Search results for "Fluorescence"

showing 10 items of 2463 documents

α-casein micelles-membranes interaction: Flower-like lipid protein coaggregates formation

2022

Background: Environmental conditions regulate the association/aggregation states of proteins and their action in cellular compartments. Analysing protein behaviour in presence of lipid membranes is fundamental for the comprehension of many functional and dysfunctional processes. Here, we present an experimental study on the interaction between model membranes and α-casein. α-casein is the major component of milk proteins and it is recognised to play a key role in performing biological functions. The conformational properties of this protein and its capability to form supramolecular structures, like micelles or irreversible aggregates, are key effectors in functional and pathological effects…

MembranesCaseinBiophysicsRICSCaseinsMilk ProteinsLipidsMolecular BiologyBiochemistryFluorescenceSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)MicellesProtein-membrane interactionsBiochimica et Biophysica Acta (BBA) - General Subjects
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Flow cytometry, sorting and immunocharacterization with proliferating cell nuclear antigen of cycling and non-cycling cells in synchronized pea root …

1997

In the 3-d-old 2-mm root tip of Pisum sativum L. cv. Lincoln the percentage of actively proliferating cells is estimated to be 70%. The remaining cells are non-cycling and arrested with 2C and 4C DNA content in G0 and in G2Q, respectively. In this work we studied the kinetic significance of these quiescent cells, using the sorting capabilities of flow cytometry and immunofluorescence techniques to detect the proliferation marker PCNA (proliferating cell nuclear antigen) inside cells within the different cell-cycle compartments. While in animal cells, PCNA is present at a high level only in actively proliferating cells, in 3-d-old pea root tips 95% of the cells are PCNA-positive. After flow …

MeristemPlant ScienceBiologyImmunofluorescencePlant RootsPisumFlow cytometryProliferating Cell Nuclear AntigenGeneticsmedicineHydroxyureaProliferation MarkerFluorescent Antibody Technique IndirectRoot capCell Nucleusmedicine.diagnostic_testCell CyclePeasMicrotomyCell cycleMeristemFlow Cytometrybiology.organism_classificationProliferating cell nuclear antigenCell biologybiology.proteinPlanta
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Live imaging of stem cell and progeny behaviour in physiological hair-follicle regeneration

2012

Tissue development and regeneration depend on cell-cell interactions and signals that target stem cells and their immediate progeny. However, the cellular behaviours that lead to a properly regenerated tissue are not well understood. Using a new, non-invasive, intravital two-photon imaging approach we study physiological hair-follicle regeneration over time in live mice. By these means we have monitored the behaviour of epithelial stem cells and their progeny during physiological hair regeneration and addressed how the mesenchyme influences their behaviour. Consistent with earlier studies, stem cells are quiescent during the initial stages of hair regeneration, whereas the progeny are more …

MesodermCell divisionCell SurvivalMesenchymeMice TransgenicBiologyArticleMesodermMiceCell MovementStem CellLive cell imagingmedicineAnimalsRegenerationMultidisciplinaryintegumentary systemAnimalStem CellsMedicine (all)Regeneration (biology)DermisHair follicleCell biologyMicroscopy Fluorescence Multiphotonmedicine.anatomical_structureAnimals; Cell Division; Cell Movement; Cell Survival; Cell Tracking; Dermis; Hair Follicle; Laser Therapy; Mesoderm; Mice; Mice Transgenic; Microscopy Fluorescence Multiphoton; Regeneration; Stem Cells; Medicine (all); MultidisciplinaryCell TrackingDermiLaser TherapyStem cellHair FollicleDevelopmental biologyCell DivisionNature
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Long-Lived Luminescence and Slow Carrier Diffusion in Metal Halide Perovskites as a result of Multiple Trapping and De-Trapping by Shallow Non-Quench…

2018

MetalQuenching (fluorescence)Materials scienceChemical physicsvisual_artvisual_art.visual_art_mediumHalideTrappingDiffusion (business)LuminescenceProceedings of the nanoGe Fall Meeting 2018
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Synthesis and antibacterial activity of iron-hexacyanocobaltate nanoparticles.

