Search results for "oligonucleotide"

showing 10 items of 418 documents

Endoribonuclease IV. A poly(A)-specific ribonuclease from chick oviduct. 1. Purification of the enzyme.

1976

A new endoribonuclease, termed endoribonuclease IV, has been described. This enzyme has been isolated from chick oviducts and purified 15 000-fold in a 25% yield nearly to homogeneity. The nuclease, which specifically degrades poly(A), forms oligonucleotides of an average chain length of 10. These (A)-10 fragments are terminated by 3'-hydroxyl and 5'-phosphate groups. The enzyme has a pH optimum at 8.7, requires Mn2+ or Mg2+ as a cofactor, and has a molecular weight of about 45 000.

EndoribonucleaseOviductsBiologyBiochemistryCofactorStructure-Activity RelationshipRibonucleasesAnimalsMagnesiumchemistry.chemical_classificationNucleaseManganeseOligoribonucleotidesOligonucleotideEndoribonuclease IVEndonucleasesMolecular biologyEnzyme ActivationMolecular WeightKineticsEnzymeBiochemistrychemistryYield (chemistry)biology.proteinOviductFemalePoly AChickensEuropean journal of biochemistry
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Neutral deoxyribonucleases of HeLa S3 cells: electrophoretic separation, characterization, substrate specificity and mode of action.

1980

Extracts of HeLa S3 cells were electrophoresed on polyacrylamide gels; gel slices were eluted and the eluates were assayed for DNase activities against native and denatured DNA substrates in the presence of MgCl2 or Na2EDTA. Aliquots of each eluate were also assayed for their ability to nick the circular supercoiled PM2 phage DNA to distinguish endonucleases from exonucleases. Peaks of endonuclease activities were characterized as forming 3′-phospho-oligonucleotides or 5′-phospho-oligonucleotides by the use of oligonucleotides produced by these enzymes as substrates for the 5′-phosphate-specific snake venom exonuclease. The total activity of DNases in gel eluates was much higher than that i…

ExonucleasePolyacrylamideDNA Single-StrandedBiochemistrySubstrate SpecificityEndonucleasechemistry.chemical_compoundHumansMagnesiumEdetic Acidchemistry.chemical_classificationChromatographyDeoxyribonucleasesbiologyOligonucleotideHydrogen-Ion ConcentrationElectrophoresisEnzymeBiochemistrychemistryDNA Viralbiology.proteinElectrophoresis Polyacrylamide GelDNA CircularDeoxyribonucleasesDNAHeLa CellsEuropean journal of biochemistry
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Configurable low-cost plotter device for fabrication of multi-color sub-cellular scale microarrays.

2014

We report on the construction and operation of a low-cost plotter for fabrication of microarrays for multiplexed single-cell analyses. The printing head consists of polymeric pyramidal pens mounted on a rotation stage installed on an aluminium frame. This construction enables printing of microarrays onto glass substrates mounted on a tilt stage, controlled by a Lab-View operated user interface. The plotter can be assembled by typical academic workshops from components of less than 15 000 Euro. The functionality of the instrument is demonstrated by printing DNA microarrays on the area of 0.5 squared centimeters using up to three different oligonucleotides. Typical feature sizes are 5 μm diam…

FabricationMaterials scienceScale (ratio)NanotechnologyMultiplexingBiomaterialsUser-Computer InterfacePlotterHumansGeneral Materials ScienceBiochipOligonucleotide Array Sequence AnalysisEGF ReceptorsEpidermal Growth FactorOligonucleotideDNA-directed protein immobilization EGF receptors device automation multiplexed patterns polymer pen lithographyGeneral ChemistryMicrofluidic Analytical TechniquesErbB ReceptorsTissue Array AnalysisCosts and Cost AnalysisMCF-7 CellsPrintingDNA microarraySingle-Cell AnalysisBiotechnologySmall (Weinheim an der Bergstrasse, Germany)
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Microarray mRNA expression analysis of Fanconi anemia fibroblasts.

2007

Fanconi anemia (FA) cells are generally hypersensitive to DNA cross-linking agents, implying that mutations in the different <i>FANC</i> genes cause a similar DNA repair defect(s). By using a customized cDNA microarray chip for DNA repair- and cell cycle-associated genes, we identified three genes, cathepsin B (<i>CTSB</i>), glutaredoxin (<i>GLRX</i>), and polo-like kinase 2 (<i>PLK2</i>), that were misregulated in untreated primary fibroblasts from three unrelated FA-D2 patients, compared to six controls. Quantitative real-time RT PCR was used to validate these results and to study possible molecular links between FA-D2 and other FA subtypes.…

