Search results for "Gel electrophoresi"

showing 10 items of 321 documents

Keyhole limpet haemocyanin (KLH): Purification of intact KLH1 through selective dissociation of KLH2

1995

Abstract Keyhole limpet haemocyanin (KLH) from almost all newly captive animals contains a mixture of KLH1 and KLH2. We show that the dissociation of KLH2 can be produced during EM specimen preparation by the negative staining-carbon film (NS-CF) procedure and in solution by ammonium molybdate-PEG solutions at slightly acidic pHs. The KLH2 multidecamers split apart in the pH range 7.5-6.5 and in the pH range 6.5-6.0 the individual decamers break open and start to dissociate. At pH 5.9 the dissociation of KLH2 yields predominantly a mixture of single subunits and what appear to be subunit dimers. Over the pH range 7.0-5.7 the KLH1 didecamer remains stable. Separation of intact KLH1, in the f…

Gel electrophoresisChromatographybiologySize-exclusion chromatographyGeneral Physics and AstronomyCell BiologyMegathura crenulatabiology.organism_classificationNegative stainDissociation (chemistry)Respiratory proteinchemistry.chemical_compoundchemistryStructural Biologybiology.proteinGeneral Materials ScienceAmmoniumKeyhole limpet hemocyaninMicron
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The tetrameric α-helical membrane protein GlpF unfolds via a dimeric folding intermediate.

2011

Many membrane proteins appear to be present and functional in higher-order oligomeric states. While few studies have analyzed the thermodynamic stability of α-helical transmembrane (TM) proteins under equilibrium conditions in the past, oligomerization of larger polytopic monomers has essentially not yet been studied. However, it is vital to study the folding of oligomeric membrane proteins to improve our understanding of the general mechanisms and pathways of TM protein folding. To investigate the folding and stability of the aquaglyceroporin GlpF from Escherichia coli, unfolding of the protein in mixed micelles was monitored by steady-state fluorescence and circular dichroism spectroscopy…

Gel electrophoresisCircular dichroismProtein FoldingChemistryCircular DichroismEscherichia coli ProteinsMembrane ProteinsAquaporinsBiochemistryMicelleTransmembrane proteinProtein Structure SecondaryFolding (chemistry)CrystallographyKineticsMembrane proteinBiophysicsEscherichia coliProtein foldingChemical stabilityDimerizationProtein UnfoldingBiochemistry
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Computer-aided calculation of the molecular size of nondenatured proteins in pore-gradient gel electrophoresis

1991

A computer program written in Turbo C is described, which uses the two-step mathematical procedure published recently (Rothe, G. M., Electrophoresis 1988, 9, 307-316) to evaluate the molecular mass, Stokes' radius, spherical radius, and frictional coefficient of nondenatured proteins. The program runs on any IBM-PC or 100% compatible IBM-PC, provided the disk operating system MS-DOS or PC-DOS 3.0 or later has been installed. Functions that are permanently in use are accessible by menu. Storage and loading of data from disk and help instructions can be called by use of function keys. The program provides several tables into which inserted and calculated data is automatically integrated. Each…

Gel electrophoresisComputer programChemistryClinical BiochemistryAnalytical chemistryProteinsCharacter encodingRadiusFunction (mathematics)Table (information)BiochemistryDisk operating systemAnalytical ChemistryComputational scienceMolecular WeightModels ChemicalComputer-aidedElectrophoresis Polyacrylamide GelMathematicsSoftwareElectrophoresis
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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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