نتایج جستجو برای: time nasba

تعداد نتایج: 1891542  

Journal: :The Analyst 2015
Quanli Liu Xuexia Lin Luyao Lin Linglu Yi Haifang Li Jin-Ming Lin

Research towards nucleic acid amplification technologies for detection of human papillomavirus (HPV) 16 E6/E7 mRNA was carried out in combination with microchip electrophoresis (MCE). The approaches of nucleic acid sequence based amplification (NASBA), one-step RT-PCR and two-step RT-PCR were successfully developed. NASBA was a simple enzymatic reaction, which directly amplified HPV16 mRNA by i...

, فروزنده مقدم, مهدی, جوادی, غلامرضا, صادقی زاده, مجید, ناظمی, علی, هاشمی, مهرداد,

سابقه و هدف: بیماران مبتلا به لوسمی میلوئیدی مزمن (CML) دارای کرموزوم فیلادلفیا هستند. این کروموزوم حاصل جابجایی بازوهای بلند کروموزوم های 9 و 22 (q34q11) بوده که منجر به ایجاد الحاق بین ژنهای BCR و ABL می گردد. در این مطالعه، تکنیک های RT-PCR و NASBA در تعیین رونویس های bcr-abl مقایسه شد.روش بررسی: رونویس های الحاقی بطور مصنوعی سنتز و RNA از رده سلولی لوسمیک K562 استخراج گردید. سریال رقت هم از...

Journal: :Journal of clinical microbiology 2000
R N Shepard J Schock K Robertson D C Shugars J Dyer P Vernazza C Hall M S Cohen S A Fiscus

Little information is available describing viral loads in body fluids other than blood. In addition, the suitability of commercially available assays for human immunodeficiency virus type 1 (HIV-1) RNA quantitation has not been evaluated in most nonblood fluids. We compared Organon Teknika's nucleic acid sequence-based amplification method (NASBA) and Roche's Amplicor HIV-1 Monitor (reverse tra...

Journal: :Journal of virological methods 1991
T Kievits B van Gemen D van Strijp R Schukkink M Dircks H Adriaanse L Malek R Sooknanan P Lens

Isothermal nucleic acid amplification of target RNA or DNA sequences is accomplished by the simultaneous enzymatic activity of AMV reverse transcriptase, T7 RNA polymerase and RNase H. Amplification factors of the nucleic acid sequence based amplification (NASBA) method range from 2 x 10(6) to 5 x 10(7) after 2.5 h incubation at 41 degrees C. During NASBA there is a major accumulation of specif...

Journal: :Applied and environmental microbiology 2004
Julie Jean Doris H D'Souza Lee-Ann Jaykus

Human enteric viruses are currently recognized as one of the most important causes of food-borne disease. Implication of enteric viruses in food-borne outbreaks can be difficult to confirm due to the inadequacy of the detection methods available. In this study, a nucleic acid sequence-based amplification (NASBA) method was developed in a multiplex format for the specific, simultaneous, and rapi...

2010
Enock Matovu Claire M. Mugasa Rosine Ali Ekangu Stijn Deborggraeve George W. Lubega Thierry Laurent Gerard J. Schoone Henk D. Schallig Philippe Büscher

BACKGROUND The polymerase chain reaction (PCR) and nucleic acid sequence-based amplification (NASBA) have been recently modified by coupling to oligochromatography (OC) for easy and fast visualisation of products. In this study we evaluate the sensitivity and specificity of the PCR-OC and NASBA-OC for diagnosis of Trypanosoma brucei gambiense and Trypanosoma brucei rhodesiense human African try...

Journal: :Lab on a chip 2008
Ivan K Dimov Jose L Garcia-Cordero Justin O'Grady Claus R Poulsen Caroline Viguier Lorcan Kent Paul Daly Bryan Lincoln Majella Maher Richard O'Kennedy Terry J Smith Antonio J Ricco Luke P Lee

We demonstrate the first integrated microfluidic tmRNA purification and nucleic acid sequence-based amplification (NASBA) device incorporating real-time detection. The real-time amplification and detection step produces pathogen-specific response in < 3 min from the chip-purified RNA from 100 lysed bacteria. On-chip RNA purification uses a new silica bead immobilization method. On-chip amplific...

Journal: :Japanese journal of infectious diseases 2015
Yoshiko Sugita-Konishi Yutaka Fukuda Koh-ichiro Mori Toru Mekata Toyohiko Namba Makoto Kuroda Akiko Yamazaki Takahiro Ohnishi

Kudoa septempunctata is a newly identified causative agent of foodborne diseases associated with consuming raw olive flounder. Qualitative PCR and quantitative real-time PCR have been used as notification methods to identify K. septempunctata in Japan. However, these methods require expensive equipment and are time-consuming (2-3 h for screening). To address these problems, in this study, we de...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس - دانشکده علوم پزشکی 1386

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