Search results for "CONSTANT"

showing 10 items of 1718 documents

Different genomic organization and expression of immunoglobulin light-chain isotypes in the rainbow trout.

2000

cDNA studies have distinguished two isotypes of the rainbow trout (Oncorhynchus mykiss) immunoglobulin (Ig) light chain (designated L1 and L2). This study characterized genomic clones of these isotypes. L1 genes are arranged in clusters with single copies of variable (V), joining (J), and constant (C) segments. The transcriptional orientation of the V genes is opposite to that of the J and C segments, indicating that the V genes must be rearranged by inversion. L2 is also organized in clusters, consisting of two or three V, one J, and one C exon, all in the same transcriptional orientation. L1 and L2 of rainbow trout are similar to the previously identified cod and catfish clusters. Repeat …

DNA ComplementaryTATA boxImmunologyMolecular Sequence DataImmunoglobulin Variable RegionGene ExpressionBiologyImmunoglobulin light chainComplementary DNASequence Homology Nucleic AcidGeneticsAnimalsAmino Acid SequenceRNA MessengerEnhancerPromoter Regions GeneticGeneGenomic organizationGeneticsBase SequenceSequence Homology Amino AcidMolecular biologyImmunoglobulin IsotypesRegulatory sequenceOncorhynchus mykissImmunoglobulin Joining RegionImmunoglobulin Light ChainsSequence motifImmunoglobulin Constant RegionsImmunogenetics
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Relaxation phenomena in mixed isomeric alcohols by Mandelstam-Brillouin scattering

1991

Mandelstam-Brillouin scattering data in mixed isomeric alcohols n-pentanol (nPe-OH) and 2-methyl-2-butanol (2Me-2BuOH) are presented. The hypersonic velocity and normalized absorption are measured as a function of the scattering angle, in the temperature range from - 15-degrees-C to + 45-degrees-C, and as a function of n-PeOH molar fraction going from the pure n-PeOH to the pure 2Me-2BuOH. The experimental results confirm the existence of a shear relaxation phenomenon in the GHz region, that has been previously detected in pure liquids. The temperature dependence of the relaxation time tau-s and of the shear modulus G-infinity evaluated within viscoelastic liquid models, support the existen…

DYNAMICS2-METHYL-2-BUTANOLBiophysicsThermodynamicsN-PENTANOLViscoelasticityShear modulusOpticsRAMAN-SPECTROSCOPYBrillouin scatteringTEMPERATURESSUPERCOOLED WATERPhysical and Theoretical ChemistryMolecular BiologyBulk modulusChemistrybusiness.industryScatteringRelaxation (NMR)STATIC DIELECTRIC-CONSTANTCondensed Matter PhysicsLIGHT-SCATTERINGShear (sheet metal)Shear flowbusinessBONDVISCOSITYMolecular Physics
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s-wave charmed baryon resonances from a coupled-channel approach with heavy quark symmetry

2009

We study charmed baryon resonances which are generated dynamically within a unitary meson-baryon coupled channel model that treats the heavy pseudoscalar and vector mesons on equal footing as required by heavy-quark symmetry. It is an extension of recent SU(4) models with t-channel vector meson exchanges to a SU(8) spin-flavor scheme, but differs considerably from the SU(4) approach in how the strong breaking of the flavor symmetry is implemented. Some of our dynamically generated states can be readily assigned to recently observed baryon resonances, while others do not have a straightforward identification and require the compilation of more data as well as an extension of the model to d-w…

DYNAMICSQuarkNuclear and High Energy PhysicsParticle physicsDECAY CONSTANTSField theory (Physics)MesonHigh Energy Physics::LatticeNuclear TheoryFOS: Physical sciencesCHIRAL PERTURBATION-THEORY01 natural sciencesPartícules (Física nuclear)High Energy Physics - Phenomenology (hep-ph)UNITARY APPROACHHadron spectroscopy0103 physical sciencesSCATTERINGSymmetry breakingNuclear Experiment010306 general physicsParticles (Nuclear physics)PhysicsCLEBSCH-GORDAN COEFFICIENTS010308 nuclear & particles physicsHigh Energy Physics::PhenomenologyTeoria de camps (Física)FísicaSymmetry (physics)BaryonPseudoscalarCharmed baryonsHigh Energy Physics - PhenomenologySTATESKAON-NUCLEON INTERACTIONSMESON-MESONHigh Energy Physics::ExperimentBETHE-SALPETER APPROACHPhysical Review D
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Limit on the production of a light vector gauge boson in $\phi $ mesondecays with the KLOE detector

