Search results for "Amplicon"

showing 10 items of 53 documents

Borrelia miyamotoi is widespread in Ixodes ricinus ticks in southern Norway.

2015

From April to October 2007, host-seeking Ixodes ricinus ticks were collected from four locations in southern Norway; Farsund, Mandal, Sogne and Tromoy, respectively. Larvae (n=210), nymphs (n=1130) and adults (n=449) were investigated for infection with Borrelia miyamotoi by real-time polymerase chain reaction (PCR) amplification of part of the 16S rRNA gene. Results were verified by direct sequencing of the PCR amplicon generated from the rrs (16S)-rrl (23S) intergenetic spacer. B. miyamotoi was detected at all sites and throughout the period of questing activity, with infection prevalence (≤1.26%) similar to what has been seen in other European countries. Detection of the relapsing fever …

DNA BacterialMaleNymphIxodes ricinusrelapsing feverMolecular Sequence DataZoologyBorrelia miyamotoiMicrobiologylaw.inventionlawmedicineAnimalsNymphPathogenPolymerase chain reactionPhylogenybiologyIxodesNorwayBorreliaAmpliconbiology.organism_classification16S ribosomal RNAmedicine.diseaseVirologyInfectious DiseasesInsect ScienceParasitologyFemaleTicks and tick-borne diseases
researchProduct

A real-time PCR assay for detection and quantification of 2-branched (1,3)-β-D–glucan producing lactic acid bacteria in cider

2010

28 p.-1 fig.-4 tab.

DNA Bacterialbeta-GlucansFood spoilageMicrobiologyMelting curve analysisMicrobiologyPolysaccharidesLactobacillus(13)(12)--D-glucanLactic acid bacteriaFood sciencePediococcusOenococcusOenococcus oeniDNA PrimersbiologyBacteriaSpoilageReverse Transcriptase Polymerase Chain ReactionAlcoholic BeveragesGeneral MedicineAmpliconbiology.organism_classificationBacterial Typing TechniquesLactobacillusCidersGenes BacterialGlucosyltransferasesFood MicrobiologyPediococcusProteoglycansOenococcusBacteriaFood ScienceReal-time PCR
researchProduct

Molecular tools to assess the diversity and density of denitrifying bacteria in their habitats

2007

Publisher Summary This chapter describes the molecular tools to assess the diversity and density of denitrifying bacteria in their habitats. Genome sequencing and metagenomic projects might even provide new denitrification gene sequences, which could aid in designing more broad range primers. Most information is obtained by cloning and sequencing the polymerase chain reaction (PCR) amplicons, but a more rapid analysis is achieved using fingerprinting techniques. As all PCR-based analyses, the fingerprinting techniques are subjected to well-known biases introduced by, e.g., DNA extraction procedures, primer selection, and PCR conditions. For denitrifiers, the PCR-RFLP (restriction fragment l…

EcologydenitrifiersComputational biologyAmpliconBiologydggeDNA extraction[SDE.ES]Environmental Sciences/Environmental and SocietyDNA sequencing[SDE.BE] Environmental Sciences/Biodiversity and EcologyDenitrifying bacteriaTerminal restriction fragment length polymorphismMetagenomics[SDE.ES] Environmental Sciences/Environmental and SocietyRestriction fragment length polymorphism[SDE.BE]Environmental Sciences/Biodiversity and EcologyTemperature gradient gel electrophoresis
researchProduct

Helminth Microbiota Profiling Using Bacterial 16S rRNA Gene Amplicon Sequencing: From Sampling to Sequence Data Mining

2021

Symbiont microbial communities play important roles in animal biology and are thus considered integral components of metazoan organisms, including parasitic worms (helminths). Nevertheless, the study of helminth microbiomes has thus far been largely overlooked, and symbiotic relationships between helminths and their microbiomes have been only investigated in selected parasitic worms. Over the past decade, advances in next-generation sequencing technologies, coupled with their increased affordability, have spurred investigations of helminth-associated microbial communities aiming at enhancing current understanding of their fundamental biology and physiology, as well as of host-microbe intera…

FOS: Computer and information sciencesBioinformaticsComputational biologyBiologyDNA sequencingSymbiosisHelminthsRNA Ribosomal 16Sparasitic diseasesHelminthAnimalsData MiningHelminthsMicrobiomeGeneBacterial 16S rRNA geneIndirect life cycleHigh-throughput sequencingMicrobiotaHigh-Throughput Nucleotide SequencingGenes rRNASchistosoma mansoniAmplicon sequencingHuman genomeSample collectionWorm-associated microbiome
researchProduct

Analysis of artificially degraded DNA using STRs and SNPs—results of a collaborative European (EDNAP) exercise

2005

Recently, there has been much debate about what kinds of genetic markers should be implemented as new core loci that constitute national DNA databases. The choices lie between conventional STRs, ranging in size from 100 to 450 bp; mini-STRs, with amplicon sizes less than 200 bp; and single nucleotide polymorphisms (SNPs). There is general agreement by the European DNA Profiling Group (EDNAP) and the European Network of Forensic Science Institutes (ENFSI) that the reason to implement new markers is to increase the chance of amplifying highly degraded DNA rather than to increase the discriminating power of the current techniques. A collaborative study between nine European and US laboratories…

Forensic GeneticsGeneticsAnalysis of VarianceGenotypeDNA Degradation NecroticSingle-nucleotide polymorphismAmpliconBiologyDNA FingerprintingPolymerase Chain ReactionPolymorphism Single NucleotidePathology and Forensic MedicineEuropeBloodDNA profilingTandem Repeat SequencesGenetic markerHumansMicrosatelliteMultiplexDegraded dnaMini strsSalivaLawForensic Science International
researchProduct

Rapid PCR-based test for identifying Candida albicans by using primers derived from the pH-regulated KER1 gene.

