نتایج جستجو برای: Keywords:Chicken SYBR Green RT-PCR16S rRNA Burger Sausage

تعداد نتایج: 231370  

Journal: :iran agricultural research 2016
l. lakzadeh s. hosseinzadeh s.s. shekarforoush m. fazeli

abstract- today, the authenticity of meat products with less costly and desirable species has increased. therefore and considering religious, economicalor public health concerns, proper actions should be taken to prevent such frauds. in this study, real time pcr assay was applied for rapid, sensitive and specific identification and quantification of chicken tissue in meat products. specific pri...

L. Lakzadeh M. Fazeli S. Hosseinzadeh S.S. Shekarforoush

ABSTRACT- Today, the authenticity of meat products with less costly and desirable species has increased. Therefore and considering religious, economicalor public health concerns, proper actions should be taken to prevent such frauds. In this study, real time PCR assay was applied for rapid, sensitive and specific identification and quantification of chicken tissue in meat products. Specific pri...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شیراز - دانشکده دامپزشکی 1391

در این مطالعه از pcr معمولی و real time pcr با استفاده از ژن میتوکندریایی s rrna 12 مرغ برای جداسازی و تعیین مقدار خمیر مرغ در نمونه های غذایی استفاده گردید. نمونه ها شامل غلظت های مختلف dna مرغ، نمونه های تجاری سوسیس و همبرگر و نمونه های تجربی شامل غلظت های مختلف خمیر مرغ که تحت دماهای مختلف حرارت داده شدند، بودند. نتایج نشان داد که pcr با پرایمر اختصاصی گونه می تواند تا غلظت 01/0 نانوگرم dna ...

2014
R. Tedjo Sasmono Aryati Aryati Puspa Wardhani Benediktus Yohan Hidayat Trimarsanto Sukmal Fahri Tri Y. Setianingsih Febrina Meutiawati

Diagnostic tests based on detection of dengue virus (DENV) genome are available with varying sensitivities and specificities. The Simplexa Dengue assay (Focus Diagnostics) is a newly developed real-time RT-PCR method designed to detect and serotype DENV simultaneously. To assess the performance of the Simplexa Dengue assay, we performed comparison with conventional RT-PCR and SYBR Green real-ti...

Journal: :Journal of clinical microbiology 2003
Pei-Yun Shu Shu-Fen Chang Yu-Chung Kuo Yi-Yun Yueh Li-Jung Chien Chien-Lin Sue Ting-Hsiang Lin Jyh-Hsiung Huang

A quantitative one-step SYBR Green I-based reverse transcription (RT)-PCR system was developed for the detection and differentiation of four different dengue virus serotypes in acute-phase serum samples. A set of group- and serotype-specific primer pairs was designed against conserved sequences in the core region and evaluated for clinical diagnosis. A linear relationship was obtained between t...

2006
Khalid Munir

We have previously described the development of a onetube SYBR Green real-time RT-PCR assay for the detection and quantitation of infectious salmon anemia virus (ISAV) in various biological samples. The twofold aim of the present study was to verify that the optimized SYBR Green real-time RT-PCR conditions could detect ISAV isolates of different geographic origins, and to analyze the growth pat...

Journal: :Journal of virological methods 2006
Aniko Varga Delano James

Real-time RT-PCR and SYBR green I melt curve analysis of a 74 bp amplicon enabled identification of Plum pox virus strains C, EA, and W, with distinct T(m)'s associated with each strain. This test is a useful supplement to a real-time RT-PCR test described earlier that was used to distinguish PPV strains D and M. A longer fragment of 155 bp was not effective for strain identification. A simplif...

Journal: :Molecular vision 2000
D A Simpson S Feeney C Boyle A W Stitt

PURPOSE To determine whether continuous monitoring of SYBR Green I fluorescence provides a reliable and flexible method of quantitative RT-PCR. Our aims were (i) to test whether SYBR Green I analysis could quantify a wide range of known VEGF template concentrations, (ii) to apply this method in an experimental model, and (iii) to determine whether 20 existing primer pairs could be used to quant...

Journal: :jundishapur journal of microbiology 0
mohammad soleimani department of microbiology, qom branch, islamic azad university, qom, ir iran; department of microbiology, qom branch, islamic azad university, qom, ir iran, p.o. box: 37185/364. tel:+98-2517780001, fax: +98-2517780001 mohammad reza zolfaghari department of microbiology, qom branch, islamic azad university, qom, ir iran abbas morovvati department of microbiology, qom branch, islamic azad university, qom, ir iran

background aggregatibacter actinomycetemcomitans and tannerella forsythensis are two major pathogens in destructive periodontal disease in humans. the detection of these bacteria is needed for diagnosis and management of the mentioned diseases. objectives we aimed to develop and compare improved multiplex conventional and sybr green real time pcr assays for a specific diagnosis of the organisms...

Journal: :molecular and biochemical diagnosis (journal) 2014
seyed hossein mousavi fard shahin merat kiana shahzamani reza ghanbari neda yahoo

background:accumulative research is in progress to clarify clinical aspects of gbv-c. the possibility of interaction between hcv and gbv-c as well as its consequence on development of liver diseases is the most important clinical aspect which encourages researchers to develop a rapid and cost effective technique for simultaneous detection of both viruses.methods: in this study, a sybr green rea...

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