نتایج جستجو برای: a 355 bp fragment was amplified from s

تعداد نتایج: 14809709  

Parviz Parvizi, Paul D. Ready,

Phlebotomus papatasi is an important vector of L. major in Iran. P. papatasi was collected from peridomestic animal shelters, inside and around the houses and also the nearby burrows of the gerbil reservoir hosts, Rhombomys opimus, in several provinces in Iran. Mitochondrial Cytochrome b (Cyt b) of sandflies, which is a maternally-inherited gene marker, was used to see if there is any "isolatio...

Scorpion venom is the richest source of peptide toxins with high levels of specific interactions with different ion-channel membrane proteins. The present study involved the amplification and sequencing of a 310-bp cDNA fragment encoding a beta-like neurotoxin active on sodium ion-channel from the venom glands of scorpion Androctonus crassicauda belonging to the Buthidae family using r...

Journal: :avicenna journal of medical biotechnology 0

expressions of recombinant proteins for different applications are important objectives in molecular biotechnology; however, expression of some recombinant proteins is difficult. several methods have been designed for expression of these proteins. the aim of this study was to construct a vector containing mtb32c fragment of mycobacterium tuberculosis (m.tuberculosis) as a fusion partner in orde...

A. R. Jabbari, Gh. R. Moazeni Jula M. Esmaelzadeh

Capsules from a range of pathogenic bacteria are the key determinants of virulency. The capsule hasbeen implicated in virulence of Pasteurella multocida. In this study a type-specific polymerase chain reaction(PCR) assay was used for capsular typing of 39 avian P. multocida isolates from Iran. The PCR amplified afragment of 1044 bp from all of tested isolates. It was found that all avian P. mul...

Journal: :iranian journal of biotechnology 2007
morteza daliri seyed ali ghorashi dina morshedi taraneh hajian kian afshar

a rapid and sensitive reverse transcription polymerase chain reaction (rt-pcr) and nested-pcr were used to detect bovine viral diarrhea virus 1 (bvdv-1) in bull semen. selected primers could amplify a part of the 5´utr of the bvdv genome. a 294 bp dna fragment was amplified and specificity of the results was confirmed by direct sequencing of the pcr product. prior to rna extraction, the seminal...

Journal: :iranian journal of veterinary research 2006
a. r. jabbari m. esmaelzadeh gh. r. moazeni jula

capsules from a range of pathogenic bacteria are the key determinants of virulency. the capsule hasbeen implicated in virulence of pasteurella multocida. in this study a type-specific polymerase chain reaction(pcr) assay was used for capsular typing of 39 avian p. multocida isolates from iran. the pcr amplified afragment of 1044 bp from all of tested isolates. it was found that all avian p. mul...

Journal: :iranian journal of virology 0
a azizi department of plant pathology, tarbiat modares university, tehran, iran m shams-bakhsh department of plant pathology, tarbiat modares university, tehran, iran j mozafari national plant gene bank of iran, seed & plant improvement institute, mahdasht road, karaj, iran r montazeri-hedesh department of plant pathology, tarbiat modares university, tehran, iran

background and aims: tomato yellow leaf curl virus (tylcv) is one of the most destructive viruses of tomato that leads to reduced tomato yield up to 100% in tropical and subtropical regions. in this study, the complete sequence of tylcv isolate from hormozgan province, iran and its recombination evsent was determined. methods: tylcv infected tomato was collected from hormozgan province. total d...

Journal: :iranian journal of veterinary research 2006
m. r. sadeghi s. a. ghorashi r. kargar moakhar d. morshedi r. salehi tabar

marek’s disease (md) is a lymphoproliferative disease of chickens characterized by lymphocyticinfiltration of various organs. the present study was an attempt to use polymerase chain reaction (pcr) tooptimize a rapid and reliable assay for detection of mdv genome. detection of serotype 1 of mdv (mdv-1)was confirmed by presence of a 200 bp dna fragment as a pcr product. differentiation of mdv-1 ...

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: :reports of biochemistry and molecular biology 0
atieh yaghoubi antimicrobial resistance research center, mashhad university of medical sciences, mashhad, iran ehsan aryan antimicrobial resistance research center, mashhad university of medical sciences, mashhad, iran hosna zare antimicrobial resistance research center, mashhad university of medical sciences, mashhad, iran shadi alami antimicrobial resistance research center, mashhad university of medical sciences, mashhad, iran roghayeh teimourpour department of microbiology, school of medicine, ardabil university of medical sciences, ardabil, iran. zahra meshkat tel: +98 51 38012453; fax: +98 51 38002960

background: tuberculosis (tb) is a major cause of death worldwide. finding an effective vaccine against tb is the best way to control it. several vaccines against this disease have been developed but none are completely protective. the aim of this study was to design and construct a cloning vector containing the mycobacterium tuberculosis (m. tuberculosis) heat shock protein x (hspx). methods: ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید