نتایج جستجو برای: sybr green i

تعداد نتایج: 1167642  

2016
Rachel V. Purcell John Pearson Frank A. Frizelle Jacqueline I. Keenan

Gut colonization with enterotoxigenic Bacteroides fragilis (ETBF) appears to be associated with the development of colorectal cancer. However, differences in carriage rates are seen with various testing methods and sampling sites. We compared standard PCR, SYBR green and TaqMan quantitative PCR (qPCR) and digital PCR (dPCR) in detecting the B. fragilis toxin (bft) gene from cultured ETBF, and f...

Journal: :Applied and environmental microbiology 2002
Narayanan Jothikumar Mansel W Griffiths

A SYBR Green LightCycler PCR assay using a single primer pair allowed simultaneous detection of stx1 and/or stx2 of Escherichia coli O157:H7. A distinct sequence of the Shiga-like toxin genes was amplified to yield products of 227 and/or 224 bp, respectively. The two products were distinguished by melting point curve analysis.

Journal: :genetics in the 3rd millennium 0
مینا حیات نوسعید mina hayat nosaeid molecular medicine department, biotechnology research center, pasteur institute of iran, tehran, iran رضا مهدیان reza mahdian سمیه جمالی somayeh jamali مرضیه رئیسی marzieh raeisi فهیمه مریمی fahimeh mariami صادق باباشاه sadegh babashah شبنم وحیدپور

mutations in the dystrophin gene cause duchenne muscular dystrophy (dmd), the most commonly inherited neuromuscular disorder, and becker muscular dystrophy (bmd), the milder allelic form of the disease. the mutation spectrum within this gene is unusual in that deletion of one or more exons are found in ~65% of cases. since no effective treatment is so far available for these diseases, the ident...

Journal: :Journal of clinical microbiology 2000
J Pietilä Q He J Oksi M K Viljanen

To differentiate the Borrelia burgdorferi sensu lato genospecies, LightCycler real-time PCR was used for the fluorescence (SYBR Green I) melting curve analysis of borrelial recA gene PCR products. The specific melting temperature analyzed is a function of the GC/AT ratio, length, and nucleotide sequence of the amplified product. A total of 32 DNA samples were tested. Of them three were isolated...

Journal: :Journal of medical microbiology 2003
Corinne F L Amar Paul H Dear Jim McLauchlin

A nested PCR assay (TPILC-PCR) was developed to detect and distinguish between Giardia duodenalis assemblages A and B from human faeces by analysis of the triose phosphate isomerase gene (tpi). The assay comprised an initial multiplexed block-based amplification. This was followed by two separate real-time PCR assays specific for assemblages A and B using a LightCycler and SYBR Green I to ident...

Journal: :Veterinaria italiana 2015
Mayurkumar Bhimani Bharat Bhanderi Ashish Roy

Twenty two isolates of Pasteurella multocida were obtained from different tissues of dead birds and animals (cattle, buffalo, sheep, and goat) suspected of fowl cholera and haemorrhagic septicaemia. The isolates were confirmed as P. multocida by various biochemical tests and PM PCR. An attempt was made to standardize Loop mediated isothermal amplification (LAMP) using newly designed primer sequ...

Journal: :Food and Nutrition Sciences 2021

Salmonella enterica serovars is a leading cause of human gastroenteritis, and the incidence of salmonellosis constantly increasing, causing millions infections and many deaths annually. The detection pathogen in optimal terms an essential factor for reducing impact on body. In this work, SYBR Green I-based qPCR method quantification was developed validated. For subsp. enterica, two pairs pr...

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