Search results for "Microscopy"

showing 10 items of 3390 documents

TFIIH Operates through an Expanded Proximal Promoter To Fine-Tune c-myc Expression

2004

A continuous stream of activating and repressing signals is processed by the transcription complex paused at the promoter of the c-myc proto-oncogene. The general transcription factor IIH (TFIIH) is held at promoters prior to promoter escape and so is well situated to channel the input of activators and repressors to modulate c-myc expression. We have compared cells expressing only a mutated p89 (xeroderma pigmentosum complementation group B [XPB]), the largest TFIIH subunit, with the same cells functionally complemented with the wild-type protein (XPB/wt-p89). Here, we show structural, compositional, and functional differences in transcription complexes between XPB and XPB/wt-89 cells at t…

Chromatin ImmunoprecipitationDNA ComplementaryCell SurvivalUltraviolet RaysBlotting WesternGreen Fluorescent ProteinsGene ExpressionRepressorCellular homeostasisBiologyTransfectionModels BiologicalProto-Oncogene MasProto-Oncogene Proteins c-mycTranscription Factors TFIIRibonucleasesPotassium PermanganateTranscription (biology)HumansRNA MessengerPromoter Regions GeneticMolecular BiologyModels GeneticGeneral transcription factorCell CycleGenetic Complementation TestDNA HelicasesPromoterCell BiologyFibroblastsFlow CytometryMolecular biologyDNA-Binding ProteinsKineticsTranscription Factor TFIIHMicroscopy FluorescenceMutationTranscription preinitiation complexTranscription factor II HTranscription Factor TFIIHPlasmidsMolecular and Cellular Biology
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The Saccharomyces cerevisiae Hot1p regulated gene YHR087W (HGI1) has a role in translation upon high glucose concentration stress.

2012

Abstract Background While growing in natural environments yeasts can be affected by osmotic stress provoked by high glucose concentrations. The response to this adverse condition requires the HOG pathway and involves transcriptional and posttranscriptional mechanisms initiated by the phosphorylation of this protein, its translocation to the nucleus and activation of transcription factors. One of the genes induced to respond to this injury is YHR087W. It encodes for a protein structurally similar to the N-terminal region of human SBDS whose expression is also induced under other forms of stress and whose deletion determines growth defects at high glucose concentrations. Results In this work …

Chromatin ImmunoprecipitationTranslation<it>Saccharomyces cerevisiae</it>Saccharomyces cerevisiae Proteinslcsh:QH426-470Monosaccharide Transport ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiaeBiologyGene YHR087WHog1pTranscripció genèticaEukaryotic translationStress PhysiologicalPolysomeGene Expression Regulation FungalGene expressionProtein biosynthesisHigh glucose osmotic stresslcsh:QH573-671Transcription factorMolecular BiologyRegulation of gene expressionGenetic transcriptionlcsh:CytologyComputational BiologyTranslation (biology)biology.organism_classificationBlotting NorthernExpressió gènicaYeastlcsh:GeneticsGlucoseBiochemistryMicroscopy FluorescencePolyribosomesProtein BiosynthesisPolysomesGene <it>YHR087W</it>Gene expressionLlevatsMitogen-Activated Protein KinasesHot1pTranscription FactorsResearch ArticleBMC molecular biology
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Biogenic synthesis of palladium nanoparticles using Pulicaria glutinosa extract and their catalytic activity towards the Suzuki coupling reaction.

2014

Green synthesis of nanomaterials finds the edge over chemical methods due to its environmental compatibility. Herein, we report a facile and eco-friendly method for the synthesis of palladium (Pd) nanoparticles (NPs) using an aqueous solution of Pulicaria glutinosa, a plant widely found in a large region of Saudi Arabia, as a bioreductant. The as-prepared Pd NPs were characterized using ultraviolet-visible (UV-vis) spectroscopy, powder X-ray diffraction (XRD), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), and Fourier transform-infrared spectroscopy (FT-IR). The hydroxyl groups of the plant extract (PE) molecules were found mainly responsible for the red…

