نتایج جستجو برای: dna extraction

تعداد نتایج: 663961  

Journal: :Molecular and cellular probes 2006
Leslie Cler Dawei Bu Cheryl Lewis David Euhus

Translational protocols in cancer and carcinogenesis often require isolation of genomic DNA from paucicellular clinical samples. DNA extraction methods for PCR-based applications should optimize the recovery of amplifiable DNA. We compared five methods for DNA extraction in paucicellular epithelial and lymphocyte samples using proportion of extractions producing amplifiable DNA and mean real-ti...

2017
Lilit Atanesyan Maryvonne J. Steenkamer Anja Horstman Cathy B. Moelans Jan P. Schouten Suvi P. Savola

Objectives Molecular genetic analysis of formalin-fixed, paraffin-embedded (FFPE) tissues is of great importance both for research and diagnostics. Multiplex ligation-dependent probe amplification (MLPA) is a widely used technique for gene copy number determination, and it has been successfully used for FFPE tissue-extracted DNA analysis. However, there have been no studies addressing the effec...

2017
Per Eriksson Evangelos Mourkas Daniel González-Acuna Björn Olsen Patrik Ellström

Introduction: Advances in the development of nucleic acid-based methods have dramatically facilitated studies of host-microbial interactions. Fecal DNA analysis can provide information about the host's microbiota and gastrointestinal pathogen burden. Numerous studies have been conducted in mammals, yet birds are less well studied. Avian fecal DNA extraction has proved challenging, partly due to...

Journal: :iranian red crescent medical journal 0
mahsa tabibnejad department of immunology and microbiology, arak university of medical sciences, arak, ir iran mohammad yousef alikhani brucellosis research center, hamadan university of medical sciences, hamadan, ir iran; brucellosis research center, hamadan university of medical sciences, hamadan, ir iran. tel: +98-9125443147, fax: +98-8132533936, e-mail:; mohammad arjomandzadegan, tuberculosis and pediatric infectious research center and department of microbiology, arak university of medical sciences, arak, ir iran. tel: +98-9188602576, fax: +98-8634173518 mohammad arjomandzadegan tuberculosis and pediatric infectious research center and department of microbiology, arak university of medical sciences, arak, ir iran; brucellosis research center, hamadan university of medical sciences, hamadan, ir iran. tel: +98-9125443147, fax: +98-8132533936, e-mail:; mohammad arjomandzadegan, tuberculosis and pediatric infectious research center and department of microbiology, arak university of medical sciences, arak, ir iran. tel: +98-9188602576, fax: +98-8634173518 seyed hamid hashemi brucellosis research center, hamadan university of medical sciences, hamadan, ir iran zahra naseri blood transfusion research center, high institute for research and education in transfusion, hamadan, ir iran

conclusions the results prove that the presented double pcr method could be used to detect positive cases from culture-negative blood samples. the chelex 100 method is simpler and safer than the use of qiagen kit for dna extraction. materials and methods a total of 100 patients with suspected brucellosis were included in this experimental study and given positive serological tests. diagnosis wa...

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