Search results for "Labeling"

showing 10 items of 372 documents

Immunoelectron Microscopy of Vesicle Transport to the Primary Cilium of Photoreceptor Cells

2009

Cilia are organelles of high structural complexity. Since the biosynthetic machinery is absent from cilia all their molecular components must be synthesized in organelles of the cytoplasm and subsequently transported to the cilium. Ciliary cargos are thought to be translocated in the membrane of transport vesicles or association with these vesicles to the base of the cilium where the vesicles fuse with the periciliary target membrane for further delivery of their cargo into the ciliary compartment by the intraflagellar transport (IFT). Here we describe a modified preembedding labeling method as an alternative technique to conventional postembedding methods eligible for analyses of ciliary c…

Vesicular transport proteinImmunolabelingCytoplasmIntraflagellar transportCiliumVesicleImmunoelectron microscopyOrganellesense organsBiologyCell biology
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Short term adaptive response of symbiotic N2 fixation in pea to root pruning of half the root system, linked to the availability of carbon assimilates

2014

Symbiotic N fixation of legumes is very sensitive to environmental stresses, like pea pests damaging nodulated roots. However, the impact on their N uptake capacity and plant growth has not been studied so far.We analyzed the adaptive response symbiotic N2 fixation and plant growth of pea wild type Frisson and hypernodulating mutants P64, P118 and P121 mutated respectively on genes SYM28, SYM29 and NOD3 to root pruning of half the root system at the end of the vegetative stage. The adaptive responses of pea: cv. Frisson and 3 of its hypernodulating mutants were compared under varying carbon supplies from photosynthesis.At 380 ppm, mutant P118 showed the lowest decrease of the specific activ…

[ SDV.BV ] Life Sciences [q-bio]/Vegetal BiologyC Assimilation and partitioningNodules15NRacinesMarquage isotopique 13CPisum sativum L.AblationRootsMutants hypernodulantsFixation symbiotique du N2Low or elevated CO2 concentrationSink strength for CTeneur en CO2 faible ou élevéeForce de puits pour le carboneSymbiotic N2fixation15N Isotopic labeling[SDV.BV]Life Sciences [q-bio]/Vegetal Biology[SDV.BV] Life Sciences [q-bio]/Vegetal BiologyHypernodulating mutantsRoot pruning13CAssimilation et répartition du CNodosités
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A Note on Radio Antipodal Colouring of Paths

2005

International audience; The radio antipodal number of a graph G is the smallest integer c such that there exists an assignment f : V (G) -> {1, 2, . . . , c} satisfying |f(u) − f(v)| >= D − d(u, v) for every two distinct vertices u and v of G, where D is the diameter of G. In this note we determine the exact value of the antipodal number of the path, thus answering the conjecture given in [G. Chartrand, D. Erwin, and P. Zhang. Radio antipodal colorings of graphs, Math. Bohem. 127(1):57-69, 2002]. We also show the connections between this colouring and radio labelings.

[INFO.INFO-DM] Computer Science [cs]/Discrete Mathematics [cs.DM]MSC 05C78 05C12 05C15[ INFO.INFO-DM ] Computer Science [cs]/Discrete Mathematics [cs.DM]distance labeling[INFO.INFO-DM]Computer Science [cs]/Discrete Mathematics [cs.DM]radio numberradio antipodal colouring
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Réponses adaptatives du Pois protéagineux à une perturbation de la fixation symbiotique d'azote en relation avec le métabolisme carboné

2013

[SDE] Environmental Sciences[SDV]Life Sciences [q-bio]RacinesPisum sativum L.Marquage isotopique 13CAblationMutants hypernodulantsnodositésFixation symbiotique du N2[SDV] Life Sciences [q-bio]Teneur en CO2 faible ou élevéeForce de puits pour le carbone15N Isotopic labeling[SDE]Environmental SciencesAssimilation et répartition du C
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Analysis of fluorescent MRI contrast agent behavior in the liver and thoracic aorta of mice.

