Search results for "Gel electrophoresi"

showing 10 items of 321 documents

DNA polymorphism of the human complement C8 beta gene: formal genetics and intragenic localization.

1989

The eighth component of human complement consists of three subunits of different molecular mass, which are coded for by three separate genetic loci. Polymorphisms have been described at the protein level for the alpha and beta subunits by means of sodium dodecyl sulfate gel electrophoresis and isoelectric focusing. Using a full-length human C8 beta cDNA probe, we have studied more than 100 individuals by Southern blot analysis to detect DNA polymorphisms. We have found two restriction fragment length polymorphisms (RFLPs) with the enzymes Taq I and Bam HI. The Taq I polymorphism is defined by two alleles, i.e., a single 4.9 kb fragment or two 2.8/2.1 kb fragments. The allele frequencies are…

GeneticsGel electrophoresisDeoxyribonuclease BamHIImmunologyBiologyMolecular biologyComplement C8Restriction fragmentBlotting SouthernGene mappingComplementary DNAGeneticsbiology.proteinHumansRestriction fragment length polymorphismDeoxyribonucleases Type II Site-SpecificGeneAllele frequencyAllelesPolymorphism Restriction Fragment LengthSouthern blotImmunogenetics
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Characterization of the Proteomic and Genomic Profiles of Chronic Lymphocytic Leukemia Patients with Distinct Clinical Prognosis According to the Mut…

2005

Abstract Introduction: In recent years several molecular prognostic factors have been identified in Chronic Lymphocytic Leukemia B (B-CLL). These include mutations in the variable region of the immunoglobulin genes (IgVH), somatic mutations in the BCL6 gene (Leukemia (2004) 18, 743–746) and the expression level of CD38 and ZAP70. However its biological significance is not clear. In order to identify novel molecular markers with prognostic and therapeutic value we have analyzed the proteomic and genomic profile of 40 B-CLL patients (Binet stage A). Material and methods: 100 μg of total PBMC proteins were used for IEF followed by 2D electrophoresis. Image analysis of scanned gels was used to …

GeneticsMutationTwo-dimensional gel electrophoresisImmunologyCell BiologyHematologyBiologymedicine.disease_causeBiochemistryMolecular biologyGene expression profilingGenomic ProfileGene expressionmedicineHuman genomePeptide-mass fingerprintGeneBlood
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Exploring diversity among Spanish strains of Erwinia amylovora and possible infection sources

2007

Aims:  We have examined the intraspecific diversity of a collection of 63 Spanish strains of Erwinia amylovora, isolated from 1995 to 2001, to determine whether or not they could be grouped based on phenotypic or genotypic criteria and to investigate the sources of inoculum for fire blight dissemination in Spain. Methods and Results:  Several biochemical and molecular techniques, such as miniaturized API 20E, API 50CH, ATB G-5 and API-ZYM tests, BIOLOG metabolic fingerprinting, PCR ribotyping, pulsed-field gel electrophoresis (PFGE), minisatellite-primed PCR (MSP-PCR), random amplified polymorphic DNA (RAPD) analyses and AFLP were used. We report the first identification in Spain of the PFG…

Geneticsbiologyfood and beveragesOutbreakGeneral MedicineErwiniabacterial infections and mycosesbiology.organism_classificationApplied Microbiology and Biotechnologylaw.inventionRAPDlawparasitic diseasesGenotypeFire blightPulsed-field gel electrophoresisAmplified fragment length polymorphismPolymerase chain reactionBiotechnologyJournal of Applied Microbiology
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High resistance to X-rays and therapeutic carbon ions in glioblastoma cells bearing dysfunctional ATM associates with intrinsic chromosomal instabili…

2014

To investigate chromosomal instability and radiation response mechanisms in glioblastoma cells.We undertook a comparative analysis of two patient-derived glioblastoma cell lines. Their resistance to low and high linear energy transfer (LET) radiation was assessed using clonogenic survival assay and their intrinsic chromosome instability status using fluorescence in situ hybridization. DNA damage was analyzed by pulsed-field gel electrophoresis and by γ-H2AX foci quantification. Expression of DNA damage response proteins was assessed by immunoblot.Increased radioresistance to X-rays as well as carbon ions was observed in glioblastoma cells exhibiting high levels of naturally occurring chromo…

