Search results for "Rapid"

showing 10 items of 1173 documents

Immunoanalytical approaches for the control of xenobiotics and biotoxins in food

2020

[ES] El control efectivo de la calidad y seguridad de los ali­mentos requiere de métodos analíticos que garanticen la deter­minación fiable de cualquier sustancia potencialmente perjudicial para el consumidor que pueda estar presente en el alimento antes de su distribución y comercialización. Una de las aproximaciones analíticas que contribuye a garantizar este objetivo engloba una serie de técnicas que tienen en común la utilización de anticuerpos como elementos esenciales para la detección del analito diana, y que en conjunto reciben el nombre de métodos inmunoquímicos. Este artículo pretender aportar una visión básica de los principios bioquímicos subyacentes a estas tecnologías y cuáles…

Cultural StudiesAnalyteAnticuerposSociology and Political ScienceComputer scienceContaminanteTira inmunorreactivarapid methods01 natural sciencesGeneral Works0404 agricultural biotechnologyantibodyresidueAChemical contaminantsimmunoassayMétodos rápidosGeneral Arts and Humanities010401 analytical chemistry04 agricultural and veterinary sciences040401 food sciencefood quality and safety0104 chemical sciencesanticuerpoimmunostriphaptenCalidad y seguridad de alimentosTechnology transferInmunoensayoELISAHaptenoBiochemical engineeringFood qualitycontaminantResiduo
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Measurement of dijet production with a veto on additional central jet activity in pp collisions at sqrt(s)=7 TeV using the ATLAS detector

2011

A measurement of jet activity in the rapidity interval bounded by a dijet system is presented. Events are vetoed if a jet with transverse momentum greater than 20 GeV is found between the two boundary jets. The fraction of dijet events that survive the jet veto is presented for boundary jets that are separated by up to six units of rapidity and with mean transverse momentum 50 < p¯T < 500 GeV. The mean multiplicity of jets above the veto scale in the rapidity interval bounded by the dijet system is also presented as an alternative method for quantifying perturbative QCD emission. The data are compared to a next-to-leading order plus parton shower prediction from the powheg-box, an all-order…

DIJETSParticle physicsNuclear and High Energy Physics:Mathematics and natural science: 400::Physics: 430 [VDP]Ciências Naturais::Ciências FísicasAtlas detectorAstrophysics::High Energy Astrophysical Phenomena:Ciências Físicas [Ciências Naturais]Monte Carlo methodFOS: Physical sciencesddc:500.2:Mathematics and natural science: 400::Physics: 430::Nuclear and elementary particle physics: 431 [VDP]01 natural sciences530High Energy Physics - ExperimentNuclear physicsHigh Energy Physics - Experiment (hep-ex)0103 physical sciences[PHYS.HEXP]Physics [physics]/High Energy Physics - Experiment [hep-ex]Rapidityddc:530High Energy PhysicsResummation010306 general physicsParton showerNuclear ExperimentPhysicsScience & TechnologyHadron-Hadron Scattering010308 nuclear & particles physicsSettore FIS/01 - Fisica SperimentaleHigh Energy Physics::PhenomenologyPerturbative QCDATLASBounded functionHADRON-HADRON COLLISIONSTransverse momentumFísica nuclearHigh Energy Physics::ExperimentLHCParticle Physics - Experiment
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Selective, Highly Sensitive, and Rapid Detection of Genomic DNA by Using Gated Materials:MycoplasmaDetection

2013

The coupling of gated-indicator delivery with highly specific biochemical recognition is an innovative strategy for the detection of DNA sequences, able to compete with classical methods which need PCR amplification, in important areas such as point-of-care diagnostics or detection of specific biological contaminations with pathogens. Such comparatively simple and cheap yet highly selective and sensitive assays hold promise for use in less-developed areas of the world.