2004

To characterize the behavior of magnetofluorescent products injected in mice intravenously.The magnetic resonance imaging (MRI) products were labelled with fluorescent molecules to examine the biodistribution process in vivo and observe them at the cellular level by means of confocal microscopy. Three-dimensional (3D) sequences of images were obtained by spectral analysis of sample preparations in a multiphoton confocal microscope and analyzed by the factor analysis of medical image sequence algorithm, which provides factor curves. Factor images are the result of image-processing methods that utilize information from emission spectra. Preparations are also screened in the counting mode to p…

[SDV.IB.IMA]Life Sciences [q-bio]/Bioengineering/ImagingContrast MediaAorta ThoracicMiceMESH : Image CytometryMESH: Microscopy ConfocalMESH : FemaleMESH : Fluorescent DyesMESH: AnimalsMESH : Algorithms[ SDV.IB.IMA ] Life Sciences [q-bio]/Bioengineering/Imaginghealth care economics and organizationsImage CytometryMice Inbred BALB CMicroscopy ConfocalMESH: Fluorescent DyesMESH: Staining and LabelingLiverMESH : MeglumineFemaleMESH : Organometallic CompoundsAlgorithmsMESH: Aorta ThoraciceducationMESH: Mice Inbred BALB CMESH: AlgorithmsMESH: MeglumineMESH : Staining and LabelingMeglumineMESH: Contrast MediaMESH : MiceOrganometallic CompoundsAnimalsMESH : Microscopy ConfocalMESH: MiceMESH : Mice Inbred BALB CFluorescent DyesMESH : Aorta ThoracicMESH : Contrast MediaStaining and LabelingMESH : LiverMESH: Organometallic CompoundsMESH : Xanthenes[SDV.IB.IMA] Life Sciences [q-bio]/Bioengineering/ImagingXanthenesMESH: XanthenesMESH : AnimalsMESH: FemaleMESH: Image CytometryMESH: Liver
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A novel homologous model for noninvasive monitoring of endometriosis progression.

2017

To date, several groups have generated homologous models of endometriosis through the implantation of endometrial tissue fluorescently labeled by green fluorescent protein (GFP) or tissue from luciferase-expressing transgenic mice into recipient animals, enabling noninvasive monitoring of lesion signal. These models present an advantage over endpoint models, but some limitations persist; use of transgenic mice is laborious and expensive, and GFP presents poor tissue penetration due to the relatively short emission wavelength. For this reason, a homologous mouse model of endometriosis that allows in vivo monitoring of generated lesions over time and mimics human lesions in recipient mice wou…

adenoviral labeling0301 basic medicineGenetically modified mousein vivo monitoringPathologymedicine.medical_specialtynoninvasive modelEndometriosisEndometriosisMice Transgenichomologous mouse modelBiologyEndometriumGreen fluorescent proteinLesion03 medical and health sciencesEndometriumMiceendometriotic lesionsIn vivomedicineAnimalsHumansNeovascularization PathologicDecidualizationCell BiologyGeneral Medicinemedicine.diseaseMice Inbred C57BLDisease Models AnimalLuminescent Proteins030104 developmental biologymedicine.anatomical_structureReproductive MedicineMicroscopy FluorescenceDisease ProgressionFemalemedicine.symptommCherryBiology of reproduction
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Covalent modificaition of juvenile hormone binding proteins by photoaffinity labeling: An unexpected gel shift effect

