates cell-cell adhesion, whereas elevation of the cytoplasmic and nuclear pool of the protein is associated with an oncogenic function. Although the role of beta-catenin in transformed cells is relatively well characterized, little is known about its importance in proliferation and cell-cycle control of nontransformed epithelial cells. Using different approaches we show that in human keratinocytes (HaCaT) beta-catenin is distributed throughout the cells in subconfluent, proliferating cultures. In contrast, beta-catenin is nearly exclusively located at the plasma mem…

KeratinocytesBiophysicsBiologyBiochemistryCell LineHumansFluorescent Antibody Technique IndirectMolecular Biologybeta CateninContact InhibitionCell MembraneContact inhibitionCell BiologyAdhesionCadherinsSubcellular localizationCell biologyCytoskeletal ProteinsKineticsProtein TransportHaCaTMembraneDesmoplakinsCytoplasmCateninTrans-ActivatorsCell DivisionFunction (biology)Biochemical and Biophysical Research Communications
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Shuttling of the autoantigen La between nucleus and cell surface after uv irradiation of human keratinocytes.

1990

During the past years we have established that the nuclear autoantigen La shuttles between the nucleus and the cytoplasm in tumor cells after inhibition of transcription or virus infection. We reinvestigated this shuttling using primary human keratinocytes from both healthy donors and patients with xeroderma pigmentosum. Ultraviolet irradiation resulted in both an inhibition of transcription and a translocation of La protein from the nucleus to the cytoplasm. After a prolonged inhibition of transcription La protein relocated into the nucleus and assembled with nuclear storage regions. The uv-induced shuttling included a translocation to the cell surface, where La protein colocalized with ep…

KeratinocytesCytoplasmTranscription GeneticUltraviolet RaysCellFluorescent Antibody TechniqueBiologyAutoantigensTranscription (biology)Epidermal growth factormedicineHumansNuclear proteinCell NucleusEpidermal Growth FactorCell MembraneBiological TransportCell BiologyCell biologyErbB ReceptorsCell nucleusmedicine.anatomical_structureBiochemistryRibonucleoproteinsCytoplasmProtein BiosynthesisKeratinocyteNucleusExperimental cell research
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Epigenetic control of IL-23 expression in keratinocytes is important for chronic skin inflammation

2018

The chronic skin inflammation psoriasis is crucially dependent on the IL-23/IL-17 cytokine axis. Although IL-23 is expressed by psoriatic keratinocytes and immune cells, only the immune cell-derived IL-23 is believed to be disease relevant. Here we use a genetic mouse model to show that keratinocyte-produced IL-23 is sufficient to cause a chronic skin inflammation with an IL-17 profile. Furthermore, we reveal a cell-autonomous nuclear function for the actin polymerizing molecule N-WASP, which controls IL-23 expression in keratinocytes by regulating the degradation of the histone methyltransferases G9a and GLP, and H3K9 dimethylation of the IL-23 promoter. This mechanism mediates the inducti…

KeratinocytesMale0301 basic medicinemedicine.medical_treatmentWiskott-Aldrich Syndrome Protein NeuronalGeneral Physics and AstronomyEpigenesis GeneticHistonesMice0302 clinical medicineGenes ReporterInterleukin 23Promoter Regions Geneticlcsh:ScienceSkinMice KnockoutMultidisciplinaryInterleukin-17QMiddle AgedCytokine030220 oncology & carcinogenesisHistone methyltransferaseTumor necrosis factor alphaSignal transductionmedicine.symptomSignal TransductionAdultScienceGreen Fluorescent ProteinsPrimary Cell CultureInflammationBiologyArticleGeneral Biochemistry Genetics and Molecular Biology03 medical and health sciencesImmune systemPsoriasismedicineAnimalsHumansPsoriasisInflammationHistone-Lysine N-MethyltransferaseGeneral Chemistrybiochemical phenomena metabolism and nutritionmedicine.diseaseDisease Models AnimalHEK293 Cells030104 developmental biologyInterleukin-23 Subunit p19Cancer researchlcsh:QNature Communications
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Pore-forming Staphylococcus aureus alpha-toxin triggers epidermal growth factor receptor-dependent proliferation.

2006

Staphylococcal alpha-toxin is an archetypal killer protein that homo-oligomerizes in target cells to create small transmembrane pores. The membrane-perforating beta-barrel motif is a conserved attack element of cytolysins of Gram-positive and Gram-negative bacteria. Following the recognition that nucleated cells can survive membrane permeabilization, a profile of abundant transcripts was obtained in transiently perforated keratinocytes. Several immediate early genes were found to be upregulated, reminiscent of the cellular response to growth factors. Cell cycle analyses revealed doubling of S + G2/M phase cells 26 h post toxin treatment. Determination of cell counts uncovered that after an …

KeratinocytesStaphylococcus aureusSrc Homology 2 Domain-Containing Transforming Protein 1ImmunologyCellBacterial ToxinsBlotting WesternFluorescent Antibody TechniqueTransfectionMicrobiologyCell LineHemolysin ProteinsDownregulation and upregulationNucleated cellVirologymedicineHumansGrowth factor receptor inhibitorEpidermal growth factor receptorStaphylococcus aureus alpha toxinAdaptor Proteins Signal TransducingCell Line TransformedCell ProliferationbiologyCytotoxinsReverse Transcriptase Polymerase Chain ReactionGene Expression ProfilingCell CycleCell cycleFlow CytometryTransmembrane proteinCell biologyErbB Receptorsmedicine.anatomical_structureShc Signaling Adaptor Proteinsbiology.proteinMitogensSignal TransductionCellular microbiology
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Amyloid P component--a special type of collagen?

1978

The localization of amyloid P-components is demonstrated by immunofluorescence microscopy in normal human tissue (kidney, spleen, liver). The relation to collagen and to amyloidosis is discussed.