2012

We present a new limit on the production of a light dark-force mediator with the KLOE detector at DAPHNE. This boson, called U, has been searched for in the decay phi --> eta U, U --> e+ e-, analyzing the decay eta --> pi0 pi0 pi0 in a data sample of 1.7 fb-1. No structures are observed in the e+e- invariant mass distribution over the background. This search is combined with a previous result obtained from the decay eta --> pi+ pi- pi0, increasing the sensitivity. We set an upper limit at 90% C.L. on the ratio between the U boson coupling constant and the fine structure constant of alpha'/alpha < 1.7x10^-5 for 30<M_U<400 MeV and alpha'/alpha < 8x10^-6 for the sub-region 50<M_U<210 MeV. This…

Dark forcesNuclear and High Energy PhysicsParticle physicsElectron–positron annihilationFOS: Physical sciences01 natural sciencesSettore FIS/04 - Fisica Nucleare e Subnuclearee(+)e(-) Collisions Dark forces Gauge vector bosonHigh Energy Physics - ExperimentNuclear physicsHigh Energy Physics - Experiment (hep-ex)e(+)e(-) Collisions0103 physical sciencesgauge vector bosonInvariant massNuclear Experiment010306 general physicsBosonPhysicsCoupling constantGauge boson$e^{+}e^{-}$ collisions010308 nuclear & particles physicsSettore FIS/01 - Fisica SperimentaleForm factor (quantum field theory)Vector meson dominancePhi mesondark forcesHigh Energy Physics::ExperimentGauge vector boson
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Effective pseudopotential for energy density functionals with higher-order derivatives

2011

We derive a zero-range pseudopotential that includes all possible terms up to sixth order in derivatives. Within the Hartree-Fock approximation, it gives the average energy that corresponds to a quasi-local nuclear Energy Density Functional (EDF) built of derivatives of the one-body density matrix up to sixth order. The direct reference of the EDF to the pseudopotential acts as a constraint that divides the number of independent coupling constants of the EDF by two. This allows, e.g., for expressing the isovector part of the functional in terms of the isoscalar part, or vice versa. We also derive the analogous set of constraints for the coupling constants of the EDF that is restricted by sp…

Density matrixCoupling constantPhysicsNuclear and High Energy PhysicsNuclear Theoryta114IsovectorIsoscalarNuclear TheoryHartree–Fock methodFOS: Physical sciencesNuclear Theory (nucl-th)Constraint (information theory)PseudopotentialQuantum mechanicsHomogeneous spaceComputer Science::Operating SystemsPhysical Review C
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Solution and solid state studies with the bis-oxalato building block [Cr(pyim)(C2O4)2]− [pyim = 2-(2′-pyridyl)imidazole]

2013

The preparation, X-ray structure, and variable temperature magnetic study of the new compound {Ba(H2O)3/2[Cr(pyim)(C2O4)2]2}n·9/2nH2O (1) [pyim = 2-(2′-pyridyl)imidazole and C2O42− = dianion of oxalic acid], together with the potentiometric and spectrophotometric studies of the protonation/deprotonation equilibria of the pyim ligand and the ternary complex [Cr(pyim)(C2O4)2]−, are reported herein. The crystal structure of 1 consists of neutral chains, with diamond-shaped units sharing barium(II), with the two other corners occupied by chromium(III). The two metal centers are connected through bis(bidentate) oxalate. Very weak antiferromagnetic interactions between the chromium(III) ions occu…

DenticityInorganic chemistrychemistry.chemical_elementProtonationCrystal structureOxalateAcid dissociation constantchemistry.chemical_compoundChromiumCrystallographyDeprotonationchemistryMaterials ChemistryImidazolePhysical and Theoretical ChemistryJournal of Coordination Chemistry
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DNA-binding of nickel(II), copper(II) and zinc(II) complexes: structure-affinity relationships

2013

Abstract Nickel(II), copper(II) and zinc(II) complexes with the same ligands normally display analogous coordination geometry and binding mode toward DNA. However, although qualitatively alike in structure and properties, different DNA-binding ability has often been observed. This review surveys the most recent examples of binding of the three metal ions complexed with monodentate and chelating bidentate to tetradentate ligands to DNA. An attempt has also been made to rationalize the observed trend in the values of the intrinsic DNA-binding constant, Kb, in terms of structural and chemical features.

