نتایج جستجو برای: touchdown nested pcr

تعداد نتایج: 200307  

1980
Farhad Safarpoor Dehkordi

Problem statement: Q fever is a ubiquitous zoonosis caused by Coxiella burnetii, an obligate intracellular rickettsial organism that caused abortion and stillbirth in ruminants. Approach: The prevalence of Coxiella burnetii in Iran is essentially unknown. Its traditional diagnosis is based on culture, serology and conventional PCR. In this present study, for more sensitive and accurate detectio...

2017
Shotaro Izumi Kyuma Suzuki

For the rapid identification and detection of Vibrio anguillarum, we have PCR amplification technique targeting gyrB region has been evaluated. We have designed twosets of PCR primers for the specific amplification of gyrB in V. anguillarum using single and nested PCR. PCRs specificity was demonstrated by successful amplicon from V. anguillarum DNA. The detection limit of the single PCRs and th...

Journal: :Applied and environmental microbiology 1999
M Cook W H Lynch

A nested reverse transcriptase (RT) PCR assay detected mRNA of the salmonid pathogen Renibacterium salmoninarum in samples of RNA extracts of between 1 and 10 cells. Total RNA was extracted from cultured bacteria, Atlantic salmon (Salmo salar L.) kidney tissue and ovarian fluid seeded with the pathogen, and kidney tissue from both experimentally challenged and commercially raised fish. Followin...

2016
Madhavi L. Kakumanu Loganathan Ponnusamy Haley T. Sutton Steven R. Meshnick William L. Nicholson Charles S. Apperson

A novel nested PCR assay was developed to detectRickettsiaspp. in ticks and tissue samples from humans and laboratory animals. Primers were designed for the nested run to amplify a variable region of the 23S-5S intergenic spacer (IGS) ofRickettsiaspp. The newly designed primers were evaluated using genomic DNA from 11Rickettsiaspecies belonging to the spotted fever, typhus, and ancestral groups...

آریا بدیعی امیر حمیدی عباس برین فرهاد موسی خانی, محسن ظفری

عامل بیماری یون، باکتری مایکوباکتریوم آویوم تحت گونه پاراتوبرکولوزیس است و هر ساله زیان فراوانی در سطح جهانی، از قبیل کاهش تولید، افت شاخص­های تولید مثلی و حذف دام مبتلا را متوجه صنعت گاو شیری، می‏نماید. از دیگر سوی، این باکتری را یک پاتوژن زئونوز می­دانند و تحقیقات جدید احتمال می­دهند که این باکتری در ایجاد بیماری کرون در انسان، نقش داشته باشد. هدف این مطالعه مقایسه روش‏های تشخیص آزمایشگاهی ال...

2015
Hossein Meghdadi Azar D. Khosravi Ata A. Ghadiri Amir H. Sina Ameneh Alami

Present study was aimed to examine the diagnostic utility of polymerase chain reaction (PCR) and nested PCR techniques for the detection of Mycobacterium tuberculosis (MTB) DNA in samples from patients with extra pulmonary tuberculosis (EPTB). In total 80 formalin-fixed, paraffin-embedded (FFPE) samples comprising 70 samples with definite diagnosis of EPTB and 10 samples from known non- EPTB on...

Journal: :Turkish journal of medical sciences 2016
Cheronie Shely Stanis Beng Kah Song Tock Hing Chua Yee Ling Lau Jenarun Jelip

BACKGROUND/AIM Malaria is a major public health problem, especially in the Southeast Asia region, caused by 5 species of Plasmodium (P. falciparum, P. vivax, P. malariae, P. ovale, and P. knowlesi). The aim of this study was to compare parasite species identification methods using the new multiplex polymerase chain reaction (PCR) against nested PCR and microscopy. MATERIALS AND METHODS Blood ...

Parviz Shayan Vahid Noaman,

Anaplasma bovis is a leukocytotropic agent of bovine anaplasmosis and there is no available information about molecular study on this agent in cattle of Iran. In this study a total 150 cattle blood samples were collected from central part of Iran. The presence of A. bovis examined using light microscopic detection and species-specific nested polymerase chain reaction (nested-PCR) based on 16S r...

Journal: :Journal of clinical microbiology 1997
X Forns D Tan H J Alter R H Purcell J Bukh

Serum samples from 96 Spanish hemodialysis patients, as well as serial dilutions of RNA extracted from a reference strain of hepatitis G virus (HGV), were tested for HGV or GB virus C (GBV-C) RNA. Two different reverse transcription (RT)-PCR-based methods of detection were compared for the ability to detect RNA extracted from the samples: an RT-nested PCR assay with primers derived from the 5' ...

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