DNA BacterialINGENIERIA DE LA CONSTRUCCIONSupportsMesoporous silica nanoparticlesFermentansResponsive controlled releaseAmplificationmesoporous materialsBiologysensorsmedicine.disease_causeRapid detectionCatalysisgated materialschemistry.chemical_compoundMycoplasmaQUIMICA ORGANICAContaminationQUIMICA ANALITICABIOQUIMICA Y BIOLOGIA MOLECULARmedicineGated materialsRheumatoid arthritismycoplasmaControlled drug deliverySensorsQUIMICA INORGANICAGenomicsDNAGeneral ChemistryMycoplasmaCell culturesMolecular biologyHighly sensitivegenomic DNAchemistryDNAAngewandte Chemie International Edition
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Characterization of a cDNA encoding RP43, a CUB-domain-containing protein from the tube of Riftia pachyptila (Vestimentifera), and distribution of it…

2000

A major 43kDa protein from the protective tube of Riftiapachyptila (Vestimentifera), named RP43, was partly microsequenced after isolation by SDS/PAGE from the protein fraction of tubes collected around the hydrothermal vents at the East Pacific Rise. On the basis of the partial peptide sequences obtained, experiments using reverse-transcriptase-mediated PCR and rapid amplification of cDNA ends led to the complete cDNA sequence. Analysis of deduced amino acid sequence of RP43 showed the presence of CUB domains (100–110-residue-spanning domains first reported in the complement subcomponents C1r/C1s, epidermal-growth-factor-related sea urchin protein and bone morphogenetic protein 1) that se…

DNA ComplementaryTranscription GeneticAnnelidaMolecular Sequence DataChitinPeptideBioinformaticsBiochemistryEpitheliumBone morphogenetic protein 1Rapid amplification of cDNA endsSequence Analysis ProteinComplementary DNAbiology.animalAnimalsAmino Acid SequenceRNA MessengerCloning MolecularMolecular BiologyPeptide sequenceSea urchinChromatography High Pressure LiquidIn Situ Hybridizationchemistry.chemical_classificationMessenger RNABase SequenceSequence Homology Amino AcidbiologyReverse Transcriptase Polymerase Chain ReactionHelminth ProteinsSequence Analysis DNACell BiologyBlotting NorthernCUB domainProtein Structure TertiaryCell biologychemistryElectrophoresis Polyacrylamide GelEpidermisProtein BindingResearch ArticleBiochemical Journal
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Molecular cloning of rat G-protein-coupled receptor kinase 6 (GRK6) from brain tissue, and its mRNA expression in different brain regions and periphe…

1997

The rat G-protein-coupled receptor kinase 6 (GRK6) cDNA was cloned from rat brain tissue by a combination of reverse-transcription polymerase chain reactions (RT-PCR), based on homology to the cloned human GRK6, and rapid amplification of cDNA ends (RACE-PCR). We obtained a clone of 2817 bp with an open reading frame of 1731 bp encoding for a protein of 576 amino acids that is 96.7% identical and 97.9% similar to its human counterpart. mRNA was detectable in all brain areas examined. In addition, GRK6 was expressed in skeletal muscle, small intestine, aorta, liver, heart, lung, thymus, stomach, uterus and kidney.

DNA ComplementaryTranscription GeneticMolecular Sequence DataProtein Serine-Threonine KinasesMolecular cloningBiologyPolymerase Chain ReactionOpen Reading FramesCellular and Molecular NeuroscienceRapid amplification of cDNA endsGTP-Binding ProteinsComplementary DNAGene expressionAnimalsHumansAmino Acid SequenceRNA MessengerCloning MolecularProtein kinase AMolecular BiologyG protein-coupled receptor kinaseMessenger RNABase SequenceSequence Homology Amino AcidBrainReceptor Protein-Tyrosine KinasesG-Protein-Coupled Receptor KinasesMolecular biologyRatsOpen reading frameOrgan SpecificityFemaleSequence AlignmentMolecular Brain Research
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Adequate Training and Multidisciplinary Support May Assist Pediatricians in Properly Handling and Managing Gender Incongruence and Dysphoria.