Genome instabilityDNA RepairDNA damageLinear energy transferHeavy Ion RadiotherapyAtaxia Telangiectasia Mutated ProteinsBiologyRadiation ToleranceCell Line TumorChromosomal InstabilityRadioresistanceChromosome instabilitymedicineHumansDNA Breaks Double-StrandedLinear Energy TransferRadiology Nuclear Medicine and imagingGel electrophoresisRadiological and Ultrasound Technologymedicine.diagnostic_testX-RaysCell CycleGenomicsMolecular biologyPhosphorylationGlioblastomaSignal TransductionFluorescence in situ hybridizationInternational Journal of Radiation Biology
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Pulsed field gel electrophoresis and genome size estimates

2015

Pulsed field gel electrophoresis (PFGE) is a quick and reliable procedure to resolve DNA molecules larger than 30 kb by applying an electric field that periodically changes direction. This technique can be used to estimate genome size of a microorganism, to reveal if a genome is circular or linear, to indicate the presence of megaplasmids, and to show if a strain contains only one or more chromosomes.

Genome sizeDNA BacterialMaterials scienceChromosomes ArchaealSettore BIO/19 - Microbiologia GeneraleGenomePlasmidchemistry.chemical_compoundPlasmidGeneticGenome ArchaealElectric fieldPulsed-field gel electrophoresisGenome sizeMolecular BiologyElectrophoresis Agar GelBase CompositionStrain (chemistry)BacteriaMulti-repliconMedicine (all)Physical Chromosome Mappingfood and beveragesChromosomes BacterialPhysical Chromosome MappingArchaeaElectrophoresis Gel Pulsed-FieldDNA ArchaealchemistryMegaplasmidBiological systemDNAGenome BacterialGenome topology
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Genotyping of Campylobacter spp.

2000

method. The major disadvantages of both of these techniques are the high number of untypeable strains and the time-consuming and technically demanding requirements of the techniques. Production and quality control of antiserum reagents for serotyping schemes are costly; consequently, these reagents are not widely available. A recently developed scheme (23) based on HS antigens in which modified antibody production and antigen detection techniques are used may be an improvement for routine use, but this scheme does not solve the problem of restricted reagent availability or the problem of the high level of nontypeability. Because of such problems, the value of serotyping techniques for natio…

GenotypeComputational biologyBiologymedicine.disease_causeApplied Microbiology and BiotechnologyRibotypingCampylobacter InfectionsPulsed-field gel electrophoresismedicineAnimalsHumansTypingGenotypingGenotyping TechniquesEcologyCampylobacterCampylobacterMinireviewsbiology.organism_classificationVirologySubtypingBacterial Typing TechniquesCampylobacter coliGenes BacterialFood ScienceBiotechnologyApplied and environmental microbiology
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Isolation and characterization of a 60-70-kD plasma membrane glycoprotein involved in the contact-dependent inhibition of growth

1990

Previous studies have shown that plasma membrane compounds are involved in the contact-dependent inhibition of growth of human diploid fibroblasts. The purification of the active plasma membrane glycoprotein is described in this report. The glycoprotein has an apparent molecular mass of 60-70 kD and, due to differential sialylation, isoelectric points between pH 5.5. and 6.2. Treatment with sialidase yielded one spot in two-dimensional gel electrophoresis with an isoelectric point of 6.3. After removal of the N-glycosidically linked oligosaccharide chains, the apparent molecular mass is reduced by approximately 22 kD. Treatment was diluted NaOH, which removes the O-glycosidically linked por…

GlycanCell CommunicationCell LineAnimalsHumansPolyacrylamide gel electrophoresisCells CulturedCytoskeletonGel electrophoresischemistry.chemical_classificationMembrane GlycoproteinsbiologyMolecular massContact InhibitionCell MembraneContact inhibitionCell BiologyArticlesFibroblastsMolecular biologyMolecular WeightMicroscopy ElectronIsoelectric pointchemistryBiochemistryCell culturebiology.proteinChromatography GelElectrophoresis Polyacrylamide GelGlycoproteinCell DivisionThe Journal of Cell Biology
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Assessment of temperature effects on beta-aggregation of native and glycated albumin by FTIR spectroscopy and PAGE: relations between structural chan…

