نتایج جستجو برای: using a universal primers set

تعداد نتایج: 14130021  

R. MOSTOWFIZADEH-GHALAMFARSA S. JAMALI Z. BANIHASHEMI

ABSTRACT- Desert truffles are hypogeous ascomyceteous ectomycorrhizal fungi, occurring in arid and semi-arid ecosystems. A PCR-based method was developed for the identification of 3 major desert truffles of Iran: Terfezia claveryi, Tirmania pinoyi and Tirmania nivea based on internal transcribed spacers of rDNA. Two specific PCR primers were designed for T. claveryi, 4 for T. pinoyi, and 2 for ...

Journal: :iran agricultural research 2014
r. mostowfizadeh-ghalamfarsa z. banihashemi s. jamali

abstract- desert truffles are hypogeous ascomyceteous ectomycorrhizal fungi, occurring in arid and semi-arid ecosystems. a pcr-based method was developed for the identification of 3 major desert truffles of iran: terfezia claveryi, tirmania pinoyi and tirmania nivea based on internal transcribed spacers of rdna. two specific pcr primers were designed for t. claveryi, 4 for t. pinoyi, and 2 for ...

Journal: :تحقیقات دامپزشکی 0
مهدی وجگانی گروه علوم درمانگاهی دانشکده دامپزشکی دانشگاه تهران سید مصطفی پیغمبری گروه علوم درمانگاهی دانشکده دامپزشکی دانشگاه تهران حسن حکیمی گروه علوم درمانگاهی دانشکده دامپزشکی دانشگاه تهران

this study was conducted to detect the common bacteria implicated in bovine mastitis in bulk tank milk by polymerase chain reaction (pcr). forty-four milk samples from bulk tank milk were obtained and submitted to our laboratory. to detect staphylococcus aureus, streptococcus agalactiae, streptococcus dysgalactiae, escherichia coli, streptococcus uberis, and streptococcus parauberis, two sets o...

ABBAS REZAEE, MEHDI FOROZANDEH, MIRLATIF MOSAVI, SALAH RAHMANI,

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 on...

A. Akhondzadeh Basti, A. Misaghi, D. Al-taghlubee, D. Shayan, H. Gandomi, P. Shayan,

Background: Meat species adulteration has become a problem of concern. This study aimed to compare two previously published multiplex Polymerase Chain Reaction (PCR) methods for meat species authentication.  Methods: The primers used in the first multiplex PCR involved species-specific reverse primer for sheep, goat, cattle, pig, and donkey with universal forward primer. In the second multiple...

Journal: :مجله میکروب شناسی پزشکی ایران 0
هومن صدیقیان homan sedghian urology research center, sina hospital, tehran university of medical sciencesبخش میکروب شناسی، گروه پاتوبیولوژی، دانشکده بهداشت، دانشگاه علوم پزشکی تهران محمدرضا پورمند mohammadreza pourmand department of pathobiology, school of public health, tehran university of medical sciencesبخش میکروب شناسی، گروه پاتوبیولوژی، دانشکده بهداشت، دانشگاه علوم پزشکی تهران

background and objectives: urinary tract infection (uti) is one of the most common infections and a major cause of patient morbidity world wide. the gold standard for detection of bacterial pathogens in uti is culture of urine specimens. in order to facilitate identification of bacterial pathogens in clinical urine specimens we designed a molecular method to detect bacterial pathogen in uti. ma...

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...

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