2018

This paper deals with the synthesis and characterization of iron-hexacyanocobaltate (FeHCC) and its antibacterial properties. The nanoparticles were prepared by a facile co-precipitation technique. Crystal structure, particle morphology, and elemental composition were determined using X-ray Powder Diffraction, X-ray fluorescence spectroscopy, Transmission Electron Microscopy (TEM), and Infrared Spectroscopy (IR). The antibacterial activity of the FeHCC nanoparticles was tested against Escherichia coli and Staphylococcus aureus as models for Gram-negative and Gram-positive bacteria, respectively, by bacterial counting method and microscopic visualization (TEM, FEG-SEM, and fluorescence micro…

Metal-hexacyanoferrateStaphylococcus aureusIronColony Count MicrobialInfrared spectroscopyNanoparticleMetal Nanoparticles02 engineering and technologyMicrobial Sensitivity TestsBacterial growth010402 general chemistrymedicine.disease_cause01 natural sciencesBiochemistryFluorescence spectroscopyInorganic ChemistryMicroscopy Electron TransmissionmedicineFluorescence microscopeEscherichia coliEscherichia coliCyanidesChemistryIron-hexacyanocobaltateCobalt021001 nanoscience & nanotechnology0104 chemical sciencesAnti-Bacterial AgentsSpectrometry FluorescenceStaphylococcus aureuMicroscopy Electron ScanningAntibacterial activity0210 nano-technologyAntibacterial activityReactive Oxygen SpeciesNuclear chemistryMacromoleculeJournal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry
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Group-specific quantification of methanotrophs in landfill gas-purged laboratory biofilters by tyramide signal amplification-fluorescence in situ hyb…

2008

The aim of this study was to quantitatively analyse methanotrophs in two laboratory landfill biofilters at different biofilter depths and at temperatures which mimicked the boreal climatic conditions. Both biofilters were dominated by type I methanotrophs. The biofilter depth profiles showed that type I methanotrophs occurred in the upper layer, where relatively high O(2) and low CH(4) concentrations were present, whereas type II methanotrophs were mostly distributed in the zone with high CH(4) and low O(2) concentrations. The number of type I methanotrophic cells declined when the temperature was raised from 15 degrees C to 23 degrees C, but increased when lowered to 5 degrees C. A slight …

MethanobacteriaceaeEnvironmental EngineeringType I methanotrophsBioengineeringmedicineWaste Management and DisposalIn Situ Hybridization FluorescenceDNA PrimersType II methanotrophsmedicine.diagnostic_testBase SequenceRenewable Energy Sustainability and the EnvironmentChemistryEnvironmental engineeringGeneral MedicineAmidesRefuse DisposalLandfill gasEnvironmental chemistrySoil waterAnaerobic oxidation of methaneBiofilterGasesOligonucleotide ProbesSignal amplificationFiltrationFluorescence in situ hybridizationBioresource technology
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Procedure for the Screening of Eggs and Egg Products to Detect Oxolonic Acid, Ciprofloxacin, Enrofloxacin, and Sarafloxacin Using Micellar Liquid Chr…

2019

A method based on micellar liquid chromatography was developed to determine oxolinic acid, ciprofloxacin, enrofloxacin, and sarafloxacin in eggs and egg products. The antimicrobial drugs were obtained in a micellar solution which was directly injected. The analytes were resolved using a C18 column and a mobile phase of 0.05 M sodium dodecyl sulfate—7.5% 1-propanol—0.5% triethylamine, buffered at pH 3 with phosphate salt, running under the isocratic mode. The signal was monitored by fluorescence. Validation was successfully performed according to the EU Commission Decision 2002/657/EC in terms of specificity, calibration range (LOQ to 1 mg/kg), linearity (R2 &gt

Microbiology (medical)Analytelaying hen01 natural sciencesBiochemistryMicrobiologyArticlechemistry.chemical_compoundSarafloxacinOxolinic acidEnrofloxacinmedicinePharmacology (medical)General Pharmacology Toxicology and PharmaceuticsTriethylamineDetection limitvalidationResidue (complex analysis)Chromatography010405 organic chemistryChemistry010401 analytical chemistrylcsh:RM1-950solid-to-liquid extraction0104 chemical sciencesfood safetyInfectious Diseaseslcsh:Therapeutics. PharmacologyMicellar liquid chromatographyfluorescenceoptimizationmedicine.drugAntibiotics
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Selective growth-inhibitory effect of 8-hydroxyquinoline towards Clostridium difficile and Bifidobacterium longum subsp. longum in co-culture analyse…

