نتایج جستجو برای: bio pcr

تعداد نتایج: 233744  

2013
Homayoon Bashiri Hamidreza Omrani Masood Mami Mansour Rezaee

BACKGROUND Hepatitis C is one of the common infectious diseases throughout the world. About 170 million people worldwide are infected with Hepatitis C virus. The most common route of transmission is direct blood-to-blood contacts. OBJECTIVES This study conducted to compare the amount of contamination might be found in ultra-filtered liquid passed through 2 kinds of filters ps10 (Mediatex, Ira...

Journal: :The Malaysian journal of pathology 2012
I Latifah M S Rahmat K B Hayarti S Paramasvaran M R Azizah F Imran Y Normaznah

Leptospirosis is an emerging infectious disease. The differential diagnosis of leptospirosis is difficult due to the varied and often "flu like" symptoms which may result in a missed or delayed diagnosis. Leptospira is the aetiological agent of leptospirosis, a bacterial zoonosis with worldwide distribution. There are over 230 known serovars in the genus Leptospira. The true prevalence of lepto...

Journal: :American journal of clinical pathology 2009
Suzanne M Paule Maitry Mehta Donna M Hacek Toni-Marie Gonzalzles Ari Robicsek Lance R Peterson

Surveillance for methicillin-resistant Staphylococcus aureus (MRSA) colonization can be an important element for infection control programs when managing a multidrug-resistant pathogen such as MRSA. The sensitivity and speed of laboratory testing affects the proportion of appropriate isolation days captured, which determines the success or failure of a MRSA control program. Chromogenic culture,...

Journal: :International journal of food microbiology 2004
Samantha Hu Liming Arvind A Bhagwat

An oligonucleotide probe that becomes fluorescent upon hybridization to the target DNA (molecular beacon; MB) was evaluated in a real-time polymerase chain reaction (PCR) assay to detect the presence of Salmonella species. As few as 1-4 colony-forming units (CFU) per PCR reaction could be detected. The capability of the assay to detect Salmonella species from artificially inoculated fresh-cut p...

Journal: :Applied and environmental microbiology 1992
Y L Tsai B H Olson

The polymerase chain reaction (PCR) was used to amplify an Escherichia coli 16S ribosomal gene fragment from sediments with high contents of humic substances. Total DNA was extracted from 1 g of E. coli seeded or unseeded samples by a rapid freeze-and-thaw method. Several approaches (use of Bio-Gel P-6 and P-30 and Sephadex G-50 and G-200 columns, as well as use of the Stoffel fragment) were us...

افشار , پروانه, بذرگر , آزیتا, حاج حیدری , زهره, شکوهی , طاهره, عقیلی , سیدرضا, هاشمی سوته, سیدمحمدباقر, هدایتی , محمدتقی,

Background and Purpose: Lipophilic yeast of the genus Malassezia are members of normal human cutaneous micro flora which are also associated with several skin diseases. It is strongly suspected that Malassezia species are responsible for pityriasis versicolor (PV), and seborrhoeic dermatitis (SD). Considering various sensitivities among Malassezia species to antifungal, accurate species identif...

2016
Jong Eun Park Ji-Youn Kim Sun Ae Yun Myoung-Keun Lee Hee Jae Huh Jong-Won Kim Chang-Seok Ki

Standardized cytomegalovirus (CMV) DNA quantification is important for managing CMV disease. We evaluated the performance of the Real-Q CMV Quantification Kit (Real-Q assay; BioSewoom, Korea) using whole blood (WB), with nucleic acid extraction using MagNA Pure 96 (Roche Diagnostics, Germany). Real-time PCR was performed on two platforms: the 7500 Fast real-time PCR (7500 Fast; Applied Biosyste...

Journal: :Journal of microbiological methods 2008
Elisabeth Fredlund Ann Gidlund Monica Olsen Thomas Börjesson Niels Henrik Hytte Spliid Magnus Simonsson

Identification of Fusarium species by traditional methods requires specific skill and experience and there is an increased interest for new molecular methods for identification and quantification of Fusarium from food and feed samples. Real-time PCR with probe technology (Taqman) can be used for the identification and quantification of several species of Fusarium from cereal grain samples. Ther...

1999
Brian C. Schutte Koustubh Ranade Jonathan Pruessner

1.Atcheson, C.L., B. DiDomenico, S. Frackman, R.E. Esposito and R.T. Elder. 1987. Isolation, DNA sequence, and regulation of a meiosis-specific eukaryotic recombination gene. Proc. Natl. Acad. Sci. USA 84:80358039. 2.Cha, J., W. Bishai and S. Chandrasegaran. 1993. New vectors for direct cloning of PCR products [published erratum appears in Gene 1994; 141:149]. Gene 136:369-370. 3.Clark, J.M. 19...

2004
S. H. LIMING Y. ZHANG J. MENG A. A. BHAGWAT

The capability of an assay to detect Listeria monocytogenes from artificially inoculated fresh-cut produce such as cantaloupe and mixed salad was demonstrated. An oligonucleotide probe that becomes fluorescent upon hybridization to the target DNA (Molecular Beacon, MB) was used in a real-time polymerase chain reaction (PCR) assay. As few as 4 to 7 colony-forming units (CFU) of L. monocytogenes ...

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