Search results for "Fluorescence"

showing 10 items of 2463 documents

OPTICAL SENSING OF POLLUTANTS BY FLUORESCENT CARBON NANODOTS

2022

Settore FIS/01 - Fisica SperimentaleCARBON NANODOTS FLUORESCENCE SENSING
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Ultrafast broadband fluorescnce up-conversion of N-acetyl-L-tryptophanamide (NATA)

2011

Settore FIS/01 - Fisica SperimentaleTryptophan fluorescence upconversion ultrafast solvation hydrogen bonding
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MIXING TIME IN UNBAFFLED STIRRED TANKS

2012

Unbaffled stirred tanks, despite their poorer mixing performance with respect to baffled vessels, are gaining a growing industrial interest as they provide significant advantages in selected applications, including a number of biochemical, food and pharmaceutical processes. There still is however a general lack of information on their mixing performance, that needs to be addressed in order to fully exploit their application potential. The present work is aimed at providing experimental information on mixing rates in an unbaffled vessel operated without top-cover (Uncovered Unbaffled Stirred Tank, UUST). The planar laser induced fluorescence (PLIF) technique was adopted for measuring the dis…

Settore ING-IND/25 - Impianti ChimiciMixing time unbaffled stirred tanks planar laser induced fluorescence PLIF
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Techniques to evaluate erythrocyte deformability in diabetes mellitus

2005

Using several rheological techniques, we examined the erythrocyte deformability in different groups of diabetic subjects. The macrorheological techniques used for this evaluation were respectively whole-blood filtration, filtration of erythrocyte suspensions, polyviscosimetry and diffractometry. Whole-blood filterability, at a negative pressure of 20 cm water, was decreased in type 2 diabetics; no difference was evident at a negative pressure of 10 cm water. The filtration of erythrocyte suspensions at low haematocrit (5%) did not show differences between normal and diabetic subjects. The polyviscosimetry, which explores the filterability of erythrocyte suspensions at high haematocrit (80%)…

Settore MED/09 - Medicina InternaEndocrinology Diabetes and MetabolismHematocritFluorescence spectroscopypolyviscosimetrylaw.inventionEndocrinologyReference ValueslawErythrocyte DeformabilityDiabetes mellitusDiabetes MellitusInternal MedicinemedicineHumansErythrocyte deformabilityLaser beamsFiltrationwhole-blood filtrationmedicine.diagnostic_testdiabetes mellituViscosityChemistryErythrocyte MembraneGeneral Medicinemedicine.diseaseRed cell membraneDiabetes Mellitus Type 1MembraneDiabetes Mellitus Type 2HematocritBiochemistryerythrocyte filtrationBiophysicsdiffractometryerythrocyte membrane dynamic propertieActa Diabetologica
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Potentialgesteuerte SS-Bindungsspaltung und Fluoreszenzmarkierungsstudien am Beispiel des Rinderinsulins

1985

Die drei SS-Brucken im Insulin konnen galvanostatisch unter Bildung der SH-A-Kette und der SH-B-Kette (Produktgemisch I) aufgespalten werden. Potentiostatisch gelingt bei -1.3 V (vs. SCE) die selektive Offnung der zwei interchenaren Disulfidbrucken (Produktgemisch II). Die vier SH-Gruppen im Produktgemisch II werden mit dem Vinylsulfon 1 blockiert (Produktgemisch III). Im Produktgemisch III wird die intrachenare Disulfidbrucke in der teilblockierten A-Kette bei -1.8 V (vs. SCE) potentiostatisch reduktiv geoffnet und mit dem fluoreszierenden Arylvinylsulfon 2 geschutzt (Produktgemisch IV). Auch die SH-Gruppen in den Produktgemischen I und II werden durch die fluoreszierenden Vinylsulfone 2 u…

Sh groupschemistry.chemical_compoundChemistryReductive cleavageArylOrganic ChemistryPolymer chemistryPhysical and Theoretical ChemistryVinyl sulfoneCleavage (embryo)FluorescenceLiebigs Annalen der Chemie
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Gezielte und reversible Fluoreszenzmarkierung von SH-Lysozym mit Vinylsulfonen

1985

Am Beispiel von SH-Lysozym wird gezeigt, wie man SH-Gruppen reversibel mit den Vinylsulfonen 1–4 nach Gl. (a) selektiv blockieren und nach Gl. (b) selektiv deblockieren kann. Das wasserlosliche Vinylsulfon 2 macht das blockierte SH-Lysozym wasserloslich. Durch Einwirkung von NaOH-Losung wird nach Gl. (b) das wasserunlosliche SH-Lysozym regeneriert. Die fluoreszierenden Vinylsulfone 3 und 4 konnen als Fluoreszenzmarker nach verschiedenen Arbeitsweisen zum qualitativen Nachweis und zur quantitativen Bestimmung von SH-Gruppen herangezogen werden. Selective and Reversible Fluorescence Marking of SH-Lysozyme with Vinyl Sulfones The SH groups of SH-lysozyme as a model substance are selectively bl…

Sh groupschemistry.chemical_compoundChemistrySodium hydroxideOrganic ChemistryPolymer chemistryPhysical and Theoretical ChemistryVinyl sulfoneFluorescenceLiebigs Annalen der Chemie
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Electron transfer mechanism in Shewanella loihica PV-4 biofilms formed at graphite electrode

