Search results for "probe"

showing 10 items of 534 documents

Molecular diversity at the self-incompatibility locus is a salient feature in natural populations of wild tomato (Lycopersicon peruvianum)

1993

A cDNA encoding a stylar protein was cloned from flowers of self-incompatible wild tomato (Lycopersicon peruvianum). The corresponding gene was mapped to the S locus, which is responsible for self-incompatibility. The nucleotide sequence was determined for this allele, and compared to other S-related sequences in the Solanaceae. The S allele was used to probe DNA from 92 plants comprising 10 natural populations of Lycopersicon peruvianum. Hybridization was conducted under moderate and permissive stringencies in order to detect homologous sequences. Few alleles were detected, even under permissive conditions, underscoring the great sequence diversity at this locus. Those alleles that were de…

GeneticsBase SequencebiologyMolecular Sequence DataNucleic acid sequenceChromosome MappingGenetic Variationfood and beveragesLocus (genetics)Sequence alignmentPlantsGenes Plantbiology.organism_classificationLycopersiconBlotting SouthernComplementary DNAGeneticsWild tomatoAmino Acid SequenceCloning MolecularAlleleDNA ProbesMolecular BiologyGeneAllelesMolecular and General Genetics MGG
researchProduct

Analysis of extended genomic rearrangements in oncological research.

2007

Screening for genomic rearrangements is a fundamental task in the genetic diagnosis of many inherited disorders including cancer-predisposing syndromes. Several methods were developed for analysis of structural genomic abnormalities, some are targeted to the analysis of one or few specific loci, others are designed to scan the whole genome. Locus-specific methods are used when the candidate loci responsible for the specific pathological condition are known. Whole-genome methods are used to discover loci bearing structural abnormalities when the disease-associated locus is unknown. Three main approaches have been employed for the analysis of locus-specific structural changes. The first two a…

GeneticsChromosome AberrationsGene RearrangementRecombination GeneticHybridization probecopy number gene dosage locus-specific molecular diagnosis mutation detection structural variationsGenomicsHematologyGene rearrangementGenomicsBiologyMolecular Inversion ProbeMedical OncologyOncologyNeoplasmsMultiplex polymerase chain reactionHumansMultiplexGenotypingSNP arrayAnnals of oncology : official journal of the European Society for Medical Oncology
researchProduct

Genetic analysis of heat shock response in three Drosophila species of the obscura group

1992

Heat shock response was investigated in three species of the obscura group of the Drosophila genus (D. subobscura, D. guanche, and D. madeirensis) by chromosome cytology analysis and [3H]uridine labeling. A set of eight puffs (2C, 15DE, 18C, 27A, 31CD, 85AB, 89A, and 94A) were induced after heat treatments in each of the three species; 18C, 27A, 89A, and 94A were the most heavily labeled in the autoradiograms after the induced conditions. From the in situ results using the major heat shock genes of D. melanogaster as a probe, it was inferred that the 18C, 94A, 89A, and 27A loci of the three obscura group species are homologous to D. melanogaster loci, which contain, HSP82, HSP70, HSP68, an…

GeneticsHot TemperaturePolytene chromosomebiologyGeneral Medicinebiology.organism_classificationBiological EvolutionChromosomesDrosophila subobscuraChromosome BandingHsp70Drosophila melanogasterMolecular ProbesHeat shock proteinDrosophilidaeGeneticsMelanogasterAnimalsDrosophilaDrosophila (subgenus)Heat shockMolecular BiologyHeat-Shock ProteinsBiotechnologyGenome
researchProduct

Forensics of birds of prey by DNA fingerprinting with 32P-labeled oligonucleotide probes.

1991

Paternity tests on confiscated families of eight species of birds of prey were carried out successfully by DNA fingerprinting with 32P-labeled oligonucleotide probes. Variations in the number of hybridized fragments, depending on the species of birds, are observed using the same probe, as well as differences of polymorphism by hybridizing the DNA samples with several oligonucleotide probes.

GeneticsMaleBase CompositionBase SequenceOligonucleotideClinical BiochemistryPhosphorus IsotopesBiologyBiochemistryDNA FingerprintingAnalytical ChemistryPredationBirdschemistry.chemical_compoundchemistryDNA profilingPolymorphism (computer science)Paternity testsAnimalsBase sequenceMolecular probeOligonucleotide ProbesDNAPolymorphism Restriction Fragment LengthRepetitive Sequences Nucleic AcidElectrophoresis
researchProduct

Biostatistical basis of individualization and segregation analysis using the multilocus DNA probe MZ 1.3: results of a collaborative study.

