Search results for " fingerprint"

showing 10 items of 157 documents

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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Basic issues in forensic DNA typing

1997

DNA analysis has become the standard method in forensic stain typing (termed DNA profiling). In contrast to conventional serological methods, any human tissue or body fluid can be analysed by DNA profiling as long as it contains nucleated cells. The majority of genetic systems studied at the DNA level are derived from "non-coding" portions from the human genome, and are located either in the vicinity of expressed (coding) genes or in stretches of DNA sequences interspersing with the genes. The typing results are usually recorded as DNA fragment lengths or "alleles" indicating the number of core repeat elements for short tandem repeat systems. These typing results do not contain any useful i…

GeneticsPolymorphism GeneticGenotypeGenome HumanDNAForensic MedicineBiologyDNA FingerprintingGenomeDNA sequencingPathology and Forensic MedicinePhenotypeDNA profilingGenetic markerHumansMultilocus sequence typingMicrosatelliteHuman genomeTypingLawAllelesRepetitive Sequences Nucleic AcidForensic Science International
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A report of an international collaborative experiment to demonstrate the uniformity obtainable using DNA profiling techniques

1992

This paper describes a collaborative exercise intended to demonstrate whether uniformity of DNA profile results could be achieved between different European laboratories. It was shown that this goal can be obtained provided that a common protocol is followed (specifically the use of a common electrophoretic buffer as being the most important parameter). Generally, lower molecular weight loci (with lower molecular weight fragments) such as YNH24 perform better than higher molecular weight loci such as MS43a. The results of the exercise are discussed in relation to the objectives of the European DNA profiling group (EDNAP).

GeneticsProtocol (science)Quality ControlElectrophoresis Agar GelDNA/bloodRestriction MappingComputational biologyDNABiologySettore MED/43 - MEDICINA LEGALEDNA FingerprintingPathology and Forensic MedicineDNA profilingMulticenter studyAutoradiographyHumansRestriction fragment length polymorphismLaboratoriesLawDNA Fingerprinting/standards
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Y-chromosomal STR haplotypes in Sicily

2006

Eight Y-chromosomal short tandem repeats (STRs)-DYS19, DYS389-I, DYS389-II, DYS390, DYS391, DYS392, DYS393 and DYS385 - were typed in a population sample (n = 255) of unrelated Sicilian males from nine different towns on the main island and from the island of Pantelleria. (c) 2005 Elsevier Ireland Ltd. All rights reserved.

GeneticshaplotypeChromosomes Human YPopulation sampleshort tandem repeatHaplotypePopulation geneticsY-chromosome; Short tandem repeats; Haplotype; SicilyBiologyY chromosomeDNA Fingerprintinglanguage.human_languageWhite PeoplePathology and Forensic MedicineGenetics PopulationShort tandem repeatsHaplotypesTandem Repeat SequenceslanguageMicrosatelliteHumansLawSicilianY-chromosomeSicily
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Compatibility of Rhizobial Genotypes within Natural Populations of Rhizobium leguminosarum Biovar viciae for Nodulation of Host Legumes

2003

ABSTRACT Populations of Rhizobium leguminosarum biovar viciae were sampled from two bulk soils, rhizosphere, and nodules of host legumes, fava bean ( Vicia faba ) and pea ( Pisum sativum ) grown in the same soils. Additional populations nodulating peas, fava beans, and vetches ( Vicia sativa ) grown in other soils and fava bean-nodulating strains from various geographic sites were also analyzed. The rhizobia were characterized by repetitive extragenomic palindromic-PCR fingerprinting and/or PCR-restriction fragment length polymorphism (RFLP) of 16S-23S ribosomal DNA intergenic spacers as markers of the genomic background and PCR-RFLP of a nodulation gene region, nodD , as a marker of the sy…

GenotypeBulk soilBiologymedicine.disease_causeApplied Microbiology and BiotechnologyPlant RootsPolymerase Chain ReactionRhizobium leguminosarumRhizobiaPlant MicrobiologySymbiosisBacterial ProteinsNitrogen FixationBotanyGenotypemedicineSymbiosisSoil Microbiology[SDV.EE]Life Sciences [q-bio]/Ecology environmentRhizosphereRhizobium leguminosarumEcologyPeasfood and beveragesbiology.organism_classificationDNA FingerprintingVicia fabaVicia faba[SDV.EE] Life Sciences [q-bio]/Ecology environmentNitrogen fixationFood ScienceBiotechnologyPlasmids
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High-resolution genotyping of Campylobacter strains isolated from poultry and humans with amplified fragment length polymorphism fingerprinting.

1999

ABSTRACT For epidemiological studies of Campylobacter infections, molecular typing methods that can differentiate campylobacters at the strain level are needed. In this study we used a recently developed genotyping method, amplified fragment length polymorphism (AFLP), which is based on selective amplification of restriction fragments of chromosomal DNA, for genetic typing of Campylobacter jejuni and Campylobacter coli strains derived from humans and poultry. We developed an automated AFLP fingerprinting method in which restriction endonucleases Hin dIII and Hha I were used in combination with one set of selective PCR primers. This method resulted in evenly distributed band patterns for amp…

GenotypeGenetics and Molecular BiologyCampylobacter coliDeoxyribonuclease HindIIImedicine.disease_causeApplied Microbiology and BiotechnologyCampylobacter jejuniPolymerase Chain ReactionPoultryMicrobiologyRestriction fragmentCampylobacter jejuniGenotypeCampylobacter InfectionsmedicineAnimalsDeoxyribonucleases Type II Site-SpecificGenotypingDNA PrimersGeneticsEcologybiologyCampylobacterfood and beveragesReproducibility of ResultsCampylobacterbiology.organism_classificationDNA FingerprintingBacterial Typing TechniquesElectrophoresis Gel Pulsed-FieldDNA profilingCampylobacter colibiology.proteinAmplified fragment length polymorphismFood ScienceBiotechnologyApplied and environmental microbiology
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Evaluation of genotypic and phenotypic methods to distinguish clinical from environmental Vibrio vulnificus strains.