2012

Abstract Electron transfer mechanisms in Shewanella loihica PV-4 viable biofilms formed at graphite electrodes were investigated in potentiostat-controlled electrochemical cells poised at oxidative potentials (0.2 V vs. Ag/AgCl). Chronoamperometry (CA) showed a repeatable biofilm growth of S. loihica PV-4 on graphite electrode. CA, cyclic voltammetry (CV) and its first derivative shows that both direct electron transfer (DET) mediated electron transfer (MET) mechanism contributes to the overall anodic (oxidation) current. The maximum anodic current density recorded on graphite was 90 μA cm − 2 . Fluorescence emission spectra shows increased concentration of quinone derivatives and riboflavi…

ShewanellaElectroactive biofilmBioelectric Energy SourcesExtracellular Electron TransferRiboflavinInorganic chemistryBiophysicsElectrochemical cellElectron TransportElectron transferGraphite electrodeElectrochemistryGraphitePhysical and Theoretical ChemistryElectrodesMicroscopy ConfocalChemistryQuinonesBiofilmmediated electron transferElectrochemical TechniquesGeneral MedicineChronoamperometryAnodeSpectrometry FluorescenceShewanella loihica PV- 4Extracellular Electron Transfer; Shewanella loihica PV- 4; Electroactive biofilms; Graphite electrode; mediated electron transferBiofilmsMicroscopy Electron ScanningGraphiteDifferential pulse voltammetryCyclic voltammetryOxidation-ReductionBioelectrochemistry
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Accretion shock on CTTSs and its X-ray emission

2009

High spectral resolution X-ray observations of classical T Tauri stars (CTTSs) demonstrate the presence of plasma at T~2-3×10^6 K and ne~10^11-10^13 cm-3. Stationary models suggest that this emission is due to shock-heated accreting material. We address this issue by a 1-D hydrodynamic model of the impact of the accretion flow onto a chromosphere of a CTTS with the aim of investigating the stability of accretion shock and the role of the chromosphere. Our simulations include the effects of gravity, radiative losses from optically thin plasma, the thermal conduction and a detailed modeling of the stellar chromosphere. Here we present the results of a simulation based on the parameters of the…

Shock wavePhysicsPlanetary bow shocksAstrophysics::High Energy Astrophysical Phenomenainterplanetary shocksPlasmaAstrophysicsNumerical approximation and analysisThermal conductionAccretion (astrophysics)T Tauri starSettore FIS/05 - Astronomia E AstrofisicaX-ray emission spectra and fluorescenceRadiative transferHydrodynamicsAstrophysics::Solar and Stellar AstrophysicsAstrophysics::Earth and Planetary AstrophysicsSpectral resolutionChromosphereAstrophysics::Galaxy Astrophysics
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Morphological distribution of μ chains and cd15 receptors in colorectal polyp and adenocarcinoma specimens

2013

BACKGROUND: We have recently investigated the localisation of immunoglobulin-producing cells (IPCs) in inflamed intestinal tissue samples from patients with inflammatory bowel disease (IBD), and identified two main patterns of B lymphocyte infiltration: one characterised by the moderate strong stromal localisation of small B1 cell-like IgM+/CD79+/CD20-/CD21-/CD23-/CD5 ± IPCs, and the other by the peri-glandular localisation of IPCs with irregular nuclei that had surface markers specific for a B cell subset (IgM and CD79), but quantitative differences in their λ and κ chains. The same patients were also tested for CD15+ receptors, which were localised on inflammatory cell surfaces or in the …

Sialyl-LewisXPathologymedicine.medical_specialtyHistologyStromal cellCD792734B-1 cells; Colorectal adenocarcinoma; Inflammatory bowel disease; Matrix metalloproteinases; Sialyl-LewisX; 2734; HistologyCell morphologyImmunofluorescencecolorectal polyp and adenocarcinomaInflammatory bowel diseaseColorectal adenocarcinomaPathology and Forensic MedicineB-1 cellsmedicineReceptorB cellImmunoperoxidasemedicine.diagnostic_testbusiness.industrymedicine.diseaseMatrix metalloproteinasesmedicine.anatomical_structureAdenocarcinomabusinessResearch ArticleBMC Clinical Pathology
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Isolation and Characterization of an Fe(III)-Chelating Compound Produced by Pseudomonas syringae

1986

The phytopathogenic bacterium Pseudomonas syringae produces a fluorescent pigment when it is grown in iron-deficient media. This pigment forms a very stable Fe(III) complex that was purified in this form by using a novel procedure based on ultrafiltration and column chromatography. The Fe(III) complex has a molecular weight of 1,100 and contains 1 mol of Fe(III). The pigment is composed of an amino acid moiety with three threonines, three serines, one lysine, δ- N -hydroxyornithine, and a quinoline-type fluorescent chromophore. These features and its stability constant (in the range of 10 32 ) suggest that the fluorescent pigment of P. syringae is related to the siderophores produced by an…

SiderophoreEcologyStereochemistryBiologybiology.organism_classificationApplied Microbiology and BiotechnologyFluorescenceMicrobiologyPigmentColumn chromatographyvisual_artPseudomonadalesPseudomonas syringaevisual_art.visual_art_mediumMoietyChelationMicroorganism-Plant InteractionsFood ScienceBiotechnologyApplied and Environmental Microbiology
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