Search results for "Assay"

showing 10 items of 2241 documents

Erratum to “Hydrolytic enzyme activity of Paenibacillus sp. strain B2 and effects of the antagonistic bacterium on cell integrity of two soil-borne p…

2001

Ce texte contient des corrections apportées à l'article " Hydrolytic enzyme activity of Paenibacillus sp. strain B2 and effects of the antagonistic bacterium on cell integrity of two soil-borne pathogenic fungi" sorti dans le numéro 15 du journal "Applied Soil Ecology" sorti en 2000.

EcologyStrain (chemistry)Soil ScienceBiologybiology.organism_classificationAgricultural and Biological Sciences (miscellaneous)Enzyme assayMicrobiologyHydrolysisSoil borneBotanyCell integritybiology.proteinPaenibacillus sp.Bacteria
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Development of a TaqMan PCR assay for the identification of the non-native copepod Acartia tonsa, and detection of this species in Norwegian coastal …

2021

Abstract Molecular based assays for detection of species are a powerful tool to supplement morphological methods that may be time and labor intensive. Here we describe a sensitive TaqMan real time polymerase chain reaction assay that specifically detects the presence of Acartia tonsa in mixed plankton samples. The assay is used to find this non-native copepod in samples collected in Norwegian coastal waters.

Ecologybiologyved/biologyfungiPcr assayved/biology.organism_classification_rank.speciesZoologyAquatic Sciencebiology.organism_classificationTaqManIdentification (biology)Ecology Evolution Behavior and SystematicsCopepodAcartia tonsaJournal of Plankton Research
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Reciprocal regulation of the human sterol regulatory element binding protein (SREBP)-1a promoter by Sp1 and EGR-1 transcription factors.

2007

AbstractSterol regulatory element binding protein (SREBP)-1a is a transcription factor that is highly expressed in actively growing cells, and is involved in the biosynthesis of cholesterol, fatty acids and phospholipids. We have mapped the minimal human SREBP-1a promoter region to 75bp upstream of the translation start site where we discovered a functional role for the 3 GC-boxes containing overlapping sites for the Sp1 and EGR-1 transcription factors. Intact SP1-binding sites are essential for promoter activity, whereas EGR-1 suppresses the transcription of the human SREBP-1a promoter. These results reveal a novel physiologically relevant transcriptional mechanism for the reciprocal regul…

Egr-1Chromatin ImmunoprecipitationSp1 Transcription FactorSREBP-1aResponse elementMolecular Sequence DataBiophysicsElectrophoretic Mobility Shift AssayBiologyBiochemistrySp1Cell LineUpstream activating sequenceStructural BiologyTranscription (biology)Sequence Homology Nucleic AcidGene expressionGeneticsHumansPromoter Regions GeneticMolecular BiologyTranscription factorGeneral transcription factorBase SequenceReverse Transcriptase Polymerase Chain ReactionPromoterPromoterCell BiologySterol regulatory element-binding proteinBiochemistryEarly Growth Response Transcription Factorslipids (amino acids peptides and proteins)Gene expressionSterol Regulatory Element Binding Protein 1FEBS letters
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Acute toxicity tests using earthworms to estimate ecological quality of compost and digestate

2017

Ecological quality of compost and digestate, used as fertilizers for agricultural use, was assessed through an acute ecotoxicological bioassay testing the earthworm Eisenia fetida (Annelida). The test evaluates the earthworm’s attitude to dig within 15 min into a soil medium constituted by a mixture of a standardized soil and different concentrations of compost/digestate. According to different classes of behavior responses, the sample is classified as good or bad quality (ON/OFF). The validity of this test was confirmed comparing the observations with the results from a standard chronic test developed by OECD (Organisation for Economic Co-operation and Development). Considering samples fro…

Eisenia fetida020209 energySoil biologyEcotoxicity testsSettore BIO/05 - ZoologiaDigestate02 engineering and technology010501 environmental sciencesengineering.material01 natural sciencesFertilizer0202 electrical engineering electronic engineering information engineeringBioassayWormsAgriculture application; Compost; Digestate; Ecotoxicity tests; Fertilizer; Worms; Waste Management and Disposal; Mechanics of MaterialsWaste Management and Disposal0105 earth and related environmental sciencesDigestate Compost Ecotoxicity tests Worms Fertilizer Agriculture applicationSettore ICAR/03 - Ingegneria Sanitaria-AmbientalebiologyCompostEcologybusiness.industryEarthwormAgriculture applicationCompostbiology.organism_classificationSettore AGR/11 - Entomologia Generale E ApplicataMechanics of MaterialsDigestateengineeringEnvironmental scienceFertilizerbusinessQuality assuranceAgriculture application; Compost; Digestate; Ecotoxicity tests; Fertilizer; Worms
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Detection of primary DNA damage in Chlamydomonas reinhardtii by means of modified microgel electrophoresis.

