Search results for "agarose"

showing 10 items of 64 documents

MboII endonuclease heat inactivation before agarose gel electrophoresis to prevent artifactual bands in restriction patterns

1999

Gel electrophoresisDNA BacterialElectrophoresis Agar GelProtein DenaturationSettore MED/07 - Microbiologia E Microbiologia ClinicaHot TemperaturebiologyMolecular biologyGeneral Biochemistry Genetics and Molecular BiologyRestriction fragmentHeat inactivationElectrophoresischemistry.chemical_compoundRestriction enzymeBiochemistrychemistryAgarose gel electrophoresisEnzyme Stabilitybiology.proteinEscherichia coliDeoxyribonucleases Type II Site-SpecificMboII endonucleaseDNAPolymorphism Restriction Fragment LengthBiotechnology
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Orthogonal electrophoretic fractionation of DNA in agarose gels.

2008

We developed an electrophoretic procedure, using Voltage Gradient Gel Electrophoresis (VGGE), which allows to obtain both an improvement of the resolution power of the system in orthogonal fractionation of DNA and, mainly, an about fourfold enhancement of hybridization signals in Southern blotting applications.

Gel electrophoresisElectrophoresis Agar GelChromatographyGel electrophoresis of nucleic acidsCell BiologyFractionationDNABiologyMolecular biologyInterleukin-10chemistry.chemical_compoundElectrophoresischemistryAgaroseRNA MessengerMolecular BiologyDNATemperature gradient gel electrophoresisSouthern blotMolecular and cellular probes
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Voltage gradient electrophoresis of nucleic acids on agarose gels.

1993

A very simple method is described which allows the separation of DNA molecules in a wide molecular weight range (from 0.6 to about 30 kb) in the same electrophoresis agarose gel. This is based on the achievement of a voltage gradient through a simple device consisting of a Plexiglas plate placed slantwise with respect to the gel surface plane, submerged in the electrophoretic running buffer. Further applications of our system are also described.

Gel electrophoresisElectrophoresis Agar GelChromatographyGel electrophoresis of nucleic acidsChemistryBiophysicsCell BiologyDNABiochemistryBuffer (optical fiber)Molecular WeightElectrophoresischemistry.chemical_compoundEvaluation Studies as TopicAgarose gel electrophoresisPulsed-field gel electrophoresisNucleic acidAgaroseMolecular BiologyPlasmidsAnalytical biochemistry
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Use of voltage gradient gel electrophoresis in apoptotic DNA analysis

2000

In this paper the use of voltage gradient gel electrophoresis (VGGE) in the electrophoretic analysis of apoptotic DNAs is described. The peculiarity of VGGE fractionation in enhancing DNA bands in the gel by reducing their thickness was used to obtain a rapid, more selective and higher-quality electrophoretic fractionation of apoptotic DNA with respect to conventional electrophoresis. The use of VGGE fractionations also allowed a reduced amount of DNA to be used to detect a characteristic apoptotic DNA ladder pattern, in a lower agarose gel concentration, with respect to conventional electrophoretic fractionation

Gel electrophoresisInsectaChromatographyGel electrophoresis of nucleic acidsChemistryOrganic ChemistryApoptosisDNAGeneral MedicineFractionationBiochemistryAnalytical ChemistryElectrophoresischemistry.chemical_compoundElectricityMolecular-weight size markerPulsed-field gel electrophoresisAnimalsAgaroseElectrophoresis Polyacrylamide GelDNAJournal of Chromatography A
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Multiple voltage‐gradient gel electrophoresis system

2001

A new device, based on the principle of voltage-gradient gel electrophoresis, was developed in order to enhance differentiation of the distance across the range of molecular masses in the electrophoretic fractionation of nucleic acids in an agarose matrix. The apparatus has a series of modular parallel plates, placed slantwise to allow reiteration of the voltage gradient effect along the gel. This subjects DNA fragments of variable length to differential runnings according to their original position in the gel. Both the number of slantwise plates and the distance between them can be changed to modify operating performance. Our system allows better fractionations as compared to conventional …

Gel electrophoresisTwo-dimensional gel electrophoresisGel electrophoresis of nucleic acidsDifference gel electrophoresisClinical BiochemistryAnalytical chemistryBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryElectrochromatographyMolecular-weight size markerPulsed-field gel electrophoresisAgaroseELECTROPHORESIS
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Proteoglycan synthesis by cultured human chondrocytes.

1994

Iliac crest biopsies are important in the detection of human skeletal dysplasias. Therefore, culture of these cells may serve as a valuable method for studying proteoglycan metabolism in chondrocytes of individuals with skeletal abnormalities. Morphological and biochemical studies were performed on human iliac crest chondrocytes grown in monolayer and in agarose gels. Two proteoglycan populations of different hydrodynamic size and glycosaminoglycan composition were synthesized by cells grown in monolayer. Chondrocytes cultured in an agarose gel for 2 weeks synthesized proteoglycans identical to those of the native tissue with respect to hydrodynamic size and glycosaminoglycan chain length. …

HistologyAscorbic AcidChondrocyteGlycosaminoglycanIliumchemistry.chemical_compoundmedicineHumansInstrumentationCells CulturedGlycosaminoglycansbiologyChemistryCartilageSepharoseChondroitin SulfatesInfant NewbornCell DifferentiationAscorbic acidCell biologycarbohydrates (lipids)Medical Laboratory Technologymedicine.anatomical_structureCartilageBiochemistryProteoglycanChondroitin Sulfate ProteoglycansCell culturebiology.proteinUltrastructureChromatography GelAgaroseAnatomyMicroscopy research and technique
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Reversibly stable thiopolyplexes for intracellular delivery of genes.

