Search results for "Electrophoresi"

showing 10 items of 1009 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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Enhanced hybridization labeling signals in Southern blotted DNAs fractionated with voltage gradient gel electrophoresis.

1998

An enhancement of hybridization labeling signals is demonstrated in Southern blotted DNAs, fractionated by voltage gradient gel electrophoresis. This enhancement is due to a reduced thickness of each single nucleic acid band in the gel as a consequence of the gradient effect, corresponding to an increased concentration of DNA per unit area.

Gel electrophoresisElectrophoresis Agar GelChromatographyGel electrophoresis of nucleic acidsClinical BiochemistryVoltage gradientMembrane ProteinsNucleic Acid HybridizationDNAChemical FractionationBiochemistryAnalytical Chemistrychemistry.chemical_compoundBlotting SouthernchemistryMolecular-weight size markerSea UrchinsNucleic acidPulsed-field gel electrophoresisElectrochemistryAnimalsDNASouthern blotElectrophoresis
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Acquisition of thermotolerance in sea urchin embryos correlates with the synthesis and age of the heat shock proteins.

1986

Preheating at 31 degrees C induces thermotolerance in Paracentrotus lividus embryos, which therefore become able to withstand 1-h treatment at the otherwise lethal temperature of 35 degrees C, and to develop normally. The acquisition of thermotolerance is positively correlated with the amount of heat shock proteins produced during the 31 degrees C treatment. Evidence is provided that the heat shock proteins, although present in the embryo for long periods after synthesis, lose their effect on thermotolerance within 3 h of the cessation of synthesis.

Gel electrophoresisEmbryo NonmammalianbiologyEcologyAcclimatizationTemperatureEmbryoMetabolismGastrulaSea urchin embryobiology.organism_classificationParacentrotus lividusCell biologybiology.animalHeat shock proteinSea UrchinsAnimalsFemaleSea urchinHeat-Shock ProteinsDevelopmental BiologyCell differentiation
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Lipid Rafts in Higher Plant Cells

2004

A large body of evidence from the past decade supports the existence of functional microdomains in membranes of animal and yeast cells, which play important roles in protein sorting, signal transduction, or infection by pathogens. They are based on the dynamic clustering of sphingolipids and cholesterol or ergosterol and are characterized by their insolubility, at low temperature, in nonionic detergents. Here we show that similar microdomains also exist in plant plasma membrane isolated from both tobacco leaves and BY2 cells. Tobacco lipid rafts were found to be greatly enriched in a sphingolipid, identified as glycosylceramide, as well as in a mixture of stigmasterol, sitosterol, 24-methyl…

Gel electrophoresisErgosterolNADPH oxidasebiologyCell Biologymedicine.disease_causeBiochemistrySphingolipidCell biologychemistry.chemical_compoundMembranechemistryMembrane proteinBiochemistryProtein targetingmedicinebiology.proteinlipids (amino acids peptides and proteins)Molecular BiologyLipid raftJournal of Biological Chemistry
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Proteomic analysis of the photosystem I light-harvesting antenna in tomato (Lycopersicon esculentum).

2004

Until now, more genes of the light-harvesting antenna of higher-plant photosystem I (PSI) than proteins have been described. To improve our understanding of the composition of light-harvesting complex I (LHCI) of tomato (Lycopersicon esculentum), we combined one- and two-dimensional (1-D and 2-D, respectively) gel electrophoresis with immunoblotting and tandem mass spectrometry (MS/ MS). Separation of PSI with high-resolution 1-D gels allowed separation of five bands attributed to proteins of LHCI. Immunoblotting with monospecific antibodies and MS/MS analysis enabled the correct assignment of the four prominent bands to light-harvesting proteins Lhcal -4. The fifth band was recognized by o…

Gel electrophoresisGene isoformElectrophoresisProteomicsChromatographybiologyPhotosystem I Protein ComplexImmunoblottingMolecular Sequence DataLight-Harvesting Protein ComplexesContext (language use)Tandem mass spectrometrybiology.organism_classificationPhotosystem IBiochemistryLycopersiconMass SpectrometryIsoelectric pointBiochemistrySolanum lycopersicumSequence Analysis ProteinProtein IsoformsAmino Acid SequencePhotosystemBiochemistry
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Analysis of myxoma virus genome using pulsed-field gel electrophoresis

1996

A method is presented for the isolation of large quantities of myxoma virus DNA using pulsed-field gel electrophoresis (PFGE), and some preliminary applications of this technique.

Gel electrophoresisGeneral Veterinarybiology[SDV]Life Sciences [q-bio]Myxoma virusMyxoma virusGenome ViralPoxviridae InfectionsGeneral Medicinebiology.organism_classificationMicrobiologyGenomeDNA extractionVirologyMolecular biologyVirusElectrophoresis Gel Pulsed-Field[SDV] Life Sciences [q-bio]DNA Viralcardiovascular systemPulsed-field gel electrophoresisAnimalsPoxviridaeRabbitsLeporipoxvirus
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2001

Eight strains of Taylorella equigenitalis were identified by a polymerase chain reaction using a primer pair specific to the 16S rDNA of T. equigenitalis. These eight strains were chosen because they had previously been shown to represent eight distinct genotypes by pulsed-field gel electrophoresis analysis after separate digestion of the genomic DNA with ApaI or NotI. The eight strains could be classified into six or seven types by random amplified polymorphic DNA analysis using different kinds of primers. Amplified rDNA restriction analysis after separate digestion with five restriction enzymes, including AluI and MboI, of the 1500 bp fragments of rDNA amplified by polymerase chain reacti…

Gel electrophoresisGeneticsGeneral VeterinarybiologyGeneral Medicinebiology.organism_classificationMolecular biologyAmplified Ribosomal DNA Restriction AnalysisRestriction enzymeTaylorella equigenitalisCleaved amplified polymorphic sequencePulsed-field gel electrophoresisAmplified fragment length polymorphismRestriction fragment length polymorphismVeterinary Research Communications
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A Comparative Study of Different Methods of Yeast Strain Characterization

1992

Summary An extensive survey of different methods of yeast strain identification (classical microbiological tests, whole-cell protein electrophoresis, chromosomal patterns, DNA hybridization and mitochondrial DNA restriction analysis) has been carried out in order to differentiate, with industrial purposes, strains present in the Alicante wine ecosystem. Only chromosomal patterns and mitochondrial DNA (mtDNA) restriction analysis show differences between strains. Both techniques are very complex to be used in bio technological industries. For this reason, we have developed a new, simple, unexpensive and rapid method based on mtDNA restriction analysis.

Gel electrophoresisGeneticsMitochondrial DNAbiologyDNA–DNA hybridizationSaccharomyces cerevisiaebiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologyYeastRestriction fragmentYeast in winemakingRestriction mapbiology.proteinEcology Evolution Behavior and SystematicsSystematic and Applied Microbiology
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