نتایج جستجو برای: sarcocystis gigantea wasidentified by amplification of 18s rrna gene using pcr

تعداد نتایج: 21962577  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه صنعتی اصفهان - دانشکده کشاورزی 1393

سیب زمینی با نام علمی (solanum tuberosum l.)، از نظر اهمیت غذایی و اقتصادی بعد از محصولاتی چون گندم، برنج، ذرت و جو در رتبه پنجم قرار دارد. بیماری های ویروسی از مهم ترین عوامل خسارت زای سیب زمینی در جهان و ایران محسوب می شوند. ویروس های آلوده کننده سیب زمینی از جمله ویروس وای سیب زمینی، پیچیدگی برگ سیب زمینی ، اس سیب زمینی و موزاییک یونجه در مناطق مهم سیب زمینی کاری دنیا، خسارات شدید اقتصادی را...

ژورنال: علوم آب و خاک 2009
بهار, مسعود, سعیدی, قدرت اله, طالبی بداف, مجید, محمدی, سید ابوالقاسم,

To characterize the geographical distribution of medicago-nodulating rhizobia in western regions of Iran, 950 Sinorhizobium isolates were trapped from a combination of two local alfalfa populations (Hamedani, Nikshahri) together with a foreign cultivar ( Kodi) and soil samples from eight sites across Kurdestan, Kermanshah, Eastern Azarbayjan and Lorestan provinces. Also, a total of 45 isolates ...

Journal: :research in molecular medicine 0
zohreh hojati genetics division, biology department, faculty of sciences, university of isfahan, isfahan, iran zeinab hallajian genetics division, biology department, faculty of sciences, university of isfahan, isfahan, iran abolghasem esmaeili genetics division, biology department, faculty of sciences, university of isfahan, isfahan, iran majid motovali-bashi genetics division, biology department, faculty of sciences, university of isfahan, isfahan, iran hosein tabatabaeian genetics division, biology department, faculty of sciences, university of isfahan, isfahan, iran

background: amplification of her2 is seen in 20-30% of breast cancer cases. measurement of her2 gene amplification appears to be of vital importance in planning the treatment schedule for patients with breast carcinoma. the aim of our study was to evaluate her2 amplification status in malignant and benign breast tumors by differential pcr (dpcr). materials and methods: the genomic dna was extra...

2011
Annetta Zintl Eugene J Finnerty Thomas M Murphy Theo de Waal Jeremy S Gray

Blood samples were obtained from 38 wild red deer (Cervus elaphus) at two sites in Ireland and subjected to PCR analysis of the 18S rRNA gene followed by sequencing. Two fragments of the 18S rRNA gene were generated by two different PCR protocols and subsequent sequencing suggested that at least six of the deer were infected by a babesia that, in those loci, is indistinguishable from Babesia di...

بهار, مسعود, سعیدی, قدرت اله, طالبی بداف, مجید, محمدی, سید ابوالقاسم,

To characterize the geographical distribution of medicago-nodulating rhizobia in western regions of Iran, 950 Sinorhizobium isolates were trapped from a combination of two local alfalfa populations (Hamedani, Nikshahri) together with a foreign cultivar ( Kodi) and soil samples from eight sites across Kurdestan, Kermanshah, Eastern Azarbayjan and Lorestan provinces. Also, a total of 45 isolates ...

Journal: :iranian journal of veterinary research 2007
a. jamshidi d. j. hampson

avian intestinal spirochaetosis (ais) is a condition arising from colonization of the caeca and colon of birds with anaerobic spirochaetes of the genus brchyspira. the purpose of the present study was to evaluate pcr amplification from formalin-fixed, paraffin-embedded tissue method for detecting infected laying hens with brachyspira pilosicoli  with the same primers that have been used for det...

Hepatozoon species are protozoan parasites that infect some animals such as birds, reptiles, amphibians, and carnivores. Previous studies performed on canine hepatozoonosis in Iran have never used molecular techniques for diagnosis of this disease. The main objective of the present study was to detect Hepatozoon canis in the blood of dogs using polymerase chain reaction (PCR) method and sequenc...

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: :Applied and environmental microbiology 2008
Cécile Lepère Isabelle Domaizon Didier Debroas

The diversity of small eukaryotes (0.2 to 5 mum) in a mesotrophic lake (Lake Bourget) was investigated using 18S rRNA gene library construction and fluorescent in situ hybridization coupled with tyramide signal amplification (TSA-FISH). Samples collected from the epilimnion on two dates were used to extend a data set previously obtained using similar approaches for lakes with a range of trophic...

Journal: :Journal of clinical microbiology 2003
Wangeci Gatei Julie Greensill Richard W Ashford Luis E Cuevas Christopher M Parry Nigel A Cunliffe Nicholas J Beeching C Anthony Hart

An 840-bp fragment of the 18S rRNA gene was used to identify Cryptosporidium spp. recovered from human immunodeficiency virus (HIV)-infected and -uninfected patients from Kenya, Malawi, Brazil, the United Kingdom, and Vietnam. Initial identification was by Ziehl-Neelsen acid-fast staining. Confirmation was by nested PCR, targeting the most polymorphic region of the 18S rRNA gene. Genotyping was...

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