نتایج جستجو برای: taqman real time pcr

تعداد نتایج: 2269818  

Journal: :jundishapur journal of microbiology 0
nader divan khosroshahi cellular and molecular research centre, qazvin university of medical sciences, qazvin, ir iran taghi naserpour farivar cellular and molecular research centre, qazvin university of medical sciences, qazvin, ir iran; cellular and molecular research centre, qazvin university of medical sciences, qazvin, ir iran. tel: +98-9128801401, fax: +98-2833324971. pouran johari cellular and molecular research centre, qazvin university of medical sciences, qazvin, ir iran

background legionellaceae contains legionella genus with over 52 species and 64 serogroups. it is one of the most important causes of respiratory disease in human. more than 30% of hospital-acquired pneumonia is caused by legionella. ventilator-associated pneumonia (vap) is an infection acquired in hospital wards, particularly in intensive care unit (icu). this disease approximately affects 9% ...

Journal: :Journal of clinical microbiology 2011
Salome Troxler Ana Marek Irina Prokofieva Ivana Bilic Michael Hess

Avian hepatitis E virus (HEV) isolates could be separated into at least three genotypes. In this study, the development of the first duplex TaqMan real-time reverse transcription-PCR (RT-PCR) assay for detection and quantification of avian HEV is presented. Primers and probes binding within relatively conserved open reading frame 3 (ORF3) were designed. Tenfold dilution series of in vitro-trans...

2016
Zhanmin Liu Luxi Zhang Cuiyun Yang Xueying Xia

Maize chlorotic mottle virus (MCMV) infects maize plants and causes significant losses in corn production worldwide. In this study, a real-time TaqMan RTPCR assay for efficient detection of MCMV was described. A pair of primers amplifying a 131-bp DNA fragment and a TaqMan probe was designed targeting the novel molecular marker based on MCMV genome analysis sequences. The assay designed was hig...

2015
Sara A Bickersmith William Lainhart Marta Moreno Virginia M Chu Joseph M Vinetz Jan E Conn

We describe a simple method for detection of Plasmodium vivax and Plasmodium falciparum infection in anophelines using a triplex TaqMan real-time polymerase chain reaction (PCR) assay (18S rRNA). We tested the assay on Anopheles darlingi and Anopheles stephensi colony mosquitoes fed with Plasmodium-infected blood meals and in duplicate on field collected An. darlingi. We compared the real-time ...

Journal: :iranian journal of microbiology 0
b nomanpour department of microbiology, school of medicine, tehran university of medical sciences, tehran, iran. a ghodousi department of microbiology, school of medicine, tehran university of medical sciences, tehran, iran. a babaei department of anesthesiology, shaheed rajaei cardiovascular, medical & research center, vali- asr avenue tehran- iran. hr abtahi department of internal medicine, school of medicine, tehran university of medical sciences, tehran, iran. m tabrizi department of medical genetics, school of medicine, tehran university of medical sciences, tehran, iran. m feizabadi department of microbiology, school of medicine, tehran university of medical sciences, tehran, iran and 5pediatric infection diseas research center, tehran, university of medical science, tehran, iran.

background and objectives: pneumonia with acinetobacter baumannii has a major therapeutic problem in health care settings. decision to initiate correct antibiotic therapy requires rapid identification and quantification of organism. the aim of this study was to develop a rapid and sensitive method for direct detection of a. baumannii from respiratory specimens. materials and methods : a taqman ...

Journal: :Journal of clinical microbiology 2002
Monique Nijhuis Noortje van Maarseveen Rob Schuurman Sandra Verkuijlen Machiel de Vos Karin Hendriksen Anton M van Loon

We developed a rapid and sensitive method for the routine detection of all members of the enterovirus genus in different clinical specimens by using real-time TaqMan quantitative PCR. Multiple primer and probe sets were selected in the highly conserved 5'-untranslated region of the enterovirus genome. Our assay detected all 60 different enterovirus species tested, whereas no reactivity was obse...

Journal: :Clinical chemistry 2009
Jin Li Lilin Wang Pasi A Jänne G Mike Makrigiorgos

BACKGROUND DNA genotyping with mutation-specific TaqMan(R) probes (Applied Biosystems) is broadly used in detection of single-nucleotide polymorphisms but is less so for somatic mutations because of its limited selectivity for low-level mutations. We recently described coamplification at lower denaturation temperature-PCR (COLD-PCR), a method that amplifies minority alleles selectively from mix...

2016
Jeni Vuong Jean-Marc Collard Melissa J. Whaley Issaka Bassira Issaka Seidou Seydou Diarra Rasmata T. Ouédraogo Dinanibè Kambiré Thomas H. Taylor Claudio Sacchi Leonard W. Mayer Xin Wang Vishnu Chaturvedi

Neisseria meningitidis (Nm), Haemophilus influenzae (Hi), and Streptococcus pneumoniae (Sp) are the lead causes of bacterial meningitis. Detection of these pathogens from clinical specimens using traditional real-time PCR (rt-PCR) requires DNA extraction to remove the PCR inhibitors prior to testing, which is time consuming and labor intensive. In this study, five species-specific (Nm-sodC and ...

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