1997

The assessment of genotoxic potential in surface water requires test methods, among which are those that detect initial DNA damage in organisms of aquatic biocenosis. The microgel electrophoresis (MGE) "comet assay" was applied to a ubiquitous unicellular green alga (Chlamydomonas reinhardtii) to detect DNA damage caused by genotoxins. For this, the test protocol described by Singh NP et al. [Exp Cell Res 175: 184-191, 1988] was modified. Major modifications were the use of alkaline lysis buffer with ionic detergents and the reduction of preincubation and electrophoresis times. Short-time exposure of Chlamydomonas to the well-known genotoxicants 4-nitroquinoline-1-oxide (4-NQO), N-nitrosodi…

ElectrophoresisEpidemiologyDNA damageHealth Toxicology and MutagenesisChlamydomonas reinhardtiiBiologymedicine.disease_causeDimethylnitrosaminechemistry.chemical_compoundBotanymedicineAnimalsGenetics (clinical)Cell NucleusChlamydomonasDNAHydrogen PeroxideDNA Protozoanbiology.organism_classification4-Nitroquinoline-1-oxideComet assaychemistryBiophysicsDNA fragmentationAlkaline lysisGenotoxicityDNAChlamydomonas reinhardtiiWater Pollutants ChemicalDNA DamageEnvironmental and molecular mutagenesis
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A comparative investigation of DNA adducts, DNA strand breaks and gene mutations induced by benzo[a]pyrene and (+/-)-anti-benzo[a]pyrene-7,8-diol 9,1…

1997

Abstract Genotoxic effects of benzo[ a ]pyrene (BP) and its reactive metabolites (±)- anti -benzo[ a ]pyrene-7,8-diol 9,10-oxide ((±)- anti -BPDE) were comparatively investigated in vitro with the permanent human fibroblast cell line MRC5CV1. Induced DNA adducts were measured by 32 P-postlabeling, DNA strand breakage was determined by the comet assay and the HPRT gene mutation test was used to detect cytotoxicity and mutagenicity. Treatment of MRC5CV1 cells with S9 mix-activated BP or with (±)- anti -BPDE resulted in a concentration-dependent increase in DNA adducts and strand breaks. Genotoxic effects of BP and (±)- anti- BPDE were detected by 32 P-postlabeling and the comet assay with sim…

ElectrophoresisHypoxanthine PhosphoribosyltransferaseHealth Toxicology and Mutagenesis78-Dihydro-78-dihydroxybenzo(a)pyrene 910-oxideGene mutationmedicine.disease_causechemistry.chemical_compoundDNA AdductsDNA adductpolycyclic compoundsGeneticsmedicineBenzo(a)pyreneHumansGeneCells CulturedMutationChemistryMutagenicity TestsDNAFibroblastsMolecular biologyComet assayBenzo(a)pyreneBiochemistryGenetic TechniquesCell cultureMutationPhosphorus RadioisotopesDNADNA DamageMutagensMutation research
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Sea urchin embryos as an in vivo model for the assessment of manganese toxicity: developmental and stress response effects.

2009

In the marine environment increasing concentrations of bio-available compounds often result from anthropogenic activities. Among metal ions, manganese represents a new emergent factor in environmental contamination. Here, we studied the effects of manganese on Paracentrotus lividus sea urchin embryos using biological and biochemical approaches for the analysis of impact on development, tissue accumulation and stress markers. Embryos were continuously exposed from fertilization to manganese at concentrations ranging from 1.0 to 61.6 mg l(-1), monitored for developmental abnormalities at 48 h after fertilization, and used for atomic spectrometric analysis at various times from 6 to 72 h. We f…

Embryo NonmammalianHealth Toxicology and Mutagenesischemistry.chemical_elementApoptosisManganeseManagement Monitoring Policy and LawToxicologyParacentrotus lividusToxicologyHuman fertilizationStress PhysiologicalIn vivoToxicity TestsAnimalsManganeseTUNEL assaybiologyHSC70 Heat-Shock ProteinsEmbryoChaperonin 60General MedicineEmbryo-toxicity Marine environment Metal accumulation Stress proteins Apoptosis ROSbiology.organism_classificationCell biologychemistryModels AnimalToxicityParacentrotusBiomarkersWater Pollutants ChemicalIntracellular
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Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia

2020

Introduction Esophageal atresia with or without tracheoesophageal fistula (EA/TEF) occurs approximately 1 in 3.500 live births representing the most common malformation of the upper digestive tract. Only half a century ago, EA/TEF was fatal among affected newborns suggesting that the steady birth prevalence might in parts be due to mutational de novo events in genes involved in foregut development. Methods To identify mutational de novo events in EA/TEF patients, we surveyed the exome of 30 case-parent trios. Identified and confirmed de novo variants were prioritized using in silico prediction tools. To investigate the embryonic role of genes harboring prioritized de novo variants we perfor…