1992

A collaborative study using the multilocus minisatellite DNA probe MZ 1.3 was carried out to investigate segregation information, mutation rate, DNA fragment frequencies as well as band sharing characteristics. The fingerprint patterns of 393 children as well as 694 unrelated individuals were analysed after digestion of DNA with the restriction enzyme HinfI. A mutation rate of 1% per meiosis or 0.04% per band was found with a mean number of 26 bands/individual. It was shown that maternal and paternal fragments are inherited in equal proportions. Population frequencies of restriction fragments demonstrated a distribution with increasing frequencies in the small fragment size range below 10 k…

GeneticsMaleMutation rateeducation.field_of_studyBiometrybiologyHybridization probePopulationPaternityDNA FingerprintingPathology and Forensic MedicineRestriction fragmentRestriction enzymeMinisatelliteDNA profilingData Interpretation Statisticalbiology.proteinHumansFemaleeducationMolecular probeChildDNA ProbesLawProbabilityForensic science international
researchProduct

Paternity Analysis Using the Multilocus DNA Probe MZ 1.3

1992

The multilocus minisatellite DNA probe MZ 1.3 detects hypervariable restriction fragment patterns in genomic DNA of man and animals. It can be used for segregation analysis in cases of disputed paternity (Schacker et al., 1991; Rittner et al., 1991a), for identification purposes in forensic medicine and stain analysis (Ogata et al., 1990; Rittner et al., 1991b), as well as in animal breeding for pedigree analysis and verification of inbred strains (Hins & Gruber, 1991). Hypervariable fragment patterns can be generated by using frequently cutting restriction enzymes, e.g. Hinf I, Hae Ill, Msp I, Mbo I, and Rsa I. A non-radioactive system using the digoxigenin antidigoxigenin system may be us…

GeneticsRestriction enzymechemistry.chemical_compoundgenomic DNAMinisatellitechemistryInbred strainHybridization probebiology.proteinDigoxigeninBiologyDNARestriction fragment
researchProduct

Mixture analysis using SWaP™ SNPs and non-biallelic SNPs

2006

Abstract Improved analysis of degraded samples, increased throughput, and a wider choice of typing platforms are some of the significant advantages offered by single nucleotide polymorphism (SNP) genotyping over established short tandem repeat (STR)-based systems. However, DNA mixtures present a considerable problem to SNP analysis as there is currently no generally accepted technique that allows recognition of the presence of a mixed profile or identification of the individual contributors. We present the first demonstration of SNP mixture analysis with an approach based upon the use of two rare subsets of SNPs: SWaP™ SNPs and non-biallelic SNPs and discuss their value for forensic mixture…

GeneticsSNPMicrosatelliteSingle-nucleotide polymorphismGeneral MedicineTag SNPBiologyMolecular Inversion ProbeGenotypingSNP arraySNP genotypingInternational Congress Series
researchProduct

Microduplications At 22q11.21 are Associated with Classic Bladder Exstrophy

2010

Purpose Classic exstrophy of the bladder (CBE) is part of the exstrophy-epispadias complex (EEC), a spectrum of urogenital anomalies in which part or all of the distal urinary tract fails to close. Familial occurrence has been observed, and previous studies have suggested an underlying multifactorial mode of inheritance. To date, no causative genetic or non-genetic factor has been unequivocally identified in humans. The present study aimed to identify microaberrations characterized by loss or gain of genomic material that contribute to the EEC at a genome-wide level. Material and Methods Molecular karyotyping, utilizing 549,839 single nucleotide polymorphisms (SNPs) with an average spacing …

Geneticsbusiness.industryUrologySingle-nucleotide polymorphismKaryotypemedicine.diseasePenetranceBladder exstrophyDiGeorge syndromePediatrics Perinatology and Child HealthGene duplicationChromosomal regionMedicineMultiplex ligation-dependent probe amplificationbusinessJournal of Pediatric Urology
researchProduct

PCR-Typing of the Human HLA-DQα Locus: Population Genetics and Application in Forensic Casework

1991

Multi- and single-locus probes recognizing highly polymorphic DNA sequences throughout the genome ([1–3]; C. Rittner, this volume) have become powerful tools for paternity testing and forensic stain analysis. In forensic casework, however, DNA probe technology can often not be applied, since genomic DNA extracted from stain material exposed to conditions of high temperatures and humidity is degraded. Also, the amount of DNA to be typed may not be sufficient to use DNA probe technology, e.g. if extracted from minute blood or sperm stains, from single hairs or from cell smears on microscope slides.

Geneticsgenomic DNAchemistry.chemical_compoundchemistryHybridization probePopulation geneticsLocus (genetics)BiologyGenomeStainDNA sequencingDNA
researchProduct

Centromeric enrichment of LINE-1 retrotransposon in two species of South American monkeys Alouatta belzebul and Ateles nancymaae (Platyrrhini, Primat…

2022

LINE-1 sequences have been linked to genome evolution, plasticity and speciation; however, despite their importance, their chromosomal distribution is poorly known in primates. In this perspective, we used fluorescence in situ hybridization (FISH) to map LINE-1 probes onto two representative platyrrhine species, Aotus nancymaae (Cebidae) and Alouatta belzebul (Atelidae), both characterized with highly rearranged karyotypes, in order to investigate their chromosomal distribution and role and to better characterize the two genomes. We found centromeric enrichment of LINE-1 sequences on all biarmed and acrocentric chromosomes co-localized with heterochromatin C-positive bands. This distributio…

Geneticstransposable elements C-banding molecular cytogenetics probes genome evolutionSettore BIO/08 - AntropologiaGeneral Agricultural and Biological SciencesCaryologia
researchProduct