نتایج جستجو برای: standard pcr

تعداد نتایج: 683958  

Journal: :Clinical chemistry 2014
Ward De Spiegelaere Eva Malatinkova Lindsay Lynch Filip Van Nieuwerburgh Peter Messiaen Una O'Doherty Linos Vandekerckhove

BACKGROUND Quantification of integrated proviral HIV DNA by repetitive-sampling Alu-HIV PCR is a candidate virological tool to monitor the HIV reservoir in patients. However, the experimental procedures and data analysis of the assay are complex and hinder its widespread use. Here, we provide an improved and simplified data analysis method by adopting binomial and Poisson statistics. METHODS ...

Journal: :Journal of clinical microbiology 2001
P Y Shi E B Kauffman P Ren A Felton J H Tai A P Dupuis S A Jones K A Ngo D C Nicholas J Maffei G D Ebel K A Bernard L D Kramer

The recent outbreaks of West Nile virus (WNV) in the northeastern United States and other regions of the world have made it essential to develop an efficient protocol for surveillance of WNV. In the present report, we describe a high-throughput procedure that combines automated RNA extraction, amplification, and detection of WNV RNA. The procedure analyzed 96 samples in approximately 4.5 h. A r...

Journal: :تحقیقات دامپزشکی 0
احمد مرشدی ملاحت احمدی تقی زهرایی صالحی پریسا سقایی

brusellosis is one of the most dangerous infectious zoonotic diseases which at present affect most areas of iran directly or indirectly.the aim of the present study was evaluate the efficacy of pcr test in detection of brucellosis. suspected animal sera (n=20) to brusellosis were collected from clinics and subjected to rose bengal and wright agglutination tests and to pcr analysis. while 6 samp...

Journal: :iranian journal of parasitology 0
amir bairami sasan rezaei mostafa rezaeian

background: among the most important parasitic disease, causing diarrhea, gi­ardia lamblia is noteworthy. nowadays detection methods for these parasites in­clude parasitological methods such as microscopic examination. the sensitivity of these methods relies on the expertise and experience of examiners. in contrast, molecular methods such as pcr are less dependent on the expertise of the exam­i...

Journal: :Journal of clinical microbiology 1996
M Maher M Glennon G Martinazzo E Turchetti S Marcolini T Smith M T Dawson

We report on a PCR-based assay we have developed for the detection of Mycobacterium tuberculosis in sputum samples. One hundred sputum specimens, which included 34 culture-positive and 66 culture-negative specimens, were evaluated with this system. Of the 34 culture-positive specimens, 31 were PCR positive, and 60 of the culture-negative specimens were PCR negative. An internal standard has bee...

Journal: :Microbiology Australia 2022

Dermatophyte fungi are a common cause of skin, nail and hair infections globally, ranging from mild to cosmetically disfiguring, or even invasive in rare cases. Specimens requiring fungal microscopy culture for suspected dermatophyte infection make up significant portion the workload diagnostic microbiology laboratories. Whilst still considered gold standard, culture-based method is labour inte...

2012
Jingzi Piao Jun Jiang Bianli Xu Xiaohong Wang Yanfang Guan Weili Wu Licheng Liu Yuan Zhang Xueyong Huang Pengzhi Wang Jinyin Zhao Xiaoping Kang Hua Jiang Yuanyin Cao Yuling Zheng Yongqiang Jiang Yan Li Yinhui Yang Weijun Chen

Simultaneous detection of enteric viruses that cause similar symptoms (e.g. hand, foot and mouth disease) is essential to the prevention of outbreaks and control of infections. In this study, a novel PCR-Mass assay combining multiplex polymerase chain reaction (PCR) with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) was developed and used for simult...

Journal: :BioTechniques 1997
A Möller J K Jansson

Competitive PCR (cPCR) is a quantitative PCR approach based on the addition of an internal standard to the PCR mixture. In this study, cPCR was used to quantitate genetically tagged cyanobacteria in Baltic Sea sediment. The cyanobacterium Synechocystis 6803-luc has a chromosomal insertion of the firefly luciferase gene, luc, as a marker detectable by PCR. A competitive standard was constructed ...

Journal: :BioTechniques 1998
P C Guenthner C E Hart

We have developed a quantitative competitive PCR (QC-PCR) assay in a microplate format for quantifying human immunodeficiency virus Type 1 (HIV-1) DNA or RNA in a broad range of source materials. Our QC-PCR assay is a modification of technique originally described by Piatak et al. (1993), which is based on the presence of a competitive internal standard containing an internal 80-bp deletion of ...

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