نتایج جستجو برای: quantification pcr

تعداد نتایج: 251724  

2006
K. Nielsen H. S. Mogensen B. Eriksen J. Hedman W. Parson N. Morling

Six commercial preparations of human genomic DNA were quantified using six quantification methods including UV spectrometry, SYBR-green dye staining, slotblot hybridization with the probe D17Z1, and three TaqMan real-time PCR assays: Quantifilerk Human DNA Quantification kit, Quantifilerk Y DNA Quantification kit, and RB1 rt-PCR. In general, all methods measured higher DNA concentrations than e...

Journal: :Journal of clinical microbiology 2004
Petra Wolffs Rickard Knutsson Börje Norling Peter Rådström

The development of real-time PCR thermal cycles in the late 1990s has opened up the possibility of accurate quantification of microorganisms in clinical, environmental, and food samples. However, a lack of suitable sample preparation methods that allow rapid quantification of the nucleic acids, remove PCR inhibitors, and prevent false-positive results due to DNA originating from dead cells has ...

2015
SM Rashed-Ul Islam Munira Jahan Shahina Tabassum

Virological monitoring is the best predictor for the management of chronic hepatitis B virus (HBV) infections. Consequently, it is important to use the most efficient, rapid and cost-effective testing systems for HBV DNA quantification. The present study compared the performance characteristics of a one-step HBV polymerase chain reaction (PCR) vs the two-step HBV PCR method for quantification o...

Journal: :Journal of Japan Society on Water Environment 2011

2010
Da-Sheng Lee

Chip-based DNA quantification systems are widespread, and used in many point-of-care applications. However, instruments for such applications may not be maintained or calibrated regularly. Since machine reliability is a key issue for normal operation, this study presents a system model of the real-time Polymerase Chain Reaction (PCR) machine to analyze the instrument design through numerical ex...

Journal: :Shokuhin eiseigaku zasshi. Journal of the Food Hygienic Society of Japan 2016
Keita Tsukahara Reona Takabatake Tomoko Masubuchi Satoshi Futo Yasutaka Minegishi Akio Noguchi Kazunari Kondo Tomoko Nishimaki-Mogami Takeyo Kurashima Junichi Mano Kazumi Kitta

A real-time PCR-based analytical method was developed for the event-specific quantification of a genetically modified (GM) soybean event, MON87701. First, a standard plasmid for MON87701 quantification was constructed. The conversion factor (Cf) required to calculate the amount of genetically modified organism (GMO) was experimentally determined for a real-time PCR instrument. The determined Cf...

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