DenticityMetal ions in aqueous solutionInorganic chemistryBinding constantchemistry.chemical_elementZincDNABinding constantCopperSettore CHIM/08 - Chimica FarmaceuticaInorganic ChemistryNickelCrystallographyZincchemistryNickelSettore CHIM/03 - Chimica Generale E InorganicaMaterials ChemistryChelationPhysical and Theoretical ChemistryCopperCoordination geometry
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Effects of preorganization in the chelation of UO22+ by hydroxamate ligands: cyclic PIPO– vs linear NMA–

2018

International audience; Many siderophores incorporate as bidentate chelating subunits linear and more seldomly cyclic hydroxamate groups. In this work, a comparative study of the uranyl binding properties in aqueous solution of two monohydroxamic acids, the prototypical linear N-methylacetohydroxamic acid (NMAH) and the cyclic analog 1-hydroxypiperidine-2-one (PIPOH), has been carried out. The complex [UO2(PIPO)(2)(H2O)] crystallized from slightly acidic water solutions (pH < 5), and its molecular structure was determined by X-ray diffraction. The uranyl speciation in the presence of both ligands has been thoroughly investigated in a 0.1 M KNO3 medium at 298.2 K by the combined use of four …

DenticitySpeciation010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesCatalysisMetalchemistry.chemical_compounduranylMaterials Chemistry[CHIM.CRIS]Chemical Sciences/CristallographyMoleculeChelation[CHIM.COOR]Chemical Sciences/Coordination chemistry[PHYS]Physics [physics]Aqueous solutionLigandChemistryN-methylacetohydroxamic acidGeneral ChemistryUranyl0104 chemical sciencesCrystallographyStability constants of complexesvisual_artSolution thermodynamicscyclic hydroxamic acidvisual_art.visual_art_medium[CHIM.RADIO]Chemical Sciences/Radiochemistry
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The natural compound chrysosplenol-D is a novel, ultrasensitive optical sensor for detection of Cu(II)

2020

Abstract Herein, we introduce a novel, ultrasensitive optical sensor for determination of Cu(II) ions over the concentration range of 0 to 1 μM Cu(II). The optical sensor is based on the natural molecule chrysosplenol-D (Chp-D) extracted from the flowering plant Chiliadenus montanus (Vahl.) Brullo. Free Chp-D emits fluorescence at 566 nm when excited at 292 nm. Chp-D chelates Cu(II) ions to form a 1:1 (metal:ligand) complex, which quenches the fluorescence emission peak of the free probe at 566 nm. “Turn-off” luminescence could be easily determined and provided distinct proof of the chelation of Cu(II) ions by Chp-D. This novel optical sensor offers a considerable fluorescence mechanism (ch…

Detection limitChemistryAnalytical chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsCharge-transfer complex01 natural sciencesFluorescenceBinding constantAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materialssymbols.namesakeLinear rangeStokes shiftMaterials ChemistrysymbolsMoleculePhysical and Theoretical Chemistry0210 nano-technologyLuminescenceSpectroscopyJournal of Molecular Liquids
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eta1-Allypalladium complexes with tridentate PNP’ ligand for the assembly of modified Screen Printed Electrodes: an electrochemical study.

2015

Specific Pd-based organometallic complex, in particular the [Pd(η1-CH2–CH=CH2)(P–N–P’)]BF4 was used for the assembly of chemically modified Screen Printed Electrodes (SPEs) and their electrochemical reactivity was also investigated. For this purpose potassium ferricyanide, hexaammineruthenium(III) chloride, sodium hexachloroiridate-(III) hydrate, ascorbic acid (AA), uric acid (UA), acetaminophen (Ac), guanine (G) and adenine (A) were used to study the electron-transfer processes, which occurred at modified SPEs, fabricated by using the [Pd(η1-CH2–CH=CH2)(P–N–P’)]BF4, applying the drop casting procedure. Interesting results were obtained in the case of the guanine (G) quantitative detection,…

Detection limitElectrocatalysis towards guanine/GP-N-P complexesGuanineAnalytical chemistryPd center dot P-N-P complexesElectrochemistryAscorbic acidHeterogeneous electron-transfer kinetic constantsAnalytical Chemistry: Pdchemistry.chemical_compoundPotassium ferricyanidechemistrychemically modified SPEsElectrodeElectrochemistryReactivity (chemistry)Settore CHIM/01 - Chimica Analitica: Pd; P-N-P complexes; chemically modified SPEs; Electrochemistry; Heterogeneous electron-transfer kinetic constants electro-catalysis towards nucleic acidsHydrateNuclear chemistryelectro-catalysis towards nucleic acids
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