Search results for "AMPLIFICATION"

showing 10 items of 258 documents

Ytterbium-doped fibers for high-power fiber lasers

2021

Ytterbium (Yb) doped optical fibers are widely used in high-power applications and ultrafast lasing since they show adequate power-handling capability and provide desirable beam quality. Yb-doped fibers with large core area can support high power but often act as a multimode fiber and compromise the output beam quality. Hence, it is important to attain a proper balance between the power-handling capability and the beam quality. Yb-doped fibers as a gain medium in pulsed fiber laser systems are prone to nonlinear optical effects due to the presence of high peak power in the ultrashort pulses. Nonlinearity such as self phase modulation (SPM) affects the width and the shape of the pulse, both …

Chirped pulse amplificationoptiset kuidutOptical fiberMulti-mode optical fiberMaterials sciencebusiness.industrydouppaus (puolijohdetekniikka)Physics::Opticslasertekniikkalaw.inventionlaseritkuituoptiikkaOpticslawFiber laserChirpLaser beam qualitybusinessSelf-phase modulationUltrashort pulse
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Investigations for fine mapping of amplifications in chromosome 3q26.3-28 frequently occurring in squamous cell carcinomas of the head and neck.

2002

<i>Objective:</i> Overrepresentations of chromosomal material on the long arm of chromosome 3 frequently occur in squamous cell carcinoma of the head and neck. This experimental study was conducted for further fine mapping of these overrepresentations by interphase fluorescence in situ hybridization (FISH) of tumor cells in cell lines. <i>Methods:</i> Seven cell lines derived from squamous cell carcinomas of the head and neck were investigated by comparative genomic hybridization to analyze unbalanced chromosomal aberrations. Overrepresentations of chromosomal material on the telomeric part of the long arm of chromsome 3 were further analyzed by interphase FISH using…

Chromosome AberrationsCancer Researchmedicine.diagnostic_testCellGene AmplificationChromosomeChromosome MappingGeneral MedicineBiologyMolecular biologymedicine.anatomical_structureOncologyChromosome 3Cell cultureHead and Neck NeoplasmsmedicineCarcinoma Squamous CellTumor Cells CulturedHumansBasal cellChromosomes Human Pair 3Head and neckIn Situ Hybridization FluorescenceComparative genomic hybridizationFluorescence in situ hybridizationOncology
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A Novel Chitin-binding Protein from the Vestimentiferan Riftia pachyptila Interacts Specifically with β-Chitin

2001

Abstract A cDNA from Riftia pachyptila was cloned. It encodes a novel 21.3-kDa protein from the worm protective tube, named RCBP (for Riftia chitin-binding protein). On the basis of partial tube-peptide sequences previously obtained, experiments using reverse transcriptase-mediated polymerase chain reaction and rapid amplification of cDNA ends led to the complete cDNA sequence. Analysis of its deduced amino acid sequence shows the presence of two chitin-binding domains. These domains are closely related to type 2 chitin-binding domains that are restricted to the animal kingdom. We showed by affinity assay and immunogold labeling that RCBP is the first protein so far known that binds specifi…

CloningMessenger RNACell BiologyImmunogold labellingBiologyBiochemistryMolecular biologychemistry.chemical_compoundChitinchemistryRapid amplification of cDNA endsBiochemistryChitin bindingComplementary DNAMolecular BiologyPeptide sequenceJournal of Biological Chemistry
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Search by Quantum Walks on Two-Dimensional Grid without Amplitude Amplification

2013

We study search by quantum walk on a finite two dimensional grid. The algorithm of Ambainis, Kempe, Rivosh [AKR05] uses \(O(\sqrt{N \log{N}})\) steps and finds a marked location with probability O(1 / logN) for grid of size \(\sqrt{N} \times \sqrt{N}\). This probability is small, thus [AKR05] needs amplitude amplification to get Θ(1) probability. The amplitude amplification adds an additional \(O(\sqrt{\log{N}})\) factor to the number of steps, making it \(O(\sqrt{N} \log{N})\).