1994

The 32 kD juvenile hormone binding protein (JHBP) and two 80 kD proteins in larval Manduca sexta hemolymph were labeled with [3H]FDK, a photoaffinity analog of methyl farnesoate (MF). The labeling could be completely displaced by a 30-fold excess of either MF or JH II, demonstrating that [3H]FDK binds specifically to the JH binding sites of the 32 kD JHBP and the 80 kD proteins. In addition, a high molecular-mass protein was labeled with [3H]FDK; labeling could be displaced by excess MF but not by JH II, demonstrating the selectivity in binding MF. The 32 kD JHBP also appeared to weakly bind the potent juvenoid, methoprene, at the JH binding site. Covalent modification by [3H]FDK induced a …

chemistry.chemical_classificationAffinity labelinghemolymphPhotoaffinity labelingPhysiologyBinding proteinmethoprene analogGeneral MedicineBiologyLigand (biochemistry)BiochemistryAmino acidmanduca sextaIsoelectric pointmethyl farnesoatechemistryBiochemistryInsect ScienceJuvenile hormoneJH II analogBinding siteArchives of Insect Biochemistry and Physiology
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3'-Arylazido-beta-alanyl-2-azido ATP, a cross-linking photoaffinity label for F1ATPases.

1989

Abstract The synthesis of the 3′-arylazido-2-azido ATP derivative 3′-O-{3-[N-(4-azido-2-nitrophenyl)-amino]propionyl}2-azido-adenosine 5′-triphosphate (2,3′-DiN3ATP) is described. The bifunc­ tional photoreactive ATP analog is characterized spectroscopically. Photoaffinity labeling of F, ATPase from Micrococcus luteus by this analog results in the inactivation of the enzyme and in the formation of higher molecular weight cross-links,

chemistry.chemical_classificationAzidesPhotoaffinity labelingbiologyLightStereochemistryAffinity Labelsbiology.organism_classificationGeneral Biochemistry Genetics and Molecular BiologyMicrococcuschemistry.chemical_compoundKineticsProton-Translocating ATPasesEnzymeAdenosine TriphosphatechemistryIndicators and ReagentsBifunctionalBeta (finance)Micrococcus luteusDerivative (chemistry)Zeitschrift fur Naturforschung. C, Journal of biosciences
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Radioactive labeling of defined HPMA-based polymeric structures using [18F]FETos for in vivo imaging by positron emission tomography.

2009

During the last decades polymer-based nanomedicine has turned out to be a promising tool in modern pharmaceutics. The following article describes the synthesis of well-defined random and block copolymers by RAFT polymerization with potential medical application. The polymers have been labeled with the positron-emitting nuclide fluorine-18. The polymeric structures are based on the biocompatible N-(2-hydroxypropyl)-methacrylamide (HPMA). To achieve these structures, functional reactive ester polymers with a molecular weight within the range of 25,000-110,000 g/mol were aminolyzed by 2-hydroxypropylamine and tyramine (3%) to form (18)F-labelable HPMA-polymer precursors. The labeling procedure…

chemistry.chemical_classificationBiodistributionAcrylamidesFluorine RadioisotopesPolymers and PlasticsPolymersRadical polymerizationSize-exclusion chromatographyRadiochemistryBioengineeringChain transferPolymerPolymerizationRatsBiomaterialsPolymerizationchemistryIsotope LabelingPositron-Emission TomographyPolymer chemistryMaterials ChemistryAnimalsReversible addition−fragmentation chain-transfer polymerizationPreclinical imagingBiotransformationBiomacromolecules
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Negative Staining of Thinly Spread Biological Samples

2007

Negative staining is widely applicable to isolated viruses, protein molecules, macro-molecular assemblies and fibrils, subcellular membrane fractions, liposomes and artificial membranes, synthetic DNA arrays, and also to polymer solutions. In this chapter, techniques are provided for the preparation of the necessary support films (continuous carbon and holey/perforated carbon). The range of suitable negative stains is presented, with some emphasis on the benefit of using ammonium molybdate and of negative stain-trehalose combinations. Protocols are provided for the single-droplet negative staining technique (on continuous and holey carbon support films), the negative staining-carbon film te…

chemistry.chemical_classificationChemistryUranyl acetatePolymerNegative stainlaw.inventionStainingchemistry.chemical_compoundImmunolabelingMembranelawTannic acidBiophysicsCrystallization
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