نتایج جستجو برای: ژن 16s rrna

تعداد نتایج: 50970  

ژورنال: :iran agricultural research 0
l. lakzadeh shiraz university s. hosseinzadeh shiraz university s.s. shekarforoush shiraz university m. fazeli shiraz university

چکیده- امروزه توجه به تولید محصولات گوشتی بدون تقلب و با هزینه کمتر افزایش یافته است. بنابراین با در نظر گرفتن نگرانی های مربوط به سلامت عمومی اعتقادات مذهبی و مسائل اقتصادی، لازم است اقدامات مناسب جهت ممانعت از این تقلبات به عمل آید. در مطالعه حاضر با استفاده از آزمایش real time pcr به عنوان یک روش سریع، حساس و اختصاصی، به شناسایی و اندازه گیری میزان بافت های مرغی در محصولات گوشتی با برچسب تهی...

Journal: :medical journal of islamic republic of iran 0
salah rahmani dept. of medical biotechnology and the 3 dept. of medical bacteriology, school of medical sciences, tarbiat modarres uniسازمان های دیگر: educational and research center of medical laboratoly sciences, iran university of medical sciences (iums), tehran, iran mehdi forozandeh dept. of medical biotechnology and the 3 dept. of medical bacteriology, school of medical sciences, tarbiat modarres un mirlatif mosavi dept of biology, imam hossein university, tehran,سازمان اصلی تایید شده: دانشگاه تربیت مدرس (tarbiat modares university) abbas rezaee dept. of medical bacteriology, school of medical sciences, tarbiat modarres university, tehran

background: there is a conserved portion in the 16s rrna gene of bacteria which can be amplified by the universal pcr method. this fragment is 996 bp in length. in this method, only one set of universal primers is used for the amplification of the conserved region of the 16s rrna gene, in common bacterial pathogens. therefore, using the universal pcr method, these bacteria are detectable only b...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2012
Verena Salman Rudolf Amann David A Shub Heide N Schulz-Vogt

The gene encoding the small subunit rRNA serves as a prominent tool for the phylogenetic analysis and classification of Bacteria and Archaea owing to its high degree of conservation and its fundamental function in living organisms. Here we show that the 16S rRNA genes of not-yet-cultivated large sulfur bacteria, among them the largest known bacterium Thiomargarita namibiensis, regularly contain...

Journal: :International journal of systematic bacteriology 1998
Z Terefework G Nick S Suomalainen L Paulin K Lindström

PCR-RFLP with nine restriction enzymes was applied to the 16S and 23S rRNA genes of 42 rhizobial and agrobacterial strains to determine the phylogenetic position of Rhizobium galegae and increase the understanding of the evolution of ribosomal operons. The strains were selected based on previous phylogenetic studies. PCR primers were designed so that they amplified a 2.3 kb fragment of the 23S ...

Journal: :Applied and environmental microbiology 2009
Ting Lu Peter G Stroot Daniel B Oerther

Identification and quantification of phylogenetically defined bacterial populations in the environment are often performed using molecular tools targeting 16S rRNA. Fluorescence in situ hybridization has been used to monitor the expression and processing of rRNA by targeting the 3' tail of precursor 16S rRNA. To expand this approach, we employed reverse transcription of total RNA using primer S...

Journal: :Applied and environmental microbiology 2000
J Walter G W Tannock A Tilsala-Timisjarvi S Rodtong D M Loach K Munro T Alatossava

Denaturing gradient gel electrophoresis (DGGE) of DNA fragments obtained by PCR amplification of the V2-V3 region of the 16S rRNA gene was used to detect the presence of Lactobacillus species in the stomach contents of mice. Lactobacillus isolates cultured from human and porcine gastrointestinal samples were identified to the species level by using a combination of DGGE and species-specific PCR...

مقدمه: جنس نوکاردیا جزو اکتینومیست‏های هوازی هستند که یک گروه بزرگ از باکتری‏های ساکن خاک را شامل می‏شوند، که در جهان پخش شده‏اند. در این مطالعه، با استفاده از آزمون‏های تشخیصی رایج، مرسوم و مولکولی گوناگون، چندین ایزوله‏های نوکاردیا جداسازی و تشخیص داده شد. مواد و روش ‏‏ها: در این پژوهش، برای جداسازی از خاک، روش Slip-buried و برای استخراج DNA، روش Microwave oven استفاده شد و در این روش‏ها، سو...

2017
Mabel Sarpong-Duah Michael Frimpong Marcus Beissner Malkin Saar Ken Laing Francisca Sarpong Aloysius Dzigbordi Loglo Kabiru Mohammed Abass Margaret Frempong Fred Stephen Sarfo Gisela Bretzel Mark Wansbrough-Jones Richard Odame Phillips

INTRODUCTION Buruli ulcer (BU) caused by Mycobacterium ulcerans is effectively treated with rifampicin and streptomycin for 8 weeks but some lesions take several months to heal. We have shown previously that some slowly healing lesions contain mycolactone suggesting continuing infection after antibiotic therapy. Now we have determined how rapidly combined M. ulcerans 16S rRNA reverse transcript...

A. R. Jabbari, G. R. Moazeni Jula M. Esmailzadeh M. Moosavi Shoushtari

Pasteurella multocida is known as an important heterogenic bacterial agent causes some severe diseases such as fowl cholera in poultry and haemorrhagic septicaemia in cattle and buffalo. A polymerase chain reaction (PCR) assay was developed using primers derived from conserved part of 16S-23S rRNA gene. The PCR amplified a fragment size of 0.7 kb using DNA from nine avian P. multocida  isolates...

Introduction: Mycoplasmas are one of the most serious contaminants of cellular cultures and their biological productions. Mycoplasma diagnosis is conducted on the basis of culture and molecular methods. These methods are different from each other in terms of accuracy, reliability, and sensitivity. This study aimed to trace the mycoplasma contaminations in culture samples using 16S rRNA specific...

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