Fanconi anemia complementation group CMicroarrayDNA RepairDNA repairMrna expressionBiologyProtein Serine-Threonine KinasesCathepsin Bchemistry.chemical_compoundCytogeneticsFanconi anemiahemic and lymphatic diseasesGeneticsmedicineHumansRNA MessengerMolecular BiologyGeneGenetics (clinical)GlutaredoxinsOligonucleotide Array Sequence AnalysisGeneticsReverse Transcriptase Polymerase Chain ReactionGene Expression ProfilingCell CycleFibroblastsmedicine.diseaseMolecular biologyFanconi AnemiachemistryCase-Control StudiesDNACytogenetic and genome research
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Beneficial Effect of Shikonin on Experimental Colitis Induced by Dextran Sulfate Sodium in Balb/C Mice

2012

[EN] The naphthoquinone shikonin, a major component of the root of Lithospermum erythrorhizon, now is studied as an anti-inflammatory agent in the treatment of ulcerative colitis (UC). Acute UC was induced in Balb/C mice by oral administration of 5% dextran sodium sulfate (DSS). The disease activity index was evaluated, and a histologic study was carried out. Orally administered shikonin reduces induced UC in a dose-dependent manner, preventing the shortening of the colorectum and decreasing weight loss by 5% while improving the appearance of feces and preventing bloody stools. The disease activity index score was much lower in shikonin-treated mice than in the colitic group, as well as the…

FarmacologiaArticle SubjectPolymorphonuclear leukocytesNF-KAPPA-BActivationIntestinal inflammationPharmacologyInflammatory bowel diseaseBALB/cchemistry.chemical_compoundExperimental Murine ColitisOral administrationWeight lossInflammatory-bowel-diseasemedicineAntisense oligonucleotideAcid-induced colitisbiologybusiness.industrylcsh:Other systems of medicineLithospermum erythrorhizonbiology.organism_classificationNFKB1medicine.diseaselcsh:RZ201-999Ulcerative colitisNaphthoquinoneComplementary and alternative medicinechemistryUlcerative-colitisImmunologyCytokinesmedicine.symptombusinessAntiinflamatorisResearch ArticleEvidence-Based Complementary and Alternative Medicine
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Foxp3 Silencing with Antisense Oligonucleotide Improves Immunogenicity of an Adjuvanted Recombinant Vaccine against Sporothrix schenckii

2021

Made available in DSpace on 2021-06-25T10:56:14Z (GMT). No. of bitstreams: 0 Previous issue date: 2021-04-01 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Background: In recent years, there has been great interest in developing molecular adjuvants based on antisense oligonucleotides (ASOs) targeting immunosuppressor pathways with inhibitory effects on regulatory T cells (Tregs) to improve immunogenicity and vaccine efficacy. We aim to evaluate the immunostimulating effect of 2′OMe phosphorothioated Foxp3-targeted ASO in an antifungal adjuvanted recombinant vaccine. Methods: The uptake kinetics of Foxp3 ASO, its cyto-toxicity and its ability to deplete Tregs were evaluated in…

Farmacologiamedicine.medical_treatmentÀcids nucleicschemical and pharmacologic phenomenaCatalysisregulatory T cellslaw.inventionInorganic Chemistrylcsh:Chemistryvaccine immunogenicityImmune systemlawantisensense oligonucleotidemedicineVacunacióPhysical and Theoretical ChemistryMolecular Biologylcsh:QH301-705.5SpectroscopySporothrix schenckiibiologybusiness.industryImmunogenicityOrganic ChemistryAntibody titerGeneral MedicineFongs patògensVaccine efficacyComputer Science ApplicationsVaccinationlcsh:Biology (General)lcsh:QD1-999Foxp3ImmunologyRecombinant DNAbiology.proteinAntibody<i>Sporothrix schenckii</i>businessAdjuvantInternational Journal of Molecular Sciences
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Use of functional genes to quantify denitrifiers in the environment.

2006

During the last decade, application of molecular methods using cultivation-independent approaches has provided new insights into the composition and structure of denitrifying communities in various environments. However, little is known about their abundance, and quantification is still performed using cultivation-based approaches, which are not only biased by the inability to cultivate of many micro-organisms but also fastidious and time-consuming. Two types of cultivation-independent approaches have recently been developed to quantify denitrifiers. The first type, which is based on the hybridization technique, comprises the use of Southern hybridization and DNA arrays. The second type, ba…

Fastidious organismNitratesEcologyNucleic Acid HybridizationFunctional genesComputational biologyBiologyEnvironmentBiochemistryPolymerase Chain ReactionCompetitive pcrlaw.inventionlawMost probable numberGenes BacterialPolymerase chain reactionNitritesSoil MicrobiologySouthern blotOligonucleotide Array Sequence AnalysisBiochemical Society transactions
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A multi-layer method to study genome-scale positions of nucleosomes