2014

The major risk factor for Clostridium difficile infection (CDI) is the use of antibiotics owing to the disruption of the equilibrium of the host gut microbiota. To preserve the beneficial resident probiotic bacteria during infection treatment, the use of molecules with selective antibacterial activity enhances the efficacy by selectively removing C. difficile. One of them is the plant alkaloid 8-hydroxyquinoline (8HQ), which has been shown to selectively inhibit clostridia without repressing bifidobacteria. Selective antimicrobial activity is generally tested by culture techniques of individual bacterial strains. However, the main limitation of these techniques is the inability to describe …

Microbiology (medical)Bifidobacterium longumbiologymedicine.diagnostic_testClostridioides difficilemedicine.drug_classAntibioticsGeneral MedicineClostridium difficileGut floraFlow CytometryOxyquinolinebiology.organism_classificationAntimicrobialMicrobiologyAnti-Bacterial AgentsFlow cytometryMicrobiologyClostridiamedicineMicrobial InteractionsBifidobacteriumAntibacterial activityIn Situ Hybridization FluorescenceJournal of Medical Microbiology
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Relationship between the target antigen of liver-kidney microsomal (LKM) autoantibodies and rat isoenzymes of cytochrome P-450

1988

Chronic active hepatitis (CAH) is a clinical syndrome of different etiologies. Liver-kidney microsomal (LKM) autoantibodies characterize a subgroup of HBsAg negative CAH, which is considered to be an autoimmune liver disease. By immunoblotting analysis (IB) LKM positive sera have been shown to react strongly with a poly-peptide band at 50 kD. Therefore we investigated various rat microsomal enzymes with a molecular weight around 50 kD as potential candidate target antigens. These included epoxide hydrolase, cytochrome P-450 reductase, and phenobarbital-inducible isoenzymes of cytochrome P-450 (PB1, PB2, PB3a, PB3b). By radioimmunoassay (RIA) and IB LKM positive sera were shown to react with…

Microbiology (medical)Cytochromebiologymedicine.diagnostic_testBiochemistry (medical)Clinical BiochemistryPublic Health Environmental and Occupational HealthAutoantibodyHematologyReductaseImmunofluorescenceMolecular biologyEpitopeMedical Laboratory TechnologyAntigenBiochemistrybiology.proteinmedicineMicrosomeImmunology and AllergyEpoxide hydrolaseJournal of Clinical Laboratory Analysis
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Methodology and significance of the detection of liver-kidney-microsomal (lkm) autoantibodies in autoimmune-type chronic active hepatitis

1987

Liver-kidney-microsomal (LKM) autoantibodies are diagnostic markers for a subgroup of HBsAg-negative chronic active hepatitis, presumably owing to autoimmunity. They were originally detected by indirect immunofluorescence and can now be evaluated by radioimmunoassay, enzyme-linked immunosorbent assay, and immunoblotting. In immunoblotting LKM-positive sera react strongly with a 50-kilodalton (KD) polypeptide band of microsomes. In immunoelectron microscopy, LKM-positive sera show a binding with membranes of the endoplasmic reticulum. The LKM antigen was further identified on various isoenzymes of cytochrome P-450. Immunofluorescence is still the method of choice for screening sera routinely…

Microbiology (medical)HepatitisPathologymedicine.medical_specialtyCirrhosismedicine.diagnostic_testImmunoelectron microscopyBiochemistry (medical)Clinical BiochemistryPublic Health Environmental and Occupational HealthAutoantibodyRadioimmunoassayHematologyBiologymedicine.diseasemedicine.disease_causeImmunofluorescenceAutoimmunityMedical Laboratory TechnologyAntigenImmunologymedicineImmunology and AllergyJournal of Clinical Laboratory Analysis
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