EmbryologyCandidate geneGene ExpressionTranscriptomeMiceDatabase and Informatics MethodsMedicine and Health SciencesExomeExomeExome sequencingGenetics0303 health sciencesMultidisciplinaryComputer-Aided Drug DesignQ030305 genetics & hereditySequence analysisRGenomicsCongenital AnomaliesDNA-Binding Proteinsembryonic structuresAmino Acid AnalysisMedicineTranscriptome AnalysisTracheoesophageal FistulaResearch ArticleDrug Research and DevelopmentBioinformaticsSequence analysisScienceIn silicoBiologyResearch and Analysis Methods03 medical and health sciencesExome SequencingGeneticsCongenital DisordersAnimalsHumansddc:610Molecular Biology TechniquesEsophageal AtresiaMolecular BiologyDNA sequence analysis030304 developmental biologyHomeodomain ProteinsPharmacologyMolecular Biology Assays and Analysis TechniquesGene Expression ProfilingEmbryosDNA HelicasesBiology and Life SciencesComputational BiologyEmbryo MammalianGenome AnalysisFANCBRepressor ProteinsGene expression profilingBiological DatabasesDrug DesignMutation DatabasesMutationDevelopmental Biology
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Dorsal root ganglia neurite outgrowth measured as a function of changes in microelectrode array resistance

2017

Current research in prosthetic device design aims to mimic natural movements using a feedback system that connects to the patient's own nerves to control the device. The first step in using neurons to control motion is to make and maintain contact between neurons and the feedback sensors. Therefore, the goal of this project was to determine if changes in electrode resistance could be detected when a neuron extended a neurite to contact a sensor. Dorsal root ganglia (DRG) were harvested from chick embryos and cultured on a collagen-coated carbon nanotube microelectrode array for two days. The DRG were seeded along one side of the array so the processes extended across the array, contacting a…

EmbryologyDistribution CurvesCell Culture Techniqueslcsh:MedicineElectrode Recording02 engineering and technologyChick Embryolaw.invention0302 clinical medicinelawAnimal CellsGanglia SpinalMedicine and Health SciencesElectric Impedancelcsh:ScienceMembrane ElectrophysiologyCells CulturedNeuronsProstheticsMultidisciplinaryChemistryMultielectrode arraymedicine.anatomical_structureBioassays and Physiological AnalysisElectrodePhysical SciencesEngineering and TechnologyCellular TypesResearch ArticleStatistical DistributionsBiotechnologyDorsumNeuritePhase contrast microscopy0206 medical engineeringNeuronal OutgrowthResearch and Analysis Methods03 medical and health sciencesmedicineNeuritesAnimalsElectrodeslcsh:RElectrophysiological TechniquesEmbryosBiology and Life SciencesCell BiologyNeuronal DendritesChick embryosProbability Theory020601 biomedical engineeringAssistive Technologiesnervous systemReference ElectrodesCellular Neurosciencelcsh:QMedical Devices and EquipmentNeuronElectronicsMicroelectrodes030217 neurology & neurosurgeryMathematicsBiomedical engineeringNeuroscienceDevelopmental BiologyPLoS ONE
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T helper 17 lineage differentiation is programmed by orphan nuclear receptors ROR alpha and ROR gamma.

2007

T cell functional differentiation is mediated by lineage-specific transcription factors. T helper 17 (Th17) has been recently identified as a distinct Th lineage mediating tissue inflammation. Retinoic acid receptor-related orphan receptor gamma (ROR gamma) was shown to regulate Th17 differentiation; ROR gamma deficiency, however, did not completely abolish Th17 cytokine expression. Here, we report Th17 cells highly expressed another related nuclear receptor, ROR alpha, induced by transforming growth factor-beta and interleukin-6 (IL-6), which is dependent on signal transducer and activator of transcription 3. Overexpression of ROR alpha promoted Th17 differentiation, possibly through the c…

Encephalomyelitis Autoimmune ExperimentalReceptors Retinoic AcidT cellImmunologyRetinoic acidReceptors Cytoplasmic and NuclearElectrophoretic Mobility Shift AssayBiology03 medical and health scienceschemistry.chemical_compoundMice0302 clinical medicineT-Lymphocyte SubsetsmedicineT helper 17 cellImmunology and AllergyAnimalsCell LineageReceptorMOLIMMUNOTranscription factor030304 developmental biologyOrphan receptor0303 health sciencesReceptors Thyroid HormoneReverse Transcriptase Polymerase Chain ReactionInterleukin-17Cell DifferentiationNuclear Receptor Subfamily 1 Group F Member 1T-Lymphocytes Helper-InducerNuclear Receptor Subfamily 1 Group F Member 3Molecular biologyMice Mutant StrainsCell biologymedicine.anatomical_structureInfectious DiseaseschemistryNuclear receptorSTAT proteinTrans-ActivatorsFemale030215 immunologyImmunity
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