CombinatoricsDiscrete mathematicsAmplitude amplification010201 computation theory & mathematics0103 physical sciencesQuantum walk0102 computer and information sciencesNuclear Experiment010306 general physicsGrid01 natural sciencesMathematics
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Magnetic field amplification and magnetically supported explosions of collapsing, non-rotating stellar cores

2014

We study the amplification of magnetic fields in the collapse and the post-bounce evolution of the core of a non-rotating star of 15 solar masses in axisymmetry. To this end, we solve the coupled equations of magnetohydrodynamics and neutrino transport in the two-moment approximation. The pre-collapse magnetic field is strongly amplified by compression in the infall. Initial fields of the order of 1010 G translate into proto-neutron star fields similar to the ones observed in pulsars, while stronger initial fields yield magnetar-like final field strengths. After core bounce, the field is advected through the hydrodynamically unstable neutrino-heating layer, where non-radial flows due to con…

ConvectionPhysicsMagnetic energyAdvectionAstrophysics::High Energy Astrophysical PhenomenaFOS: Physical sciencesAstronomy and AstrophysicsMechanicsAstrophysicsAmplification factorInstabilityMagnetic fieldAstrophysics - Solar and Stellar AstrophysicsSpace and Planetary ScienceMagnetohydrodynamicsSolar and Stellar Astrophysics (astro-ph.SR)Equipartition theoremMonthly Notices of the Royal Astronomical Society
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Determination of DNA single strand breaks and selective DNA amplification by N-nitrodimethylamine and analogs, and estimation of the indicator cells'…

1986

N-nitrodimethylamine is metabolized oxidatively to N-nitrohydroxymethylmethylamine, which decomposes to yield formaldehyde and N-nitromethylamine. All four compounds and N-nitromethylamine were tested for their ability to induce DNA single strand breaks in hepatocytes and in SV 40-transformed Chinese hamster embryo cell lines. Only the two monoalkylnitramines were positive. They induced single strand breaks in hepatocytes, but were not effective in the other cells. Formaldehyde and N-nitrohydroxymethylmethylamine were toxic to the cells. None of the compounds tested was able to induce selective DNA amplification in the two transformed cell lines. Enzymes involved in drug metabolism were ass…

DNA ReplicationCancer ResearchHamsterDNA Single-StrandedSimian virus 40BiologyChinese hamsterCell Linechemistry.chemical_compoundCricetulusCricetinaeFormaldehydeAnimalsEpoxide hydrolaseCells Culturedchemistry.chemical_classificationDose-Response Relationship DrugDNA replicationGene AmplificationGeneral Medicinebiology.organism_classificationCell Transformation ViralEmbryo MammalianRatsEnzymeOncologychemistryBiochemistryLiverCell cultureDrug metabolismDNADimethylaminesJournal of cancer research and clinical oncology
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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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DNA Amplification Fingerprinting for Subtyping Neisseria gonorrhoeae Strains

1995

Background and Objectives DNA amplification fingerprinting is used in most epidemiologic studies as a substitute for conventional typing methods. DNA amplification fingerprinting and conventional typing methods were compared in this epidemiologic study of Neisseria gonorrhoeae. Goal of This Study To differentiate 70 Neisseria gonorrhoeae isolates from untreated patients with urogenital gonococcal infection. Study Design Gonococcal strains were characterized by auxo-typing, serotyping, plasmid profile, antibiotic sensitivity, and DNA amplification fingerprinting. The method of unweighted pair-group average linkage was used for cluster analysis. Discriminatory power was calculated applying Si…

