نتایج جستجو برای: quantitative rt

تعداد نتایج: 366631  

Journal: :BioTechniques 2003
Mary Lynn Johnson Chainarong Navanukraw Anna T Grazul-Bilska Lawrence P Reynolds Dale A Redmer

Vol. 35, No. 6 (2003) BioTechniques 1141 the ABI PRISM® 7000 and the TaqMan Universal PCR Master Mix protocols (Applied Biosystems). After discovering that the RNA from the thecal cells had vascular endothelial growth factor (VEGF) amplification and that RNA from granulosa cells had no VEGF amplification, the 18S rRNA amplification (TaqMan Pre-Developed Assay Reagents; Applied Biosystems), whic...

Journal: :BioTechniques 1997
D Mitra J Laurence

3.Higuchi, R., B. Krummel and R.K. Saiki. 1988. A general method of in vitro preparation and specific mutagenesis of DNA fragments: study of protein and DNA interactions. Nucleic Acids Res. 16:7351-7367. 4.Sarkar, G. and S.S. Sommer. 1990. The “megaprimer” method of site-directed mutagenesis. BioTechniques 8:404-407. 5.Smith, M. 1985. In vitro mutagenesis. Annu. Rev. Genet. 19:423-462. 6.Upende...

Journal: :Bioinformatics 2003
Perikles Simon

SUMMARY Q-Gene is an application for the processing of quantitative real-time RT-PCR data. It offers the user the possibility to freely choose between two principally different procedures to calculate normalized gene expressions as either means of Normalized Expressions or Mean Normalized Expressions. In this contribution it will be shown that the calculation of Mean Normalized Expressions has ...

2005
S A Bustin M W Pfaffl

The real-time reverse transcription polymerase chain reaction (RT-PCR) uses fluorescent reporter molecules to monitor the production of amplification products during each cycle of the PCR reaction. This combines the nucleic acid amplification and detection steps into one homogeneous assay and obviates the need for gel electrophoresis to detect amplification products. Use of appropriate chemistr...

Journal: :BioTechniques 2000
S Raja J D Luketich L A Kelly D W Ruff T E Godfrey

With the introduction of real-time, fluorescence-based 5′ nuclease PCR (3,4) and instruments such as the ABI PRISM 7700 (TaqMan) sequence detector (Applied Biosystems, Foster City, CA, USA), quantitative RT-PCR is now a widely accepted method for measuring gene expression levels. Quantitative RTPCR is a sensitive technique and is particularly useful for the analysis of samples containing limi...

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