2022

What we call “sexual identity” refers to the complex relationship between biological sex, gender identity and role, and sexual orientation.1 “Gender identity” means the unified and persistent perception of oneself as belonging to the male or the female gender or ambivalent. For many, gender identity coincides with sexual identity; traditional culture has long provided for the definition of only 2 genders, corresponding to the 2 biological sexes. The person with gender incongruence experiences a disharmony between biological aspects and gender identity, with the constant awareness that he or she belongs to the opposite gender and is imprisoned in a body that does not represent him or her. Ge…

Depressive Disorder MajorPediatrics Perinatology and Child HealthHumansPediatriciansGender DysphoriaROGD (Rapid-onset of gender dysphoria)Transgender PersonsThe Journal of pediatrics
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"Table 2" of "Heavy flavour decay muon production at forward rapidity in proton--proton collisions at \sqrt(s) = 7 TeV"

2012

y-differential production cross section of muons from heavy flavour decays, in the range 2

Di-Muon ProductionPhysics::Instrumentation and DetectorsHigh Energy Physics::LatticeRapidity DependenceHigh Energy Physics::Phenomenology7000.0DSIG/DYRAPMuon productionInclusiveSingle Differential Cross SectionP P --&gt; CHARM CHARMBAR XProton-Proton ScatteringP P --&gt; BOTTOM BOTTOMBAR XPhysics::Accelerator PhysicsHigh Energy Physics::ExperimentP P --&gt; MU+ MU- X
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Induction of tcI 7 , a gene encoding a β-subunit of proteasome, in tobacco plants treated with elicitins, salicylic acid or hydrogen peroxide 1

2000

We previously isolated, by differential display and 5′ RACE (rapid amplification of cDNA ends), cDNAs corresponding to genes activated following cryptogein treatment of tobacco cell suspensions, among them tcI 7 (tcI for obacco ryptogein nduced), a gene encoding a β-subunit of proteasome. Here, we report that tcI 7 was up-regulated in tobacco plants treated with elicitins (cryptogein and parasiticein) that have been shown to induce a systemic acquired resistance (SAR). Moreover, subsequent inoculation of tobacco with the pathogen Phytophthora parasitica var. nicotianae (Ppn) was shown to induce an additional activation of tcI 7 in tobacco plants pretreated with cryptogein. We also showed an…

Differential displayfungiBiophysicsElicitinCell BiologyBiologyBiochemistryMolecular biologychemistry.chemical_compoundRapid amplification of cDNA endschemistryStructural BiologyRegulatory sequenceGene expressionGeneticsMYBMolecular BiologySalicylic acidSystemic acquired resistanceFEBS Letters
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Diffractive vector meson production in ultraperipheral heavy ion collisions from the Color Glass Condensate

2014

We compute cross sections for incoherent and coherent diffractive J/$\Psi$ and $\Psi(2S)$ production in ultraperipheral heavy ion collisions. The dipole models used in these calculations are obtained by fitting the HERA deep inelastic scattering data and compared with available electron-proton diffraction measurements. We obtain a reasonably good description of the available ALICE data. We find that the normalization of the ultraperipheral cross section has large model dependence, but the rapidity dependence is more tightly constrained.

DiffractionPhysicsNuclear TheoryFOS: Physical sciencesHERADeep inelastic scatteringColor-glass condensateNuclear physicsNuclear Theory (nucl-th)High Energy Physics - PhenomenologyCross section (physics)DipoleHigh Energy Physics - Phenomenology (hep-ph)High Energy Physics::ExperimentRapidityVector meson
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Hard single diffraction in p̄p collisions at s=630 and 1800 GeV

2002

Using the D empty set detector, we have studied events produced in (p) over barp collisions that contain large forward regions with very little energy deposition ("rapidity gaps") and concurrent jet production at center-of-mass energies of roots = 630 and 1800 GeV. The fraction of events with forward or central jets associated with rapidity gaps is compared to predictions for hard diffraction. We also extract the momentum loss for scattered protons in such processes. (C) 2002 Elsevier Science B.V. All rights reserved.

DiffractionPhysicsParticle physicsNuclear and High Energy Physics010308 nuclear & particles physicsDetectorEmpty setHERAJet (particle physics)01 natural sciencesNuclear physicsPomeron0103 physical sciencesMomentum lossRapidityHigh Energy Physics::Experiment010306 general physicsPhysics Letters B
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