نتایج جستجو برای: real time pcr polymerase chain reaction

تعداد نتایج: 2790868  

2012
Moritz van Vuuren

........................................................................................................................................... IX 1. GENERAL INTRODUCTION .......................................................................................................... 1 2. LITERATURE REVIEW .......................................................................................................

Journal: :jundishapur journal of microbiology 0
than leslie thian lung department of medical microbiology and parasitology, faculty of medicine and health sciences, university putra malaysia, selangor, malaysia chong pei pei department of biomedical sciences, faculty of medicine and health sciences, university putra malaysia, selangor, malaysia ng kee peng department of medical microbiology, faculty of medicine, university of malaya, lumpur, malaysia. seow heng fong department of pathology, faculty of medicine and health sciences, university putra malaysia, selangor, malaysia; department of pathology, faculty of medicine and health sciences, university putra malaysia, seri kembangan, malaysia, malaysia. tel: +60-389464203, fax: +60-389464232

results all eight candida species were successfully detected, identified and quantitated based on the icl gene. a seven-log range of the gene copy number and a minimum detection limit of 103 copies were achieved. conclusions a one-tube absolute quantification real-time pcr that differentiates medically important candida species via individual unique melting temperature was achieved. analytical ...

Journal: :Statistical applications in genetics and molecular biology 2010
Turid Follestad Tommy S Jørstad Sten E Erlandsen Arne K Sandvik Atle M Bones Mette Langaas

We present a Bayesian hierarchical model for quantitative real-time polymerase chain reaction (PCR) data, aiming at relative quantification of DNA copy number in different biological samples. The model is specified in terms of a hidden Markov model for fluorescence intensities measured at successive cycles of the polymerase chain reaction. The efficiency of the reaction is assumed to depend on ...

2012
Antoon Lievens S. Van Aelst M. Van den Bulcke E. Goetghebeur

Current methodology in real-time Polymerase chain reaction (PCR) analysis performs well provided PCR efficiency remains constant over reactions. Yet, small changes in efficiency can lead to large quantification errors. Particularly in biological samples, the possible presence of inhibitors forms a challenge. We present a new approach to single reaction efficiency calculation, called Full Proces...

E. Heidari Arjlo H. Hossainy-Dolatabady M. Muhaghegh-Dolatabady, R. Mahmoudi

Real time-qPCR is the most reliable method for evaluation of mRNA expression levels. However, to obtain accurate results, selection of suitable reference genes is necessary for normalizing the real-time qPCR data. The aim of this research was to validate the expression stability of three potential reference genes (ACTB, GAPDH and UXT) in milk somatic cells of Holstein dairy cattle under differe...

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