نتایج جستجو برای: rflp pcr typing

تعداد نتایج: 196114  

Journal: :Applied and environmental microbiology 1998
M Li T Masuzawa N Takada F Ishiguro H Fujita A Iwaki H Wang J Wang M Kawabata Y Yanagihara

Fifty-nine Borrelia burgdorferi sensu lato culture isolates collected from northeastern China were characterized by 5S-23S rRNA intergenic spacer restriction fragment length polymorphism (RFLP) analysis and reactivity with monoclonal antibodies (MAbs). Among 59 culture isolates, 30 (50.8%) were Borrelia garinii and 17 (28.8%) were Borrelia afzelii, 2 were mixtures composed of B. garinii with RF...

Journal: :Investigative ophthalmology & visual science 2001
A K Adhikary J Numaga T Kaburaki H Kawashima S Kato M Araie K Miyata H Shimizu F Yagyu E Suzuki H Ushijima

PURPOSE To develop a new detection and typing method of oculopathogenic strains of subgenus D adenoviruses directly from conjunctival scrapings by a combination of polymerase chain reaction (PCR) and restriction enzyme analysis (REA). METHODS A new PCR method using primer pairs of AF2/AR2, which are specific for the fiber genes, were developed to amplify 1150-bp products from nine oculopathog...

Journal: :Polish journal of veterinary sciences 2011
J Karakulska A Pobucewicz P Nawrotek M Muszyńska A J Furowicz D Czernomysy-Furowicz

The aim of this study was molecular identification of S. aureus strains isolated from mastitic milk samples and establishing the genetic relationship between strains isolated from cows belonging to the same herd. In all 43 isolated strains the gap gene (930 bp) was amplified, which enabled their affiliation to the Staphylococcus genus to be established. PCR-RFLP with AluI endonuclease of the ga...

2014
Fatemeh Shakeri Ezzat Allah Ghaemi Maya Babai Kochkaksaraei

BACKGROUND Protein A is the virulence factors of Staphylococcus aureus rolling in its pathogenesis, and its gene is used for typing. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) with different enzymes has been used for this action. OBJECTIVES In this study, we used Bsp143I enzyme for digestion of the gene, coding protein A (spa gene) in S. aureus. The bacteria...

Journal: :jundishapur journal of microbiology 0
reza mirnejad molecular biology research center, baqiyatallah university of medical sciences, tehran, ir iran mozafar mohammadi molecular biology research center, baqiyatallah university of medical sciences, tehran, ir iran ali majdi young researchers club, tonekabon branch, islamic azad university, tonekabon, ir iran niloufar taghizoghi bounty house, stowage, bellerbys college, london, united kingdom vahhab piranfar department of biology, tonekabon branch, islamic azad university of tonekabon, tonekabon, ir iran; department of biology, tonekabon branch, islamic azad university of tonekabon, tonekabon, ir iran. tel: +98-937 130 7300, fax: +98-2188039883

conclusions the results of this study showed that pcr–rflp technique was a fast and applicable method especially for separation, detection and differentiation between species of b. melitensis and b. abortus biovars in blood sample. also the presented data showed that b. melitensis biovar 1 was the prevalence biovar. background brucella is an intracellular parasite of the disease brucellosis thr...

Journal: :Journal of clinical microbiology 2010
Nicolas Radomski Virginie C Thibault Claudine Karoui Krystel de Cruz Thierry Cochard Cristina Gutiérrez Philip Supply Frank Biet María Laura Boschiroli

Members of the Mycobacterium avium complex (MAC) are ubiquitous bacteria that can be found in water, food, and other environmental samples and are considered opportunistic pathogens for numerous animal species, mainly birds and pigs, as well as for humans. We have recently demonstrated the usefulness of a PCR-based mycobacterial interspersed repetitive-unit-variable-number tandem-repeat (MIRU-V...

Journal: :Turkish journal of medical sciences 2016
Tekin Karslıgil Ayşen Bayram Fahriye Ekşi

BACKGROUND/AIM The purpose of the present study was to determine the distribution and epidemiological features of mycobacteria with molecular methods. MATERIALS AND METHODS Fifty-five culture-positive samples were analyzed by polymerase chain reaction-restriction enzyme length polymorphism (PCR-RFLP) at species level, and their molecular typing was performed with spoligotyping. The IS6110 reg...

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