Chromatography GasMagnetic Resonance SpectroscopyStereochemistrychemistry.chemical_elementNanoparticleLigandsCatalysisCatalysisNanomaterialsPulicariaInorganic ChemistrySuzuki reactionMicroscopy Electron TransmissionX-Ray DiffractionSpectroscopy Fourier Transform InfraredMoleculeAqueous solutionChemistryPlant ExtractsX-RaysTemperatureGreen Chemistry TechnologyTransmission electron microscopyNanoparticlesSpectrophotometry UltravioletPalladiumNuclear chemistryPalladiumBromobenzenesDalton transactions (Cambridge, England : 2003)
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Plant Microtechnique and Microscopy

2001

ChromatographyStructural BiologyChemistryMicrotechniqueMicroscopyGeneral Physics and AstronomyGeneral Materials ScienceCell BiologyMicron
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Keyhole limpet hemocyanin (KLH), I: Reassociation from Immucothel® followed by separation of KLH1 and KLH2

1997

Abstract Studies of keyhole limpet hemocyanin (KLH) normally require purification of functional complexes directly from living animals. An alternative procedure is described wherein a commercial preparation of KLH which is fully dissociated into its subunits (Immucothel®, biosyn Arzneimittel GmbH) is reassociated in the presence of a high concentration of calcium and magnesium. The reassociation products, when observed by electron microscopy, consist of didecamers, multidecamers and flexible tubules of varying length. The two forms of KLH described previously and designated KLH1 and KLH2, are present in the reassocated mixture as homo-oligomers/polymers and can be separated by selective dis…

ChromatographybiologyMacromolecular SubstancesElutionProtein subunitSize-exclusion chromatographyGeneral Physics and AstronomyCell BiologyMegathura crenulatabiology.organism_classificationNegative stainRespiratory proteinMicroscopy ElectronMolluscaStructural BiologyHemocyaninsPEG ratioChromatography Gelbiology.proteinAnimalsIndicators and ReagentsGeneral Materials ScienceCrystallizationKeyhole limpet hemocyaninMicron
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Removal of trivalent chromium from tannery waste waters using bone charcoal

2002

International audience; The ability of bone charcoal to remove Cr(III) from aqueous solutions by adsorption has been investigated. The adsorbent used was first characterised and then the adsorption was studied as a function of time and amount of charcoal. Tests were carried out with synthetic solutions whose Cr concentrations (500 mg L-1) were similar to those found in some effluents of Moroccan tannery industries. Cr removal efficiencies higher than 90% were obtained at pH 3.5 using 3 g of bone charcoal and a stirring time of about 30 min. Results of Cr removal by all sieved fractions of bone charcoal had shown the same interesting capabilities for Cr(III) retention. The cross interference…

Chromiuminorganic chemicalschemistry.chemical_elementMineralogyIndustrial WasteHydrochloric acid02 engineering and technology010501 environmental sciences01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundChromiumAdsorptionNitric acidSpecific surface areaCharcoal0105 earth and related environmental sciencesAqueous solutionSpectrophotometry Atomic[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyequipment and supplies6. Clean watercarbohydrates (lipids)MoroccochemistrySodium hydroxidevisual_artCharcoalvisual_art.visual_art_mediumMicroscopy Electron ScanningAdsorption0210 nano-technologyWater Pollutants ChemicalNuclear chemistry
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ORGANIZATION OF HIGHER-LEVEL CHROMATIN STRUCTURES (CHROMOMERE, CHROMONEMA AND CHROMATIN BLOCK) EXAMINED USING VISIBLE LIGHT-INDUCED CHROMATIN PHOTO-S…

2002

The method of chromatin photo-stabilization by the action of visible light in the presence of ethidium bromide was used for investigation of higher-level chromatin structures in isolated nuclei. As a model we used rat hepatocyte nuclei isolated in buffers which stabilized or destabilized nuclear matrix. Several higher-level chromatin structures were visualized: 100 nm globules—chromomeres, chains of chromomeres—chromonemata, aggregates of chromomeres—blocks of condensed chromatin. All these structures were completely destroyed by 2 M NaCl extraction independent of the matrix state, and DNA was extruded from the residual nuclei (nuclear matrices) into a halo. These results show that nuclear …