DNA BacterialMicrobiology (medical)SerotypeSexually transmitted diseasePenicillin ResistanceMolecular Sequence DataMicrobial Sensitivity TestsDermatologyBiologymedicine.disease_causechemistry.chemical_compoundPlasmidmedicineHumansSerotypingElectrophoresis Agar GelGeneticsBase SequencePublic Health Environmental and Occupational HealthNucleic acid amplification techniquebiology.organism_classificationDNA FingerprintingVirologyNeisseria gonorrhoeaeSubtypingBacterial Typing TechniquesInfectious DiseaseschemistryNeisseria gonorrhoeaeNeisseriaceaeNucleic Acid Amplification TechniquesDNASexually Transmitted Diseases
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Use of nodulation pattern, stress tolerance, nodC gene amplification, RAPD-PCR and RFLP-16S rDNA analysis to discriminate genotypes of Rhizobium legu…

2005

Twenty-seven new Rhizobium isolates were obtained from root nodules of wild and crop legumes belonging to the genera Vicia, Lathyrus and Pisum from different agroecological areas in central and southern Italy. A polyphasic approach including phenotypic and genotypic techniques was used to study their diversity and their relationships with other biovars and species of rhizobia. Analysis of symbiotic properties and stress tolerance tests revealed that wild isolates, showed a wide spectrum of nodulation and a marked variation in stress tolerance compared with reference strains tested in this study. All rhizobial isolates (except for the isolate CG4 from Galega officinalis) were presumptively i…

DNA BacterialRoot noduleGenotypeStress toleranceBiologymedicine.disease_causeN-AcetylglucosaminyltransferasesApplied Microbiology and BiotechnologyMicrobiologyDNA RibosomalPolymerase Chain ReactionMediterranean areaRhizobium leguminosarumRhizobiaBacterial ProteinsRhizobium leguninosarumNodC geneStress toleranceWild legumesStrains diversityMediterranean areaSymbiotic characteristicsRNA Ribosomal 16SmedicineSymbiosisEcology Evolution Behavior and SystematicsGeneticsPrincipal Component AnalysisRhizobium leguminosarumfood and beveragesFabaceaeNucleic acid amplification techniqueNodC geneHydrogen-Ion ConcentrationRhizobium leguninosarum16S ribosomal RNAbiology.organism_classificationStrains diversitySymbiotic characteristicsRAPDBacterial Typing TechniquesRandom Amplified Polymorphic DNA TechniqueRhizobiumWild legumeRestriction fragment length polymorphismNucleic Acid Amplification TechniquesPolymorphism Restriction Fragment LengthSettore AGR/16 - Microbiologia Agraria
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Identification and typing of food-borne Staphylococcus aureus by PCR-based techniques.

2005

Abstract The possibility of using PCR for rapid identification of food-borne Staphylococcus aureus isolates was evaluated as an alternative to the API-Staph system. A total of 158 strains, 15 S. aureus , 12 other staphylococcal species, and 131 isolates recovered from 164 food samples were studied. They were phenotypically characterized by API-Staph profiles and tested for PCR amplification with specific primers directed to thermonuclease ( nuc ) and enterotoxin ( sea to see ) genes. Disagreement between the PCR results and API-Staph identification was further assessed by the analysis of randomly amplified polymorphic DNA (RAPD) profiles obtained with three universal primers (M13, T3, and T…

DNA BacterialStaphylococcus aureusMicrococcaceaeEnterotoxinBiologymedicine.disease_causeApplied Microbiology and BiotechnologyMicrobiologyDNA RibosomalPolymerase Chain Reactionlaw.inventionMicrobiologyEnterotoxinsfluids and secretionsBacterial ProteinslawRNA Ribosomal 16SGenotypemedicineCluster AnalysisMicrococcal NucleaseTypingEcology Evolution Behavior and SystematicsPolymerase chain reactionGenes rRNASequence Analysis DNAbiology.organism_classification16S ribosomal RNAEndonucleasesMolecular biologyDNA FingerprintingRAPDBacterial Typing TechniquesRandom Amplified Polymorphic DNA TechniqueStaphylococcus aureusFood MicrobiologyNucleic Acid Amplification TechniquesSystematic and applied microbiology
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