Search results for "TaqMan"

showing 10 items of 35 documents

Detection and quantification of Streptococcus pneumoniae from Iranian patients with pneumonia and individual carriers by real time PCR

2011

The aim of this study was to develop a real time polymerase chain reaction (PCR) for quantitative detection of Streptococcus pneumoniae from clinical respiratory specimens. Initially, 184 respiratory specimens from patients with community acquired pneumonia (CAP) (n = 129) and 55 cases with hospital associated pneumonia (HAP) were bacteriologically investigated. To check the colonization status among the healthy individuals, 32 preschool and 31 adults were screened in parallel. All specimens were cultured on selective culture media to isolate S. pneumoniae, Legionella spp. and Mycoplasma spp. A 166 bp fragment corresponding to cbp A gene of S. pneumoniae was amplified from clinical specimen…

Mycoplasma pneumoniaeSettore MED/07 - Microbiologia E Microbiologia ClinicabiologyLegionellaStreptococcus pneumoniae community acquired pneumonia (CAP) real time polymerase chain reaction (PCR) choline binding protein A (cbp AMycoplasmamedicine.disease_causemedicine.diseasebiology.organism_classificationApplied Microbiology and BiotechnologyVirologyrespiratory tract diseasesMicrobiologyPneumoniaCommunity-acquired pneumoniaStreptococcus pneumoniae community acquired pneumonia (CAP) real time polymerase chain reaction (PCR) choline binding protein A (cbp A).Chlamydophila pneumoniaeStreptococcus pneumoniaeGeneticsmedicineTaqManAgronomy and Crop ScienceMolecular BiologyBiotechnology
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Abstract 448: Molecular analysis of BRAF gene and PTEN gene expression in metastatic colorectal cancer patients: Feasibility study

2014

Abstract Introduction There are numerous causes triggering CRC. 25-80% of CRC shown a deregulation in Epidermal Growth Factor Receptor (EGFR) pathway. Two signaling pathways downstream of the EGFR are dysregulated in CRC the mitogen-activated protein kinase (MAPK) and the phosphoinositide-3-kinase (PI3K) pathway. Activating mutations in KRAS and BRAF (MAPK pathway) and PIK3CA affect prognosis and/or response to anti-EGFR MoAb. PTEN is a downstream effector of EGFR pathway and is involved in PI3K pathway. Loss of PTEN protein expression can occur through epigenetic silencing and mutation or allelic loss. Immunohistochemistry (IHC) is the most effective way to assay for loss of PTEN expressio…

Neuroblastoma RAS viral oncogene homologCancer ResearchPredictive markerbiologyColorectal cancerCancermedicine.diseasemedicine.disease_causeOncologyCancer researchTaqManmedicinebiology.proteinPTENKRASPI3K/AKT/mTOR pathwayCancer Research
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Simultaneous detection of the main black aspergilli responsible for ochratoxin A (OTA) contamination in grapes by multiplex real-time polymerase chai…

2009

9 pages.

Ochratoxin AAspergillus niger aggregateGrapesHealth Toxicology and MutagenesisFood ContaminationWineAspergillus carbonariusBiologyToxicologyPolymerase Chain ReactionSensitivity and SpecificityMelting curve analysisReal-time polymerase chain reactionlaw.inventionMicrobiology03 medical and health scienceschemistry.chemical_compoundSpecies SpecificitylawTaqManVitisDNA FungalOchratoxinPolymerase chain reaction030304 developmental biology2. Zero hunger0303 health sciencesMycotoxinChromatography030306 microbiologyPublic Health Environmental and Occupational HealthFungal geneticsOchratoxin AGeneral ChemistryGeneral MedicineMycotoxinsSpores FungalOchratoxins3. Good healthAspergillusReal-time polymerase chain reactionchemistrySpainCarcinogensSYBR Green IAspergillus tubingensisPolyketide synthaseFood Science
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Real-time PCR based procedures for detection and quantification of Aspergillus carbonarius in wine grapes

2008

9 pages, 4 tables, 1 figure.

Ochratoxin ATime FactorsFood ContaminationWineBiologyPolymerase Chain ReactionSensitivity and SpecificityMicrobiologyMicrobiologylaw.inventionchemistry.chemical_compoundSpecies SpecificitylawTaqManVitisDNA FungalOchratoxinPolymerase chain reactionDNA PrimersWineMycotoxinChromatographyGene Amplificationfood and beveragesOchratoxin AGeneral MedicineSpores FungalDNA extractiongenomic DNAAspergillusReal-time polymerase chain reactionchemistryConsumer Product SafetyPolyketide synthasePolyketide SynthasesWine grapesReal-time PCRFood ScienceInternational Journal of Food Microbiology
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Abstract A42: miR34a: A valuable indicator of differential outcome of Ewing sarcoma patients with complex functions

2014

Abstract The identification of reliable indicators of prognosis, which may allow the stratification of patients according to different risk at diagnosis isan important aspect of translational research in Ewing sarcoma (ES). In this paper, we validated our previous evidence showing how expression of miR34a in ES tumor samples at diagnosis was signficantly associated with tumor progression (Nakatani F. J Pathol 2012). Here we analyzed a different series of speciments derived from very controlled and homogeneously treated non-metastatic ES patients, and we compared evaluation of miR34a by RT-PCR using frozen samples with that obtained by in situ hybridization on paraffin-embedded samples . The…

OncologyCancer Researchmedicine.medical_specialtyPathologyProportional hazards modelbusiness.industryCancerIn situ hybridizationmedicine.diseasePediatric cancerOncologyTumor progressionMirna expressionInternal medicinemedicineTaqManSarcomabusinessCancer Research
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Prognostic Impact of Vegfa in Resectable Non-Small-Cell Lung Cancer

