نتایج جستجو برای: rflp and pcr

تعداد نتایج: 16852787  

Journal: :Applied and environmental microbiology 2004
S Rousseaux M Olier J P Lemaître P Piveteau J Guzzo

A PCR-restriction fragment length polymorphism (RFLP) method was developed in order to screen a large number of strains for impaired adhesion to epithelial cells due to expression of truncated InlA. inlA polymorphism was analyzed by PCR-RFLP in order to correlate inlA PCR-RFLP profiles and production of truncated InlA. Thirty-seven Listeria monocytogenes strains isolated from various sources, i...

ژورنال: :زیست شناسی میکروارگانیسم ها 0
محمد ارجمند زادگان استادیار باکتری شناسی پزشکی، دانشگاه علوم پزشکی اراک، ایران توکتم پولاد دانشجوی کارشناسی ارشد میکروبیولو‍ژی، دانشگاه آزاد اسلامی، واحد علوم تحقیقات کردستان، ایران مانا شجاع پور دانشجوی دکتری تخصصی پزشکی مولکولی، مرکز تحقیقات پزشکی و مولکولی، دانشگاه علوم پزشکی اراک، ایران اعظم احمدی دانشجوی دکتری تخصصی ژنتیک مولکولی، مرکز تحقیقات سل و عفونی کودکان، دانشگاه علوم پزشکی اراک، ایران بهاره رحیمیان ظریف فاطمه صالحی دانشجوی کارشناسی ارشد میکروبیولوژی، دانشگاه آزاد اسلامی، واحد علوم تحقیقات کردستان، ایران

مقدمه: در این تحقیق، برای تشخیص سریع مقاومت به کانامایسین، آمیکاسین، کاپرئومایسین، چند روش مولکولی طراحی و مقایسه شدند.   مواد و روش ‏‏ ها: از میان 120 سویه کلینیکی مایکوباکتریوم توبرکلوزیس، 70 سویه برای بررسی موتاسیون ‏ها ی احتمالی انتخاب شدند. در روش pcr-rflp ‏ از آنزیم ajii برای تشخیص سویه وحشی و از آنزیم bstfni برای شناسایی سویه موتانت استفاده شد. علاوه بر این، در طراحی روش آلل اسپسیفیک همز...

2010
V Noaman P Shayan

BACKGROUND AND OBJECTIVES In Iran, anaplasmosis is normally diagnosed with traditional Giemsa staining method. This is not applicable for identification of the carrier animals. The aim of this study was to compare the detection of Anaplasma marginale in two different numbers of microscopic fields (50 and 100) using conventional Giemsa staining method compared with the PCR-RFLP technique. MATE...

2009
N Maleki-Ravasan MA Oshaghi E Javadian Y Rassi J Sadraei F Mohtarami

BACKGROUND We aimed to develop a PCR-RFLP assay based on available sequences of putative vertebrate hosts to identify blood meals ingested by field female sand fly in the northwest of Iran. In addition, the utility of PCR-RFLP was compared with ELISA as a standard method. METHODS This experimental study was performed in the Insect Molecular Biology Laboratory of School of Public Health, Tehra...

Journal: :The Indian journal of medical research 2007
P Sowmya V Dhanya H N Madhavan K L Therese

BACKGROUND & OBJECTIVE Glycoprotein B (gB), involved in cell-to-cell transmission of human cytomegalovirus (HCMV), is a critical factor in tissue tropism and viral pathogenesis. The aim of the present study was to compare the efficiency of PCR-based RFLP and multiplex nested PCR for gB gene of HCMV to determine their genotype in clinical specimens from patients with HCMV. METHODS The PCR base...

Journal: :Genitourinary medicine 1995
Q C Lau V T Chow C L Poh

OBJECTIVES To employ polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) analysis for the rapid differentiation of Neisseria gonorrhoeae protein IB (PIB) isolates and to compare its usefulness with the widely accepted auxotype/serovar classification scheme. METHODS The outer membrane protein IB genes of 47 gonococcal isolates belonging to 10 different serovars ...

Journal: :Acta veterinaria Hungarica 2013
Boglárka Sellyei Eva Ivanics Tibor Magyar

The 16 somatic serotype type strains and 60 field isolates of Pasteurella multocida, representing various avian species and geographic regions in Hungary, were characterised by PCR-restriction fragment length polymorphism (PCR-RFLP) analysis of the ompH gene with DraI restriction endonuclease. The type strains yielded eight different (I-VIII) profiles. Strains whose PCR fragment was uncut by Dr...

2011
Jana FRÁNOVÁ

Polymerase chain reaction (PCR) with subsequent restriction fragment length polymorphism (RFLP) analysis is often used for phytoplasma identification and classification. Although these techniques are very sensitive and specific, in some cases, nonspecific reactions, false positives and negatives results, as well as unusual or illegible profiles after RFLP analyses, amplification of plant host ́s...

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