نتایج جستجو برای: pcr gene detection

تعداد نتایج: 1737497  

Journal: :journal of cell and molecular research 0
seyed ali mortazavi ahmad reza bahrami balal sadeghi maryam moghaddam matin

in present study, a sybr green based real time pcr assay was developed for specific detection and quantification of bacillus subtilis in dough used for bread making. new primer pairs were designed to amplify a 212 base pair fragment of the apre gene. specificity of these primer pairs was confirmed with conventional and real time pcr methods. standard curves constructed using the threshold cycle...

2017
Paul T. Odinot

Objectives: Detection of Yersinia enterocolitica in clinical samples is still not sensitive and fast enough. Polymerase chain reaction (PCR) offers the advantages of sensitivity, specificity, and rapidity. A two-step PCR assay to detect pathogenic Y: enterocolitica in infected tissue has been developed. Method: In the first step of the PCR assay, a general primer PCR amplification of the small ...

Journal: :iranian journal of medical sciences 0
a. zahedmehr department of biotechnology, pas-teur institute of iran, tehran, iran s. delmaghani department of biotechnology, pas-teur institute of iran, tehran, iran r. sharifian hemophilia centre, imam khomeini hospital, tehran university of medical sciences, tehran, iran m. lak hemophilia centre, imam khomeini hospital, tehran university of medical sciences, tehran, iran s. zeinali department of biotechnology, pas-teur institute of iran, tehran, iran

background: hemophilia b is an x-linked recessive coagulation disorder caused by factor ix deficiency.  analysis of factor ix gene polymorphisms is considered the best approach for prenatal diagnosis and carrier detection of hemophilia b where the identification of gene mutation is not easily possible.   objective: to study the frequency of three factor ix-linked restriction fragment length pol...

Hadi Shirzad Hourieh Saderi Majid Sadeghizadeh, Mehrdad Behmanesh, Narges Kharazani Tafreshi Roohollah Nakhaei Sistani

Adenoviruses (AdVs) types 40 and 41 are the causative agents of diarrhea in children. Hence, rapid sensitive and specific detection of these viruses are of clinical importance. The customary methods such as propagation of virus in cell culture suffer from limitations. Detection of immobilized amplified products in a one phase system (DIAPOPS) method has the potential to overcome these problems....

Journal: :iranian journal of basic medical sciences 0
maryam fazelzadeh haghighi cancer immunology group, shiraz institute for cancer research, school of medicine, shiraz university of medical sciences, shiraz, iran mohammad ali ghayumi department of internal medicine, school of medicine, shiraz university of medical sciences, shiraz, iran farzane behzadnia cancer immunology group, shiraz institute for cancer research, school of medicine, shiraz university of medical sciences, shiraz, iran nasrollah erfani molecular medicine group, graduate school of advanced medical sciences and technologies, shiraz university of medical sciences, shiraz, iran

objective(s): foxp3 gene is an x-linked gene that encodes foxp3 protein, an essential transcription factor in cd4+cd25+foxp3+ regulatory t (treg) cells.  we aimed, in the present study, to investigate the association of two foxp3 polymorphisms, -2383 c/t (rs3761549) and ivs9+459 t/c (rs2280883), with lung cancer. materials and methods:  in a case-control study we analyzed genotypes and alleles ...

Journal: :Clinical chemistry 2015
Elena Castellanos-Rizaldos Katherine Richardson Rui Lin Grant Wu Mike G Makrigiorgos

BACKGROUND Multiplexed detection of low-level mutations presents a technical challenge for many technologies, including cancer gene panels used for targeted-resequencing. Analysis of mutations below approximately 2%-5% abundance in tumors with heterogeneity, samples with stromal contamination, or biofluids is problematic owing to increased noise from sequencing errors. Technologies that reduce ...

Journal: :iranian journal of parasitology 0
m niyyati j lorenzo-morales m mohebali s rezaie f rahimi z babaei

background: the aim was to compare three different methods (direct examination, culture and pcr meth­ods) for the diagnosis of acanthamoeba keratitis (ak) in corneal scrapes. methods: twenty eight corneal scrapes and contact lenses were collected from keratitis patients and re­ferred to the de­partment of medical parasitology and mycology, school of public health, tehran univer­sity of medical ...

Journal: :iranian journal of applied animal science 2014
a. zakeri

the aim of this study was to isolate escherichia coli from chickens and to determine the presence of the eaea gene, a virulence factor detected in escherichia coli, in the isolates by polymerase chain reaction (pcr). different chicken organs (lung, liver and spleen) were inoculated onto blood agar and biochemical tests were performed on the suspicious isolates. escherichiacoliwas isolated from ...

Journal: :iranian journal of microbiology 0
m soltani department of aquatic animal health, faculty of veterinary medicine, university of tehran, tehran, iran. e pirali department of aquatic animal health, faculty of veterinary medicine, university of tehran, tehran, iran. p shayan department of parasitology, faculty of veterinary medicine, university of tehran, tehran, iran. b eckert investigation institute of molecular biology and system transfer (mbst), tehran, iran. s rouholahi department of aquatic animal health, faculty of veterinary medicine, university of tehran, tehran, iran. n sadr-shirazi investigation institute of molecular biology and system transfer (mbst), tehran, iran.

background and objective: streptococcosis/lactococcosis is the cause of high morbidity and mortality in aquaculture sector and to date a number of species of streptococcus and lactococcus genera including s. iniae, s. agalactiae, s. dysagalactiae, s. parauberis, s. feacalis, l. garvieae and l. lactis have been discriminated as the cause of disease in aquatic animals. despite the use of diagnost...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تبریز - دانشکده مهندسی برق و کامپیوتر 1393

در این پروژه هدف طراحی و ساخت fluorescence detection systemجهت آشکارسازی مولکول های dna می باشد. در روش pcr، طی چندین چرخه دمایی، مولکول های dna کپی می شوند و سپس با استفاده از روش fluorescence detection، مولکول های بر انگیخته شده dna آشکارسازی می شوند. پس از آشکارسازی می توان به کپی و یا عدم کپی dnaها پی برد.می توان برای جداسازی مولکول های dna بر اساس طولشان، از روش gel electrophoresis استفاده...

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