KidneyPathologymedicine.medical_specialtyAmyloidAmyloidChemistryAmyloidosisGoatsImmune SeraFluorescent Antibody TechniqueSpleenImmunofluorescence MicroscopyMiddle Agedmedicine.diseaseKidneyPathology and Forensic MedicineAmyloid P ComponentCollagen type I alpha 1medicine.anatomical_structureLivermedicineAnimalsHumansCollagenSpleenVirchows Archiv. B, Cell pathology
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Kininogen binding protein p33/gC1qR is localized in the vesicular fraction of endothelial cells

1996

AbstractThe endothelial protein p33/gC1qR is thought to mediate the assembly of components of the kinin-forming and complement-activating pathways on the surface of cardiovascular cells. FACS analysis of intact human umbilical vein endothelial cells using specific antibodies to p33 revealed a minor fluorescence on the cell surface whereas permeabilized cells showed a bright fluorescence indicative of an intracellular localization of p33. Immunostaining of fixed cells confirmed the predominant intracellular localization of p33. Fractionation studies demonstrated that the vesicular but not the membrane fraction of EA.hy926 cells is rich in p33. We conclude that externalization of p33 must pre…

Kininogen bindingp33Kininogen binding proteinCellBiophysicsComplementFluorescent Antibody TechniqueBiologyBiochemistryUmbilical veinMitochondrial ProteinsStructural BiologyGeneticsmedicineHumansMolecular BiologyCells CulturedMembrane GlycoproteinsImmune SeraCell BiologyKininFlow CytometryKininFluorescenceReceptors ComplementCell biologyEndothelial stem cellSpecific antibodyHyaluronan Receptorsmedicine.anatomical_structuregC1qREndothelium VascularCarrier ProteinsImmunostainingFEBS Letters
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Autoantibody detection using indirect immunofluorescence on HEp-2 cells

2009

The detection of autoantibodies is an important element in the diagnosis and monitoring of disease progression in patients with autoimmune diseases. In laboratory diagnostic tests for connective tissue and autoimmune liver diseases, indirect immunofluorescence on HEp-2 cells plays a central role in a multistage diagnostic process. Despite the high quality of diagnostics, findings at different laboratories can differ considerably due to a lack of standardization, as well as subjective factors. The present paper formulates recommendations for the standardized processing and interpretation of the HEp-2 cell test for the detection of non-organ-specific (especially antinuclear) antibodies. It pr…

Laboratory ProcedureAnti-nuclear antibodymedicine.disease_causeImmunofluorescenceGeneral Biochemistry Genetics and Molecular BiologyAutoimmunityHistory and Philosophy of ScienceCell Line TumormedicineHumansFluorescent Antibody Technique IndirectAutoantibodiesbiologymedicine.diagnostic_testbusiness.industryGeneral NeuroscienceAutoantibodyReproducibility of ResultsReference StandardsLaboratory quality controlTiterAntibodies AntinuclearImmunologybiology.proteinAntibodybusiness
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Inhibition of lactate export by quercetin acidifies rat glial cells in vitro

1997

The relationship between glial lactate release and glial intracellular pH (pH i) regulation is studied using C6 glioma cells and rat astrocytes in vitro, and the lactate transport inhibitors quercetin and a-cyano-4-hydroxycinnamate (CHC). pHi is measured using 2′,7′bis(carboxyethyl)-5,6-carboxyfluorescein (BCECF). The results show that lactate release is mediated partly by a specific lactate transport system inhibitable by quercetin (50 mM), but not by CHC (5 mM). Inhibition by quercetin results in a significant 3‐4-fold increase of intracellular lactate and a decrease of intracellular pH to 6.9. A participation of quercetin-inhibitable lactate transport in glial pHi-regulation is suggested…

Lactate transportIntracellular pHBiologychemistry.chemical_compoundTumor Cells CulturedmedicineAnimalsheterocyclic compoundsLactic AcidFluorescent DyesGeneral NeuroscienceBiological TransportHydrogen-Ion ConcentrationFluoresceinsIn vitroRatsLactic acidmedicine.anatomical_structurechemistryBiochemistryCell cultureNeurogliaQuercetinQuercetinAcidsNeurogliaIntracellularNeuroscience Letters
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Lanthanide complexes as imaging agents anchored on nano-sized particles of boehmite

2011

International audience; The synthesis of boehmite nanoparticles modified with lanthanides (Eu, Tb and Gd) is described. Their synthesis, characterization and in vitro assays with HeLa cells were performed. The nuclear magnetic relaxation dispersion (NMRD) profiles of the two chelating moieties were studied. Imaging data from laser scanning confocal fluorescence microscopy and flow cytometry revealed that the nanoscaffolds were taken up by the cells, distributed throughout the cytoplasm and showed no toxicity. This platform could represent an alternative to silica-based inert matrices as imaging vehicles.

LanthanideBoehmiteGADOLINIUM(III) COMPLEXESRELAXIVITYConfocalEUROPIUMchemistry.chemical_elementNanoparticleMetal NanoparticlesAluminum Hydroxide02 engineering and technology010402 general chemistry01 natural sciencesLanthanoid Series ElementsPROBESInorganic ChemistryCoordination ComplexesMicroscopyFluorescence microscopeAluminum OxideNANOPARTICLESHumans[CHIM]Chemical SciencesParticle SizeCYCLEN COMPLEXESFluorescent DyesMicroscopy ConfocalMRI CONTRAST AGENTS021001 nanoscience & nanotechnologyFlow Cytometry0104 chemical scienceschemistryWATER-EXCHANGELUMINESCENCE0210 nano-technologyEuropiumLuminescenceEMISSIONNuclear chemistryHeLa Cells
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