2009

AbstractThe basic unit of eukaryotic chromatin is the nucleosome, consisting of about 150 bp of DNA wrapped around a protein core made of histone proteins. Nucleosomes position is modulated in vivo to regulate fundamental nuclear processes. To measure nucleosome positions on a genomic scale both theoretical and experimental approaches have been recently reported. We have developed a new method, Multi-Layer Model (MLM), for the analysis of nucleosome position data obtained with microarray-based approach. The MLM is a feature extraction method in which the input data is processed by a classifier to distinguish between several kinds of patterns. We applied our method to simulated-synthetic and…

Feature extractionNucleosome positioningGenomicsSaccharomyces cerevisiaeComputational biologyHidden Markov Modelchemistry.chemical_compoundSettore BIO/10 - BiochimicaNucleosome positioning Hidden Markov Model Classification Multi-layer methodGeneticsHumansNucleosomeMulti-layer methodHidden Markov modelBase PairingMulti layerOligonucleotide Array Sequence AnalysisGeneticsBase SequenceSettore INF/01 - InformaticabiologyGenome HumanClassificationMarkov ChainsNucleosomesChromatinHistonechemistrybiology.proteinDNAGenomics
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Pathogenetic and diagnostic significance of microRNA deregulation in peripheral T-cell lymphoma not otherwise specified

2014

Peripheral T-cell lymphomas not otherwise specified (PTCLs/NOS) are rare and aggressive tumours whose molecular pathogenesis and diagnosis are still challenging. The microRNA (miRNA) profile of 23 PTCLs/NOS was generated and compared with that of normal T-lymphocytes (CD4+, CD8+, naive, activated). The differentially expressed miRNA signature was compared with the gene expression profile (GEP) of the same neoplasms. The obtained gene patterns were tested in an independent cohort of PTCLs/NOS. The miRNA profile of PTCLs/NOS then was compared with that of 10 angioimmunoblastic T-cell lymphomas (AITLs), 6 anaplastic large-cell lymphomas (ALCLs)/ALK+ and 6 ALCLs/ALK - . Differentially expressed…

Female; Gene Expression Profiling; Humans; Lymphoma T-Cell Peripheral; Male; MicroRNAs; Oligonucleotide Array Sequence Analysis; RNA Neoplasm; Gene Expression Regulation Neoplastic; Oncology; Hematology; Medicine (all)Malemedicine.medical_specialtyPathologyPeripheral T-cell lymphoma not otherwise specifiedBiologyhemic and lymphatic diseasesInternal medicinemicroRNAmedicineHumansRNA NeoplasmOligonucleotide Array Sequence AnalysisRegulation of gene expressionHematologymicroRNA; PTCLs/NOS; GEPOligonucleotide Array Sequence AnalysiGene Expression ProfilingMedicine (all)Not Otherwise SpecifiedLymphoma T-Cell PeripheralMicroRNAHematologymedicine.diseaseGEPLymphomaGene expression profilingGene Expression Regulation NeoplasticMicroRNAsOncologyPTCLs/NOSOriginal ArticleFemaleCD8Human
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Paradigm of tunable clustering using Binarization of Consensus Partition Matrices (Bi-CoPaM) for gene discovery

2013

Copyright @ 2013 Abu-Jamous et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Clustering analysis has a growing role in the study of co-expressed genes for gene discovery. Conventional binary and fuzzy clustering do not embrace the biological reality that some genes may be irrelevant for a problem and not be assigned to a cluster, while other genes may participate in several biological functions and should simultaneously belong to multiple clusters. Also, these algorithms cannot generate tight cluster…

Fuzzy clusteringMicroarraysSingle-linkage clusteringGenes FungalGene Expressionlcsh:MedicineBiologyFuzzy logicSet (abstract data type)Molecular GeneticsEngineeringGenome Analysis ToolsYeastsConsensus clusteringMolecular Cell BiologyDatabases GeneticCluster (physics)GeneticsCluster AnalysisBinarization of Consensus Partition Matrices (Bi-CoPaM)Cluster analysislcsh:ScienceGene clusteringBiologyOligonucleotide Array Sequence AnalysisGeneticsMultidisciplinarybusiness.industryCell Cycleta111lcsh:RComputational BiologyPattern recognitionGenomicsgene discoveryPartition (database)tunable binarization techniquesComputingMethodologies_PATTERNRECOGNITIONGenesCell cyclesSignal Processinglcsh:QArtificial intelligencebusinessGenomic Signal ProcessingAlgorithmsResearch Articleclustering
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