نتایج جستجو برای: uniplex pcr

تعداد نتایج: 175088  

2017
Abdul Haque Asma Haque Muhammad Saeed Aysha Azhar Samreen Rasool Sidra Shan Beenish Ehsan Zohaib Nisar

Objectives Emergence of methicillin resistant Staphylococcus aureus (MRSA) is a major medical problem of current era. These bacteria are resistant to most drugs and rapid diagnosis can provide a clear guideline to clinicians. They possess specific virulence factors and relevant information can be very useful. We designed this study to develop multiplex PCRs to provide rapid information. Metho...

Journal: :Iranian journal of pathology 2016
Gholam Reza Irajian Faramarz Masjedian Jazi Reza Mirnejad Vahhab Piranfar Taghi Zahraei Salehi Noor Amir Mozafari Ehsanollah Ghaznavi-Rad Mahmoud Khormali

BACKGROUND Brucellosis is an endemic zoonotic disease in the Middle East. This study intended to design a uniplex PCR assay for the detection and differentiation of Brucella at the species level and determining the antibiotic susceptibility pattern of Brucella in Iran. METHODS Sixty-eight Brucella specimens (38 animal and 30 human specimens) were analyzed using PCR (using one pair of primers)...

Journal: :iranian journal of public health 0
reza ranjbar seyyed mojtaba mortazavi ali mehrabi tavana meysam sarshar ali najafi rahim soruri zanjani

background: salmonella enterica serovar typhi, as causative agent of typhoid fever, is one of the most important endemic pathogens. non-typhoidal salmonella serovars, including typhimurium , infantis , and enteritidis are amongst the most prevalent serotypes worldwide and in developing areas such as iran. the aim of this study was to apply a uniplex pcr for rapid detection of salmonella spp., a...

Journal: :iranian red crescent medical journal 0
nargess safari foroshani science and research islamic azad university, tehran, ir iran ali karami research center of molecular biology, baqiyatallah university of medical sciences, tehran, ir iran; ali karami, research center of molecular biology, baqiyatallah university of medical sciences, p.o. box: 19945-581, tehran, ir iran. tel: +98-2188039883, fax: +98-2188057023. fatemeh pourali research center of molecular biology, baqiyatallah university of medical sciences, tehran, ir iran

conclusion the designed methods are accurate, rapid, and inexpensive to find and differentiate these bacteria from similar bacteria. they can be applied for rapid diagnosis of these agents in different specimens, and bioterrorism cases. background salmonella typhi, bacillus anthracis, and yersinia pestis are some serious human pathogens, which their early diagnosis is of great importance. salmo...

Background: Brucellosis is an endemic zoonotic disease in the Middle East. This study intended to design a uniplex PCR assay for the detection and differentiation of Brucella at the species level and determining the antibiotic susceptibility pattern of Brucella in Iran. Methods: Sixty-eight Brucella specimens (38 an...

2015
Amy Bernardo Shan Wang Paul St. Amand Guihua Bai David D Fang

With the advent of next generation sequencing (NGS) technologies, single nucleotide polymorphisms (SNPs) have become the major type of marker for genotyping in many crops. However, the availability of SNP markers for important traits of bread wheat (Triticum aestivum L.) that can be effectively used in marker-assisted selection (MAS) is still limited and SNP assays for MAS are usually uniplex. ...

2015
Nelly Datukishvili Tamara Kutateladze Inga Gabriadze Kakha Bitskinashvili Boris Vishnepolsky

We present novel multiplex PCR methods for rapid and reliable screening of genetically modified organisms (GMOs). New designed PCR primers targeting four frequently used GMO specific sequences permitted identification of new DNA markers, in particular 141 bp fragment of cauliflower mosaic virus (CaMV) 35S promoter, 224 bp fragment of Agrobacterium tumefaciens nopaline synthase (NOS) terminator,...

2017
Jae Wook Hyun Rok Yeon Hwang Kyung Eun Jung

Satsuma dwarf virus (SDV) or Citrus mosaic sadwavirus (CiMV) were not consistently detected in RT-PCR assay with the primer sets based on gene of Japan isolates. SDV and CiMV isolates were distinctively divided into two groups based on phylogenetic analysis of PP2 gene cloned from 22 Korean isolates, and the Korean CiMV and SDV isolates shared 95.5-96.2% and 97.1-97.7% sequence identity with Ja...

Journal: :Indian journal of medical microbiology 2005
G Shyamal P Sowmya B Sudha J Malathi L K Therese H N Madhavan

PURPOSE To standardize and apply a polymerase chain reaction (PCR) on the glycoprotein D gene to differentiate Herpes simplex virus (HSV) 1 & 2 serotypes in culture negative intraocular specimens. METHODS Twenty-one intraocular fluids collected from 19 patients were subjected to cultures for HSV and uniplex PCR (uPCR) for DNA polymerase gene. To differentiate HSV serotypes, as 1 & 2, a semine...

2011
Qiuying Huang Linlin Zheng Yumei Zhu Jiafeng Zhang Huixin Wen Jianwei Huang Jianjun Niu Xilin Zhao Qingge Li

The target volume of multiplex real-time PCR assays is limited by the number of fluorescent dyes available and the number of fluorescence acquisition channels present in the PCR instrument. We hereby explored a probe labeling strategy that significantly increased the target volume of real-time PCR detection in one reaction. The labeling paradigm, termed "Multicolor Combinatorial Probe Coding" (...

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