نتایج جستجو برای: multiplex pcr

تعداد نتایج: 186945  

ژورنال: :مجله طب نظامی 0
بابک براتی barati b. گروه علوم زیستی، دانشگاه امام حسین(ع)، تهران، ایران مجتبی سعادتی saadati m. گروه علوم زیستی، دانشگاه امام حسین(ع)، تهران، ایرانسازمان اصلی تایید شده: دانشگاه جامع امام حسین (imam hosseyn university) میرزاخلیل بهمنی bahmani m. kh. گروه علوم زیستی، دانشگاه امام حسین(ع)، تهران، ایرانسازمان اصلی تایید شده: دانشگاه جامع امام حسین (imam hosseyn university)

[-1] (pcr ] می توان حضور سویه های استافیلوکوکوس اورئوس انتروتوکسوژنیک را قبل از بیان انتروتوکسین و بر اساس توالی اختصاصی ژن نشان داد. مواد و روش  کار. در این مطالعه سویه های استافیلوکوکوس اورئوس جداسازی شده از نمونه های بیماران، ناقلین سالم و محیطی با آزمایش های بیوشیمیایی شناسایی شدند. سپس نسبت به طراحی پرایمرهای مورد نظر اقدام و در واکنش pcr ، ژن انتروتوکسین استافیلوکوکی تایپ a ( sea ) و ژن ن...

2011
Farah Al-Marzooq

Establishing a microbial diagnosis for patients with community-acquired pneumonia (CAP) is still challenging and is often achieved in only 30-50% of cases. Polymerase chain reaction (PCR) has been shown to be more sensitive than conventional microbiological methods and it could help to increase the microbial yield for CAP patients. This study was designed to develop, optimize and evaluate multi...

2016
Jacqueline Heckenhauer Michael H. J. Barfuss Rosabelle Samuel

PREMISE OF THE STUDY PCR amplification of the matK barcoding region is often difficult when dealing with multiple angiosperm families. We developed a primer cocktail to amplify this region efficiently across angiosperm diversity. METHODS AND RESULTS We developed 14 matK primers (seven forward, seven reverse) for multiplex PCR, using sequences available in GenBank for 178 taxa belonging to 123...

Journal: :Expert Review of Anti-infective Therapy 2010

Journal: :Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi 2013
Yu-Shen Chen Po-Yen Liu Yung-Feng Huang Chiao-Shan Chen Ling-Hui Chiu Nuan-Ya Huang Kai-Sheng Hsieh Yao-Shen Chen

BACKGROUND/PURPOSE Acute respiratory tract infections are a leading cause of morbidity and mortality in children worldwide. Most have a viral etiology, with pneumococcus as an important pathogen. This single-center study compared the use of conventional diagnostic tools and two multiplex polymerase chain reaction (PCR) examinations for determining pathogens in lower respiratory tract infections...

2017
C. Latha C. J. Anu V. J. Ajaykumar B. Sunil

AIM The objective of the study was to investigate the occurrence of Listeria monocytogenes, Yersinia enterocolitica, Staphylococcusaureus, and Salmonella enterica Typhimurium in meat and meat products using the multiplex polymerase chain reaction (PCR) method. MATERIALS AND METHODS The assay combined an enrichment step in tryptic soy broth with yeast extract formulated for the simultaneous gr...

2016
Reza Ranjbar Ali Naghoni Davoud Afshar Farhad Nikkhahi Mohsen Mohammadi

OBJECTIVES Gastrointestinal tract infection is still one of the serious public health problems in many geographic areas and is endemic in most countries including Iran. Early detection of the gastrointestinal tract pathogens can be extremely important. The aim of the current study was to apply a shortened time-multiplex polymerase chain reaction (PCR) for rapid and simultaneous detection of Sal...

Journal: :The Malaysian journal of pathology 2012
Norazah Ahmad Shirley Tang Gee Hoon Mohamed Kamel Abd Ghani Koh Yin Tee

Serotyping is not sufficient to differentiate between Salmonella species that cause paratyphoid fever from the strains that cause milder gastroenteritis as these organisms share the same serotype Salmonella Paratyphi B (S. Paratyphi B). Strains causing paratyphoid fever do not ferment d-tartrate and this key feature was used in this study to determine the prevalence of these strains among the c...

Journal: :Journal of clinical microbiology 2002
Guizhen Luo Thomas G Mitchell

A multiplex PCR method was developed to identify simultaneously multiple fungal pathogens in a single reaction. Five sets of species-specific primers were designed from the internal transcribed spacer (ITS) regions, ITS1 and ITS2, of the rRNA gene to identify Candida albicans, Candida glabrata, Candida parapsilosis, Candida tropicalis, and Aspergillus fumigatus. Another set of previously publis...

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