ChromomereLightPhotochemistrySolenoid (DNA)BuffersBiologyRadiation Dosagechemistry.chemical_compoundMicroscopy Electron TransmissionNuclear Matrix-Associated ProteinsEthidiumAnimalsNucleoidChromatin structure remodeling (RSC) complexInterphaseCell NucleusCell BiologyGeneral MedicineNuclear matrixMolecular biologyChromatinProtein Structure TertiaryRatsChromatinDNA-Binding ProteinschemistryHepatocytesBiophysicsbiology.proteinInterphaseDNASubcellular FractionsCell Biology International
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IDENTIFICATION OF LECTINS IN THE KINETIDS OFTETRAHYMENA PYRIFORMIS

1997

Previously we described lectin-like molecules in the ciliate Tetrahymena pyriformis; by application of synthetic neoglycoconjugates it is now shown that T. pyriformis contains considerable amounts of both a beta-D-glucose- and a lactose-specific lectin. No evidence for the presence of alpha-D-mannose-, alpha-D-galactose- or of alpha-L-fucose-specific lectins could be obtained. The two lectins, identified in T. pyriformis, are associated with the kinetids. During cell division the lectins disappear or become masked in the fission furrow. Therefore, we assume that these lectins are involved in the organization of the distribution pattern of the kinetids during cell division perhaps due to lec…

CiliateCell divisionbiologyTetrahymena pyriformisLectinCell BiologyGeneral Medicinebiology.organism_classificationCell biologyMicroscopy FluorescenceAlbuminsLectinsDistribution patternTetrahymena pyriformisbiology.proteinAnimalsIdentification (biology)GlycoconjugatesCell DivisionFluorescein-5-isothiocyanateCell Biology International
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Détection de formes compactes en imagerie : développement de méthodes cumulatives basées sur l'étude des gradients : Applications à l'agroalimentaire

2018

The counting cells (Malassez, Thoma ...) are designed to allow the enumeration of cells under a microscope and the determination of their concentration thanks to the calibrated volume of the grid appearing in the microscopic image. Manual counting has major disadvantages: subjectivity, non-repeatability ... There are commercial automatic counting solutions, the disadvantage of which is that a well-controlled environment is required which can’t be obtained in certain studies ( eg glycerol greatly affects the quality of the images ). The objective of the project is therefore twofold: an automated cell count and sufficiently robust to be feasible regardless of the acquisition conditions.In a f…

CircleDetectionMicroscopy[INFO.INFO-CV] Computer Science [cs]/Computer Vision and Pattern Recognition [cs.CV][ INFO.INFO-TS ] Computer Science [cs]/Signal and Image Processing[INFO.INFO-TS]Computer Science [cs]/Signal and Image Processing[INFO.INFO-TS] Computer Science [cs]/Signal and Image ProcessingCercleImageMalassez[INFO.INFO-CV]Computer Science [cs]/Computer Vision and Pattern Recognition [cs.CV]Microscopie[ INFO.INFO-CV ] Computer Science [cs]/Computer Vision and Pattern Recognition [cs.CV]
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Entrapment of A Beta 1-40 peptide in unstructured aggregates

2012

Recognizing the complexity of the fibrillogenesis process provides a solid ground for the development of therapeutic strategies aimed at preventing or inhibiting protein-protein aggregation. Under this perspective, it is meaningful to identify the possible aggregation pathways and their relative products. We found that Aβ-peptide dissolved in a pH 7.4 solution at small peptide concentration and low ionic strength forms globular aggregates without typical amyloid β-conformation. ThT binding kinetics was used to monitor aggregate formation. Circular dichroism spectroscopy, AFM imaging, static and dynamic light scattering were used for structural and morphological characterization of the aggre…

Circular dichroismAmyloidKineticsPeptideProtein Structure SecondaryFIBRIL FORMATIONDynamic light scatteringMEMBRANE DISRUPTIONGeneral Materials ScienceFiberATOMIC-FORCE MICROSCOPYchemistry.chemical_classificationAmyloid beta-PeptidesChemistryProtein StabilityOsmolar ConcentrationTemperatureFibrillogenesisCondensed Matter PhysicsReceptor–ligand kineticsPeptide FragmentsAMYLOID-BETA-PROTEINALZHEIMERS-DISEASECrystallographyKineticsSpectrometry FluorescenceBiophysicsProtein Multimerization
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