• Medientyp: E-Artikel
  • Titel: The 'PREXCEL-Q Method' for qPCR
  • Beteiligte: Gallup, Jack M.; Ackermann, Mark R.
  • Erschienen: International Assotiation of Biomedical Sciences, 2008
  • Erschienen in: International Journal of Biomedical Science
  • Sprache: Nicht zu entscheiden
  • DOI: 10.59566/ijbs.2008.4273
  • ISSN: 1555-2810; 1550-9702
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: <jats:p>The purpose of this manuscript is to describe a reliable approach to quantitative real-time polymerase chain reaction (qPCR) assay development and project management, which is currently embodied in the Excel 2003-based software program named 'PREXCEL-Q' (P-Q) (formerly known as 'FocusField2-6Gallup-qPCRSet-upTool-001,' 'FF2-6-001 qPCR set-up tool' or 'Iowa State University Research Foundation [ISURF] project #03407'). Since its inception from 1997-2007, the program has been well-received and requested around the world and was recently unveiled by its inventor at the 2008 Cambridge Healthtech Institute's Fourth Annual qPCR Conference in San Diego, CA. P-Q was subsequently mentioned in a review article by Stephen A. Bustin, an acknowledged leader in the qPCR field. Due to its success and growing popularity, and the fact that P-Q introduces a unique/defined approach to qPCR, a concise description of what the program is and what it does has become important. Sample-related inhibitory problems of the qPCR assay, sample concentration limitations, nuclease-treatment, reverse transcription (RT) and master mix formulations are all addressed by the program, enabling investigators to quickly, consistently and confidently design uninhibited, dynamically-sound, LOG-linear-amplification-capable, high-efficiency-of-amplification reactions for any type of qPCR. The current version of the program can handle an infinite number of samples.</jats:p>
  • Zugangsstatus: Freier Zugang