نتایج جستجو برای: Q PCR

تعداد نتایج: 295197  

Journal: :FEMS microbiology ecology 2009
Cindy J Smith A Mark Osborn

Quantitative PCR (Q-PCR or real-time PCR) approaches are now widely applied in microbial ecology to quantify the abundance and expression of taxonomic and functional gene markers within the environment. Q-PCR-based analyses combine 'traditional' end-point detection PCR with fluorescent detection technologies to record the accumulation of amplicons in 'real time' during each cycle of the PCR amp...

Journal: :Journal of clinical microbiology 2008
Hyong Sun Kim Dong-Min Kim Ganesh Prasad Neupane Yu-mi Lee Nam-Woong Yang Sook Jin Jang Sook-In Jung Kyung-Hwa Park Hae-Ryoung Park Chang Seop Lee Sun Hee Lee

We conducted a prospective study to target toxR in the blood of patients with skin and soft tissue infections who were admitted to four tertiary hospitals to assess the clinical usefulness of real-time quantitative PCR (Q-PCR) as a diagnostic technique. We performed conventional PCR (C-PCR), nested PCR (N-PCR), and Q-PCR assays and compared the results to those obtained using the "gold standard...

Journal: :journal of plant molecular breeding 2015
abbas hajipour mohammad-mehdi sohani valiollah babaeizad hasan hasani-kumleh

the root endophytic fungus, piriformospora indica, colonizes roots of a large number of plant species including cereals and brasicaceae. there are several reports indicating that p. indica protects roots from different path-ogens. in the present study, rice plants were pre-inoculated with p. indica and were subsequently infected with fusarium proliferatum, as the causal agent of root rot and cr...

2016
Enrico Tatti Boyd A. McKew Corrine Whitby Cindy J. Smith

Real Time Polymerase Chain Reaction also known as quantitative PCR (q-PCR) is a widely used tool in microbial ecology to quantify gene abundances of taxonomic and functional groups in environmental samples. Used in combination with a reverse transcriptase reaction (RT-q-PCR), it can also be employed to quantify gene transcripts. q-PCR makes use of highly sensitive fluorescent detection chemistr...

Journal: :Saudi medical journal 2007
Selma Gokahmetoglu Esma Deniz

OBJECTIVE To compare the real-time (RT), and qualitative (Q) polymerase chain reaction (PCR) assays for detection of Cytomegalovirus (CMV) DNA. METHODS The study took place in the Department of Microbiology, Erciyes University, Kayseri, and in Iontek Laboratory, Istanbul, Turkey, from August to December 2006. One hundred and seven clinical specimens from 67 patients were included in the study...

2009
Vassiliki Kotoula Elpida Charalambous Bart Biesmans Andigoni Malousi Eleni Vrettou George Fountzilas George Karkavelas

BACKGROUND Testing for tumor specific mutations on routine formalin-fixed paraffin-embedded (FFPE) tissues may predict response to treatment in Medical Oncology and has already entered diagnostics, with KRAS mutation assessment as a paradigm. The highly sensitive real time PCR (Q-PCR) methods developed for this purpose are usually standardized under optimal template conditions. In routine diagn...

Journal: :Journal of clinical microbiology 2008
Musa Hindiyeh Gill Smollen Zehava Grossman Daniela Ram Yehudit Davidson Fernando Mileguir Marina Vax Debbie Ben David Ilana Tal Galia Rahav Ari Shamiss Ella Mendelson Nathan Keller

Carbapenem resistance among Enterobacteriaceae is an emerging problem worldwide. Klebsiella pneumoniae carbapenemase (bla(KPC)) enzymes are among the most common beta-lactamases described. In this study, we report the development and validation of a real-time PCR (q-PCR) assay for the detection of bla(KPC) genes using TaqMan chemistry. The q-PCR amplification of bla(KPC) DNA was linear over 7 l...

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