نتایج جستجو برای: pcr and rt

تعداد نتایج: 16854480  

Journal: :iranian journal of virology 0
a ahmadi-vasmehjani department of microbiology, jahrom university of medical sciences, jahrom, iran sd mousavi-nasab department of virology, faculty of medical sciences, tarbiat modares university, tehran, iran r baharlou department of microbiology, jahrom university of medical sciences, jahrom, iran f jeirani department of fmd, razi vaccine and serum research institute, karaj, iran m shayestehpour department of virology, tehran university of medical sciences, tehran, iran s yaghoubi department of microbiology, tehran university of medical sciences, tehran, iran

background and aims: accurate and rapid diagnosis is necessary for effective control and prevention of foot-and-mouth disease (fmd). in present study, was evaluated real time reverse transcription-polymerase chain reaction (rrt-pcr) assay along with diagnostic routine methods for the detection of all seven serotypes of fmd virus (fmdv), namely o, c, a, sat1, 2, 3 and asia 1 in biological sample...

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: :Infectious diseases and clinical microbiology 2023

Objective: Reverse transcriptase loop-mediated isothermal amplification (RT-LAMP) is one of the time-saving, accurate, and cost-effective alternative methods to real-time polymerase chain reaction (RT-PCR). This study aimed identify robustness a colorimetric RT-LAMP assay kit that we developed, detecting SARS-COV-2 viral RNA within 30 minutes using primer set special N gene against RT-PCR, gold...

Journal: :BioTechniques 1996

Journal: :archives of razi institute 2016
a. shoshtari f. jeirani h. mahravani s.m. azimi

during 2009-10, real time rt-pcr and conventional rt-pcr techniques used for detecting btvs rna in 310 blood samples. for real time and gel based rt-pcr segment-1 and segment-10 selected as conserve genes to search any btv strains. using these methods, 58 (%18.7) and 14 (%4.5) positive samples were detected among the clinically suspected sheep. sensitivity of both molecular techniques evalua...

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