نتایج جستجو برای: rt pcr nested pcr

تعداد نتایج: 222624  

Journal: :The Journal of veterinary medical science 1999
T Mizutani Y Nishino H Kariwa I Takashima

Several methods for the detection of Borna disease virus (BDV) RNA have been reported, one being the reverse transcription-nested polymerase chain reaction (RT-nested PCR) method. However, due to the possibility of contamination of the cloned DNA in a reaction tube, false-positive results might be obtained by RT-nested PCR. To detect only BDV RNA without anxiety of contamination, we developed a...

Journal: :iranian journal of biotechnology 2007
massoud talebkhan garoussi mohammad reza bassami seyed ehsan afshari

bovine viral diarrhoea virus (bvdv) is an important pathogen of dairy cattle. in this study, bulk milk samples representing a total of 4105 milking cows, from 18 dairy cattle herds in the suburb of mashhad- iran, were tested for presence of bvdv by the use of a nested reverse transcription polymerase chain reaction (nested rt- pcr) assay. non of the cows in the herds had been vaccinated against...

Journal: :Methods in molecular biology 2015
Xuelian Yu Reena Ghildyal

Human rhinoviruses (HRVs) are positive-stranded RNA viruses belonging to the Enterovirus genus in the family of Picornaviridae. Identification of the specific strain in HRV disease has been difficult because the traditional serological method is insensitive, labor intensive, and cumbersome. With the fast progress in molecular biological technique, more sensitive and faster molecular methods hav...

ژورنال: علمی شیلات ایران 2019

بیماری نکروز عصبی ویروسی، یکی از مهمترین بیماری‌‌های ویروسی با گسترش جهانی در ماهیان دریایی و پرورشی دنیا محسوب می‌‌شود و تا به امروز بیش از 70 گونه حساس ماهی به این بیماری شناسایی شده است. هدف از این پژوهش ردیابی و شناسایی سریع ویروس مذکور با استفاده از روش Nested RT-PCR از بافت مغز کفال ماهیان دریای خزر بود. در طول فصل صید در سال 1395 تعداد 40 قطعه کفال طلایی (Liza aurata) در محدوده وزنی 50  ...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تبریز - دانشکده دامپزشکی 1391

تعداد 140 نمونه خون کامل (از شهرهای بندرعباس، کامیاران، پیرانشهر، پلدشت و ماکو، لاهیجان، قروه و بیله سوار از هرکدام 20 نمونه ی خون گوسفند و بز به تعداد مساوی از هر دو جنس) به وسیله ونوجکت به میزان 5-10 میلی لیتر همراه با edta از گوسفند و بز برخی مناطق مرزی ایران بطور تصادفی اخذ شده و در مجاورت یخ به آزمایشگاه ارسال می گردد. هدف از انتخاب نقاط ذکر شده، وجود نشانه های غیر اختصاصی از بیماری زبان آ...

Journal: :Veterinary microbiology 2005
Renata S Almeida Fernando R Spilki Paulo M Roehe Clarice W Arns

A reverse transcriptase (RT)-nested-polymerase chain reaction (PCR) was standardised to detect bovine respiratory syncytial virus (BRSV), using a Brazilian isolate, in three experimentally infected calves. This followed initial tests in infected chicken embryo related (CER) cells. One animal had lesions, characterized by interstitial multifocal pneumonia, severe interstitial and subpleural emph...

Journal: :Applied and environmental microbiology 1998
J Green K Henshilwood C I Gallimore D W Brown D N Lees

We describe the evaluation of a nested reverse transcriptase PCR (RT-PCR) procedure for the detection of small round-structured viruses (SRSVs) in molluscan shellfish and the application of this assay for the detection of SRSVs in commercially produced shellfish and in shellfish implicated in outbreaks of gastroenteritis. The range of virus strains detected and the sensitivity of detection were...

Journal: :Revista do Instituto de Medicina Tropical de Sao Paulo 2000
N S Gonçales F F Costa J Vassallo F L Gonçales

Screening blood donations for anti-HCV antibodies and alanine aminotransferase (ALT) serum levels generally prevents the transmission of hepatitis C virus (HCV) by transfusion. The aim of the present study was to evaluate the efficiency of the enzyme immunoassay (EIA) screening policy in identifying potentially infectious blood donors capable to transmit hepatitis C through blood transfusion. W...

Journal: :Journal of clinical microbiology 2001
C Steininger S W Aberle T Popow-Kraupp

The development of a rhinovirus (RV)-RNA-specific reverse transcription (RT)-PCR assay is complicated by the close homology between the RV and enterovirus (EV) genomes in the highly conserved 5'-noncoding region, which is chosen for primer design in most RT-PCR assays. We have developed a sensitive, rapid, and RV-specific nested RT-PCR assay and have used it to test nasopharyngeal aspirates fro...

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