2007

Abstract Structural modifications of bovine serum albumin (BSA) induced by heating, and the involvement of glycation of albumin in such processing were studied by using Fourier transform infrared spectroscopy (FTIR) and polyacrylamide gel electrophoresis (PAGE). For native BSA, heating treatments gave rise to β structures which were amplified to the detriment of α-helix form, and which were associated with increased aggregation. A very high correlation was obtained between FTIR Amide I band evolution and aggregation rate parameters, showing the contribution of β-form in aggregates formation. We further assessed the effect of glycation on protein sensibility to heating treatments. A reductio…

Glycation End Products AdvancedAntioxidantTime FactorsFree Radicalsmedicine.medical_treatmentBiophysicsThermal treatmentProtein aggregationBiochemistryAntioxidantsProtein Structure SecondaryStructure-Activity RelationshipGlycationSpectroscopy Fourier Transform InfraredmedicineAnimalsGlycated Serum AlbuminBovine serum albuminFourier transform infrared spectroscopyMolecular BiologyPolyacrylamide gel electrophoresisSerum AlbuminChromatographyBinding SitesbiologyChemistryAlbuminTemperatureSerum Albumin Bovinebiology.proteinCattleElectrophoresis Polyacrylamide GelCopperArchives of biochemistry and biophysics
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Differential expression and glycosylation of proteins in the rat ileal epithelium in response to Echinostoma caproni infection.

2013

Echinostoma caproni (Trematoda: Echinostomatidae) is an intestinal trematode that has been used as experimental model to investigate the factors determining the expulsion of intestinal helminths. We analyze the changes in the protein expression and glycosylation induced by E. caproni in Wistar rat, a host of low compatibility in which the parasites are rapidly rejected. To determine the changes in protein expression, two-dimensional difference gel electrophoresis was employed using protein extracts from the intestine of naïve and infected rats. The patterns of glycosylation were analyzed by lectin blotting. Those spots showing differential expression or glycosylation were analyzed by mass s…

GlycosylationGlycosylationEchinostoma caproniDifference gel electrophoresisBiophysicsIleumBiochemistryMass SpectrometryTwo-Dimensional Difference Gel Electrophoresischemistry.chemical_compoundIleumEchinostomamedicineHelminthsAnimalsIntestinal MucosaRats WistarCytoskeletonEchinostomiasisbiologyEffectorbiology.organism_classificationMolecular biologyRatsmedicine.anatomical_structureBiochemistrychemistryGene Expression RegulationFemaleTrematodaJournal of proteomics
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Evidence for the formation of covalent bonds between macromolecules in the domain of the wall of Candida albicans mycelial cells

1989

An O-glycosylated mannoprotein, after its incorporation into the wall, showed an increase in its molecular weight, due at least to its association with N-glycosidic sugar chain(s). This was shown by rendering the material soluble after partial degradation of the wall structure. At present it is unknown whether this phenomenon is due to an additional transglycosylation process or whether the partial degradation of the wall solubilizes a supramolecular structure formed between the original O-glycosylated protein which becomes linked either directly or indirectly through a protein to the N-sugar chain(s).

GlycosylationMacromolecular SubstancesBlotting WesternBiophysicsSupramolecular chemistryPolysaccharideBiochemistryFungal ProteinsCell wallCell WallCandida albicansCandida albicansMolecular Biologychemistry.chemical_classificationGel electrophoresisMembrane Glycoproteinsbiologybeta-GlucosidaseAntibodies MonoclonalGlucan 13-beta-GlucosidaseCell Biologybiology.organism_classificationMolecular Weightcarbohydrates (lipids)ProteoglycanBiochemistrychemistryCovalent bondbiology.proteinBiophysicsProtein Processing Post-TranslationalMacromoleculeBiochemical and Biophysical Research Communications
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