نتایج جستجو برای: kit preparation

تعداد نتایج: 203426  

Journal: :The British journal of ophthalmology 2008
P Goldschmidt S Degorge C Saint-Jean H Yera F Zekhnini L Batellier L Laroche C Chaumeil

AIMS Sensitive diagnosis of Acanthamoeba infections may prevent the clinical condition from becoming worse. In order to improve the diagnosis tool performances, we studied the implication of the DNA extraction procedures on the detection of Acanthamoeba by real-time PCR. METHODS Acanthamoeba cysts mixed with a tag virus were processed according to different DNA preparation procedures: heat, P...

2016
Markéta Škereňová Veronika Mikulová Otakar Čapoun Tomáš Zima

INTRODUCTION Nowadays, on-a-chip capillary electrophoresis is a routine method for the detection of PCR fragments. The Agilent 2100 Bioanalyzer was one of the first commercial devices in this field. Our project was designed to study the characteristics of Agilent DNA 1000 kit in PCR fragment analysis as a part of circulating tumour cell (CTC) detection technique. Despite the common use of this ...

Journal: :iranian journal of nuclear medicine 2008
mostafa gandomkar reza najafi mohammad mazidi mostafa goudarzi seyed hassan mirfallah

introduction: ubiquicidin 29-41 (ubi) is a fragment of the cationic antimicrobial peptide that is present in various species including humans. the purpose of this study was to investigate radiochemical and biological characteristics of [6-hydrazinopyridine-3-carboxylic acid (hynic)]-ubi 29-41 designed for the labeling with 99mtc using tricine as coligand. methods: synthesis was preformed on a ...

پایان نامه :وزارت بهداشت، درمان و آموزش پزشکی - دانشگاه علوم پزشکی و خدمات بهداشتی درمانی استان فارس - دانشکده دندانپزشکی 1380

چکیده ندارد.

2015
Nils G. Morgenthaler Markus Kostrzewa

Sepsis is one of the leading causes of deaths, and rapid identification (ID) of blood stream infection is mandatory to perform adequate antibiotic therapy. The advent of MALDI-TOF Mass Spectrometry for the rapid ID of pathogens was a major breakthrough in microbiology. Recently, this method was combined with extraction methods for pathogens directly from positive blood cultures. This review sum...

Journal: :Tropical biomedicine 2011
A A Tan S N Azman N R Abdul Rani B C Kua S Sasidharan L V Kiew N Othman R Noordin Y Chen

There is a great diversity of protein samples types and origins, therefore the optimal procedure for each sample type must be determined empirically. In order to obtain a reproducible and complete sample presentation which view as many proteins as possible on the desired 2DE gel, it is critical to perform additional sample preparation steps to improve the quality of the final results, y...

Journal: :Annals of clinical and laboratory science 2013
Hyunjung Kim Soyoung Shin Eun-Jee Oh Jimin Kahng Yonggoo Kim Hae Kyung Lee Hi Jeong Kwon

BACKGROUND We compared the AdvanSure hepatitis B virus real-time polymerase chain reaction (AdvanSure HBV) kit with three other HBV DNA quantification assays and evaluated its performance. METHODS The AdvanSure HBV real-time PCR assay was compared with the Abbott RealTime HBV Quantification Kit, the COBAS TaqMan HBV Test, and the VERSANT HBV branched DNA 3.0 assay. The precision, linearity, a...

Journal: :Revue scientifique et technique 2014
G K Sharma S Mahajan B Das R Ranjan A Kanani A Sanyal B Pattnaik

Multiplex reverse-transcription polymerase chain reaction (mRT-PCR) assay is a sensitive and rapid method for the detection and serotyping of foot and mouth disease virus (FMDV). However, the method has not been used to its full potential, because of factors such as cost, a lack of infrastructure and the complexity of the reaction mixture. This study was undertaken to optimise and validate a th...

2010
Kirill Gromadski Ruediger Salowsky Susanne Glueck

Next-generation sequencing (NGS) has revolutionized the genetic landscape. It is a lengthy, labor-intensive process that yields results never before achieved. As a result, it is imperative that the quality of the DNA sample be evaluated from the start, as most NGS sample preparation protocols require PCR amplification to generate DNA libraries prior to sequencing. The likelihood of artifact gen...

Journal: :Journal of clinical microbiology 2007
Suzanne M Paule Donna M Hacek Bridget Kufner Karine Truchon Richard B Thomson Karen L Kaul Ari Robicsek Lance R Peterson

We evaluated the use of the BD GeneOhm MRSA real-time PCR assay (BD Diagnostics, San Diego, CA) for the detection of nasal colonization with methicillin-resistant Staphylococcus aureus (MRSA). The initial evaluation consisted of 403 paired nasal swabs and was done using the specimen preparation provided with the kit and an in-house lysis method that was specifically developed to accommodate lar...

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