2006

Novel polyaspartamide non-viral carriers for gene therapy were synthesized by introducing, on the same polymer backbone, positively charged groups, for electrostatic interactions with DNA, and thiol groups for the formation of disulfide bridges between polymer chains. The introduction of thiols was aimed to have a vector with low redox potential sensitivity: disulfide crosslinking in fact, being stable in extracellular environment, allowed either to have stable complexes in plasma, that can protect DNA from metabolism, or to be reduced inside the cell, where the excess of glutathion in reduced form maintains a low redox potential. The consequent destabilization of the complex after disulfid…

Magnetic Resonance SpectroscopyLightStereochemistryCell SurvivalPolymersPharmaceutical ScienceElectrophoretic Mobility Shift AssayGene deliveryTransfectionchemistry.chemical_compoundGene DeliveryMiceDynamic light scatteringGenes ReporterCell Line TumorAnimalsScattering RadiationElectrophoretic mobility shift assayDisulfidesSulfhydryl CompoundsLuciferaseschemistry.chemical_classificationthiopolycationsEndodeoxyribonucleasesLuminescent AgentsGenetic transferCationic polymerizationProteinsDNAChromatography Ion ExchangeCombinatorial chemistrychemistrypolyaspartammideAgarose gel electrophoresisThiolPeptidesOxidation-ReductionDNAJournal of controlled release : official journal of the Controlled Release Society
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A discoidal lipoprotein from the coelomic fluid of the polychaete Nereis virens.

2005

A discoidal lipoprotein was isolated from the coelomic fluid of the polychaete, Nereis virens, by density gradient centrifugation. The lipoprotein was present in both sexes and moved as a uniform band in an agarose gel. The average diameter of the lipoprotein particles determined by electron microscopy was 42 nm with a thickness of 10 nm. SDS electrophoresis showed two apoprotein subunits with molecular masses of 247 and 85 kDa, respectively. In lectin blots, both apoproteins were reactive with Concanavalin A indicating the presence of N-glycans. The small subunit was also reactive with peanut lectin, indicating additional O-glycosylation. The total lipid content was 48% and consisted mainl…

MaleEmbryo NonmammalianGlycosylationPhysiologyLipoproteinsBiologyIn Vitro TechniquesBiochemistrychemistry.chemical_compoundPolysaccharidesAnimalsParticle SizeMolecular BiologyDifferential centrifugationMolecular massLectinPolychaetaLipidsThin-layer chromatographyBody FluidsMolecular WeightElectrophoresisProtein SubunitschemistryBiochemistryConcanavalin Abiology.proteinAgaroselipids (amino acids peptides and proteins)FemaleLipoproteinComparative biochemistry and physiology. Part B, Biochemistrymolecular biology
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Comparison of the metabolism of 7-ethoxycoumarin and coumarin in precision-cut rat liver and lung slices

1995

The metabolism of 7-ethoxycoumarin and [3-(14)C]coumarin was compared in precision-cut rat liver and lung slices. The lung slices were prepared using an agarose gel instilling technique enabling the production of tissue cylinders followed by lung slices employing a Krumdieck tissue slicer. Both 50 microM 7-ethoxycoumarin and 50 microM [3-(14)C]coumarin were metabolized by rat liver and lung slices. 7-Ethoxycoumarin was converted to 7-hydroxycoumarin (7-HC) which was conjugated with both D-glucuronic acid and sulfate. 7-HC sulfate was the major metabolite formed by both liver and lung slices. [3-(14)C]Coumarin was metabolized by rat liver and lung slices to both polar products and to metabol…

MaleMetaboliteGlucuronatesBiologyToxicologyRats Sprague-Dawleychemistry.chemical_compoundGlucuronic AcidCoumarinsCulture TechniquesmedicineAnimalsUmbelliferonesLungLungSulfatesCytochrome P450General MedicineMetabolismCoumarinGlucuronic acidRatsmedicine.anatomical_structureLiverchemistryBiochemistryIsotope Labelingbiology.proteinAgaroseDrug metabolismFood ScienceFood and Chemical Toxicology
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Ag nanoparticles agargel nanocomposites for SERS detection of cultural heritage interest pigments

2018

Agarose gel (agargel) composites with commercial and laboratory made silver nanoparticles were prepared by a wet solution method at room temperature. The gel composites were used for pigment extraction and detection by Raman spectroscopy. Red (alizarin) and violet (crystal violet) pigments deposited on paper were extracted by the composites and were investigated by micro-Raman spectroscopy. Evaluation was carried out of the surface-enhanced Raman spectroscopy (SERS) effect induced by the silver nanoparticles embedded in the gel. A kinetic approach as a function of time was used to determine the efficiency of pigments extraction by composites deposition. A non-invasive extraction process of …

Materials scienceNanocompositeExtraction (chemistry)General Physics and Astronomy02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyAlizarin01 natural sciencessers cultural heritage raman spectroscopySilver nanoparticle0104 chemical scienceschemistry.chemical_compoundsymbols.namesakechemistrySurface Enhanced Raman Spectroscopy Cultural Heritage pigmentssymbolsAgarosesense organsCrystal violet0210 nano-technologyRaman spectroscopySpectroscopyNuclear chemistryThe European Physical Journal Plus
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