2014

ABSTRACT Aim: Angiogenesis is a main process which happens in tumors and that promotes its growth, invasive capacity and metastasis. Host genetic variability within VEGF pathway may affect angiogenic signaling and alter patient's sensitivity to anti-angiogenic therapies and therefore the prognostic. The goal in the present study is to analyze the prognostic value of several SNPs in angiogenic genes and the relative expression of those genes, using a cohort of patients diagnosed with resectable non-small cell lung cancer. Methods: This study included 127 resectable (I-IIIA) NSCLC patients. RNA and DNA extractions from tissues were performed using Trizol®. 20 ng of DNA were used for studies o…

Oncologymedicine.medical_specialtyPathologybusiness.industrySingle-nucleotide polymorphismHematologymedicine.diseaseMetastasisVascular endothelial growth factor AOncologyInternal medicineGenotypemedicineTaqManAdenocarcinomabusinessLung cancerSurvival analysisAnnals of Oncology
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Validation of microRNA expression profile in Oral Lichenoid Disease through cytological samples

2019

Background To validate oral exfoliative cytology in the analysis of the microRNA expression profile in Oral Lichenoid Disease (OLD).

Pathologymedicine.medical_specialtyDiseaseReal-Time Polymerase Chain Reaction03 medical and health sciences0302 clinical medicinemicroRNABiopsymedicineTaqManHumansOral mucosaGeneral DentistryOral Medicine and Pathologymedicine.diagnostic_testbusiness.industryGene Expression ProfilingResearch030206 dentistryMicroRNA Expression ProfileSmall interfering RNA:CIENCIAS MÉDICAS [UNESCO]Gene expression profilingMicroRNAsstomatognathic diseasesmedicine.anatomical_structureReal-time polymerase chain reactionOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASEpigeneticsSurgeryLichen planusbusinessMouth Diseases
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Quantification of PCR products by phosphate measurement

2008

Various techniques for quantification of PCR are available. Most frequently, the densitometric intensities of ethidium bromide-stained PCR products separated in gels are compared after normalizing to the levels of housekeeping gene products such as beta-actin. More precise, but extremely time consuming, is the technique of competitive PCR. Newer methods, such as tracking amplification in real-time, have high start-up and maintenance costs (e.g., TaqMan, Applied Biosystems; LightCycler, Roche; I-Cycler, Bio-Rad). Here, I describe an alternative, simple technique to quantify PCR products by determining the entire phosphate released during PCR. The method can be performed using common laborato…

Pcr cloningBiophysicsCell BiologyBiologyPolymerase Chain ReactionSensitivity and SpecificityBiochemistryPhosphate measurementCompetitive pcrPhosphatesHousekeeping geneMiceReal-time polymerase chain reactionBiochemistryEthidiumPrimer dimerGene expressionTaqManAnimalsMolecular BiologyCells CulturedDNA PrimersAnalytical Biochemistry
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Use of TaqMan® real-time PCR for rapid detection of Salmonella enterica serovar Typhi

2014

We evaluated the performances of a newly designed real-time polymerase chain reaction (PCR) assay using TaqMan® probes to detectSalmonellaTyphi. TaqMan® real-time PCR assays were performed by designed primers and probe based on thestaGgene for detectingS.Typhi. The specificity of the assay was evaluated on 15Salmonellaserovars. The analytical specificity was evaluated on 20 non-Salmonellamicroorganisms. The analytical sensitivity was assessed using decreasing DNA quantities ofS.Typhi ATCC 19430. Finally the detection capability of the TaqMan® real-time PCR assay on isolates recovered from patients withSalmonellainfections was compared to the conventional PCR assay. OnlyS.Typhi strain had po…

SerotypeSalmonellaSettore MED/07 - Microbiologia E Microbiologia ClinicaBiologySalmonella typhimedicine.disease_causeReal-Time Polymerase Chain ReactionSettore MED/42 - Igiene Generale E ApplicataRapid detectionSensitivity and Specificitylaw.inventionlawTaqManmedicineHumansTyphoid FeverPolymerase chain reactionreal time typhoid fever diagnosisDNA PrimersGeneral Immunology and MicrobiologyGeneral MedicineSalmonella typhiVirologyMolecular biologyBacterial Typing TechniquesReal-time polymerase chain reactionSalmonella enterica serovar TyphiGenes Bacterial
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Detection of Parietaria Mottle Virus by RT-qPCR: An Emerging Virus Native of Mediterranean Area That Undermine Tomato and Pepper Production in Southe…

2021

Parietaria mottle virus (PMoV) is considered an emerging virus in many countries of the Mediterranean basin, especially on tomato and pepper crops. Symptoms on tomato leaves and fruits can be easily confused with those induced by cucumber mosaic virus (CMV) with necrogenic satellite RNA (CMV-satRNA), tomato spotted wilt virus (TSWV) or tomato mosaic virus (ToMV). Mixed infection of these viruses has been also reported in some tomato cultivars, with an increase in the complexity of the symptoms and severity of the disease. Although a specific serum and riboprobes have been produced, nowadays no sensitive diagnostic methods are available for the rapid PMoV detection. Here, we have developed a…

emerging virusbiologyfungiRT-qPCRPlant culturefood and beveragesSettore AGR/12 - Patologia Vegetalefield surveyPlant Sciencebiology.organism_classificationemerging viruVirologyVirusSB1-1110Cucumber mosaic virusPMoV; RT-qPCR; early detection; emerging virus; field surveyPepperMethodsTaqManTomato mosaic virusSatellite (biology)CultivarPMoVearly detectionPathogen
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