نتایج جستجو برای: time qpcr

تعداد نتایج: 1899469  

Journal: :Arquivos brasileiros de oftalmologia 2017
Heloisa Nascimento Aripuanã Watanabe Ana Carolina Cabreira Vieira Andrea Pelegrini Maria Cecília Yu Paulo José Martins Bispo Celso Francisco Hernandes Granato Ana Luisa Höfling-Lima

Objective: Bacterial keratitis occurs worldwide, and despite recent developments, it remains a potentially blinding condition. This study assesses the presence of herpes simplex virus (HSV-1 and -2) and varicella zoster virus (VZV) by quantitative real-time polymerase chain reaction (qPCR) in corneal scrapings from patients with bacterial keratitis. Methods: A total of 65 patients with clinic...

2017
Delicia Shu Qin Ooi Verena Ming Hui Tan Siong Gim Ong Yiong Huak Chan Chew Kiat Heng Yung Seng Lee

INTRODUCTION The human salivary (AMY1) gene, encoding salivary α-amylase, has variable copy number variants (CNVs) in the human genome. We aimed to determine if real-time quantitative polymerase chain reaction (qPCR) and the more recently available Droplet Digital PCR (ddPCR) can provide a precise quantification of the AMY1 gene copy number in blood, buccal cells and saliva samples derived from...

Journal: :Applied and environmental microbiology 2009
Qianqian Liu Bassem Allam Jackie L Collier

We developed a real-time quantitative PCR (qPCR) assay targeting the rRNA internal transcribed spacer region of the hard clam pathogen QPX. The qPCR assay was more sensitive than was histology in detecting clams with light QPX infections. QPX was detected in 4 of 43 sediment samples but in none of 40 seawater samples.

2017
Brad E. Wasserman Daniel E. Carvajal-Hausdorf Kenneth Ho Wendy Wong Natalie Wu Victor C. Chu Edwin W. Lai Jodi M. Weidler Michael Bates Veronique Neumeister David L. Rimm

Historically, mRNA measurements have been tested on several commercially available platforms, but none have gained broad acceptance for assessment of HER2. An mRNA measurement, as a continuous value, has the potential for use in adjudication of the equivocal category. Here we use a real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR) assay in a closed, single-use car...

Journal: :The Journal of molecular diagnostics : JMD 2011
Ellen Vancutsem Oriane Soetens Maria Breugelmans Walter Foulon Anne Naessens

We evaluated a previously described quantitative real-time PCR (qPCR) for quantifying and differentiating Ureaplasma parvum and U. urealyticum. Because of nonspecific reactions with Staphylococcus aureus DNA in the U. parvum PCR, we developed a modified qPCR and designed new primers. These oligonucleotides eradicated cross-reactions, indicating higher specificity. The detection limits of the qP...

Journal: :Current issues in molecular biology 2014
Vija yJ Gadkar Martin Filion

Real time-quantitative PCR (RT-qPCR) technology has revolutionized the detection landscape in every area of molecular biology. The fundamental basis of this technology has remained unchanged since its inception, however various modifications have enhanced the overall performance of this highly versatile technology. These improvements have ranged from changes in the individual components of the ...

2009
Ramon Goni Patricia García Sylvain Foissac

Since the invention of real-time PCR (qPCR), thousands of high-impact studies have been conducted and published using qPCR technique (Heid et al. 1996; Higuchi et al. 1993; VanGuilder, Vrana, and Freeman 2008). Because it is highly sensitive, qPCR is the preferred method for microarray data validation (Canales et al. 2006); however the most exciting applications have been in the discovery of ne...

Journal: :Journal of clinical microbiology 2015
Gemma L Johnson Shah-Jalal Sarker Francesco Nannini Arianna Ferrini Emma Taylor Cornelia Lass-Flörl Wolfgang Mutschlechner Stephen A Bustin Samir G Agrawal

Clinical experience with the impact of serum biomarkers for invasive fungal disease (IFD) varies markedly in hemato-oncology. Invasive pulmonary aspergillosis (IPA) is the most common manifestation, so we evaluated biomarkers in bronchoalveolar lavage (BAL) fluid. An Aspergillus-specific lateral-flow device (LFD), quantitative real-time PCR (qPCR), and the galactomannan (GM) test were used with...

2008
Jack M. Gallup Mark R. Ackermann

The purpose of this manuscript is to describe a reliable approach to quantitative real-time polymerase chain reaction (qPCR) assay development and project management, which is currently embodied in the Excel 2003-based software program named "PREXCEL-Q" (P-Q) (formerly known as "FocusField2-6Gallup-qPCRSet-upTool-001," "FF2-6-001 qPCR set-up tool" or "Iowa State University Research Foundation [...

2018
Kun Lu Tian Li Jian He Wei Chang Rui Zhang Miao Liu Mengna Yu Yonghai Fan Jinqi Ma Wei Sun Cunmin Qu Liezhao Liu Nannan Li Ying Liang Rui Wang Wei Qian Zhanglin Tang Xinfu Xu Bo Lei Kai Zhang Jiana Li

Real-time quantitative polymerase chain reaction (qPCR) is one of the most important methods for analyzing the expression patterns of target genes. However, successful qPCR experiments rely heavily on the use of high-quality primers. Various qPCR primer databases have been developed to address this issue, but these databases target only a few important organisms. Here, we developed the qPrimerD...

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