2009

ABSTRACT Vibrio vulnificus is a heterogeneous bacterial species that comprises virulent and avirulent strains from environmental and clinical sources that have been grouped into three biotypes. To validate the typing methods proposed to distinguish clinical from environmental isolates, we performed phenotypic (API 20E, API 20NE, and BIOLOG tests) and genetic (ribotyping and DNA polymorphism at several loci) studies with a large strain collection representing different biotypes, origins, and host ranges. No phenotypic method was useful for biotyping or grouping strains with regard to the origin of an isolate, and only the BIOLOG system was reliable for identifying the strains at the species …

GenotypePopulationVibrio vulnificusPublic Health MicrobiologyApplied Microbiology and BiotechnologyMicrobiologyRibotypingGenotypeEnvironmental MicrobiologyCluster AnalysisHumansTypingeducationGenotypingVibrio vulnificusGeneticseducation.field_of_studyPolymorphism GeneticEcologybiologybiology.organism_classification16S ribosomal RNADNA FingerprintingBacterial Typing TechniquesDNA profilingVibrio InfectionsBacteris patògensFood ScienceBiotechnology
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HPTLC Phenolic Profiles as Useful Tools for the Authentication of Honey

2018

The present study reveals the utility of high-performance thin-layer chromatographic (HPTLC) fingerprinting of phenolic constituents for the authentication of monofloral honeys. The obtained data enables a more complete assessment of honey quality and the identification of emerging threats to honey quality. The developed procedure facilitates differentiation of varietal honeys and detection of honey adulterations. We used an HPTLC fingerprint analysis to determine the characteristic patterns of different honey types (willow, buckwheat, heather, pine honeydew, and manuka honey). The HPTLC chromatograms were used to determine the differences in the botanical origin of the honey samples on the…

HPTLC fingerprintHplc analysisHoneydewChromatographyHptlc fingerprintChemistry010401 analytical chemistryhoneyphenolic compounds04 agricultural and veterinary sciences040401 food science01 natural sciencesApplied Microbiology and BiotechnologyHoney samplesManuka Honey0104 chemical sciencesAnalytical Chemistry0404 agricultural biotechnologyhigh-performance thin-layer chromatographySafety Risk Reliability and QualitySafety ResearchFood ScienceFood Analytical Methods
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Evolution of tissue-specific keratins as deduced from novel cDNA sequences of the lungfish Protopterus aethiopicus.

2005

Lungfishes are possibly the closest extant relatives of the land vertebrates (tetrapods). We report here the cDNA and predicted amino acid sequences of 13 different keratins (ten type I and three type II) of the lungfish Protopterus aethiopicus. These keratins include the orthologs of human K8 and K18. The lungfish keratins were also identified in tissue extracts using two-dimensional polyacrylamide gel electrophoresis, keratin blot binding assays and immunoblotting. The identified keratin spots were analyzed by peptide mass fingerprinting which assigned seven sequences (inclusively Protopterus K8 and K18) to their respective protein spot. The peptide mass fingerprints also revealed the fac…

HistologyDNA ComplementaryMolecular Sequence DataFluorescent Antibody Techniquemacromolecular substancesPeptide MappingPathology and Forensic MedicineEvolution MolecularPeptide mass fingerprintingComplementary DNAKeratinAnimalsElectrophoresis Gel Two-DimensionalAmino Acid SequencePolyacrylamide gel electrophoresisLungfishchemistry.chemical_classificationProtopterusintegumentary systembiologyPhylogenetic treeLampreyFishesCell BiologyGeneral MedicineAnatomybiology.organism_classificationchemistryEvolutionary biologySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationKeratinsEuropean journal of cell biology
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Response of soil bacterial community structure to successive perturbations of different types and intensities

2008

SummaryIn soil, genetic structure modifications of indigenousbacterial community consecutively to a severe stress(mercury contamination) were delayed when thecommunity was pre-exposed to various minor per-turbations (heat, copper and atrazine). Such minorperturbations induced transitory community struc-ture modifications leading to an increase of commu-nity stability towards a severe mercury stress. Theseresults illustrated well the short-term pre-adaptationprocess for bacterial community hypothesizing thatcommunity submitted to perturbations become moreresistant to withstand another stress. Compared with other environmental matrices of the bio-sphere, soils are considered as the main reservo…

Hot TemperatureRELATION SOL MICROORGANISME010501 environmental sciencesBiology01 natural sciencesMicrobiology03 medical and health sciencesMetals HeavyMercury contaminationEcosystemSoil MicrobiologyEcology Evolution Behavior and Systematics030304 developmental biology0105 earth and related environmental sciences2. Zero hunger0303 health sciencesMicrobial ViabilityHerbicidesEcologyCommunity structureMercury15. Life on landDNA FingerprintingSoil quality[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyMicrobial population biology13. Climate actionSoil waterAtrazineCopper
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