2006

A PCR-based method in combination with a simple, reliable and inexpensive DNA extraction procedure for rapid detection of Candida albicans clinical isolates is described here. The extraction protocol is based on a combination of chemical (NaOH and detergents) and physical (boiling) treatments, thus avoiding many of the problems inherent in the currently available DNA extraction protocols (basically the use of expensive and/or toxic chemical reagents), and may be useful for daily clinical routine. The PCR-based system described here uses a single pair of primers (SC1F and SC1R) deduced from the C. albicans-specific KER1 gene sequence. These primers amplify a 670-bp fragment of the KER1 gene.…

Fungal proteinbiologyInverse polymerase chain reactionLysineGenes FungalMultiple displacement amplificationGlutamic AcidMembrane ProteinsGeneral MedicineAmpliconHydrogen-Ion Concentrationbiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologyDNA extractionMolecular biologyPolymerase Chain ReactionCorpus albicanslaw.inventionFungal ProteinslawCandida albicansCandida albicansPolymerase chain reactionDNA PrimersFEMS yeast research
researchProduct

Identification of pathogenic yeast species by polymerase chain reaction amplification of the RPS0 gene intron fragment.

2009

Aims: This work focuses on the development of a method for the identification of pathogenic yeast. With this aim, we target the nucleotide sequence of the RPS0 gene of pathogenic yeast species with specific PCR primers. PCR analysis was performed with both the genomic DNA, whole cells of clinical isolates of Candida species and clinical samples. Methods and Results: A single pairs of primers, deduced from the nucleotide sequence of the RPS0 gene from pathogenic yeast, were used in PCR analysis performed with both the genomic DNA and whole cells of clinical isolates of Candida species and clinical samples. The primers designed are highly specific for their respective species and produce ampl…

Genes FungalMolecular Sequence DataBiologyApplied Microbiology and BiotechnologyPolymerase Chain ReactionSensitivity and Specificitylaw.inventionchemistry.chemical_compoundSpecies SpecificitylawHumansAmino Acid SequenceDNA FungalGenePolymerase chain reactionCandidaDNA PrimersGeneticsIntronNucleic acid sequenceGeneral MedicineAmpliconYeastIntronsgenomic DNAchemistryDNABiotechnologyJournal of applied microbiology
researchProduct

Development of a new multiplex assay for STR typing of telogen hair roots

2006

Abstract We have developed a new strategy in which 10 STR systems plus amelogenin were simultaneously amplified from telogen hair roots with maximal fragment sizes smaller than 270 base pairs. The multiplex includes six STR loci from the European standard set of loci (ESS) for DNA databases (D3S1358, D8S1179, D21S11, THO1, FGA and VWA) as well as four additional STR systems selected for their robustness and short amplicon sizes (D2S1338, D12S391, TPOX and D5S818). Due to the biotinylation of the reverse primers from five STRs systems, these PCR products can be separated from the other six amplicons after PCR amplification. The two sub-multiplexes were then analyzed in two different runs on …

GeneticsBase pairSTR multiplex systemGeneral MedicineBiologyAmpliconMolecular biologylaw.inventionCapillary electrophoresisSTR analysislawMultiplexAmelogeninPolymerase chain reactionInternational Congress Series
researchProduct

Intragenic anaplastic lymphoma kinase (ALK) rearrangements: Translocations as a novel mechanism ofALKactivation in neuroblastoma tumors

2014

Anaplastic lymphoma kinase (ALK) has been demonstrated to be deregulated in sporadic as well as in familiar cases of neuroblastoma (NB). Whereas ALK-fusion proteins are common in lymphoma and lung cancer, there are few reports of ALK rearrangements in NB indicating that ALK mainly exerts its oncogenic capacity via activating mutations and/or overexpression in this tumor type. In this study, 332 NB tumors and 13 cell lines were screened by high resolution single nucleotide polymorphism microarray. Gain of 2p was detected in 23% (60/332) of primary tumors and 46% (6/13) of cell lines, while breakpoints at the ALK locus were detected in four primary tumors and two cell lines. These were furthe…

GeneticsCancer ResearchKinaseGene rearrangementAmpliconBiologymedicine.diseasemedicine.disease_causeLymphomaExonhemic and lymphatic diseasesNeuroblastomaGeneticsmedicineCancer researchAnaplastic lymphoma kinaseCarcinogenesisGenes, Chromosomes and Cancer
researchProduct

Validation and casework testing of the BioPlex-11 for STR typing of telogen hair roots.

2005

A new STR typing strategy has been developed allowing the simultaneous amplification and subsequent analysis of 11 polymorphic systems with amplicon sizes smaller than 270 bp. The multiplex amplification reaction includes six STR loci from the European standard set of loci (ESS) for DNA databases (D3S1358, D8S1179, D21S11, THO1, FGA and VWA) as well as four additional STR systems selected for their robustness (D2S1338, D12S391, TPOX and D5S818) together with the sex-specific locus amelogenin. After PCR amplification, the multiplex reaction is splitted into two sets of STR multiplexes by using biotin labelled primers only for one set. Using streptavidin-coated Sepharose beads five STR system…

GeneticsHeterozygoteAmelogeninSTR multiplex systemElectrophoresis CapillaryLocus (genetics)BiologyAmpliconDNA FingerprintingPolymerase Chain ReactionPathology and Forensic Medicinelaw.inventionDental Enamel ProteinslawTandem Repeat SequencesMicrosatelliteHumansMultiplexTypingAmelogeninLawHair FolliclePolymerase chain reactionForensic science international
researchProduct