Cargando…
Faster quantitative real-time PCR protocols may lose sensitivity and show increased variability
Quantitative real-time PCR has become the method of choice for measuring mRNA transcription. Recently, fast PCR protocols have been developed as a means to increase assay throughput. Yet it is unclear whether more rapid cycling conditions preserve the original assay performance characteristics. We c...
Autores principales: | Hilscher, Chelsey, Vahrson, Wolfgang, Dittmer, Dirk P. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2005
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1297710/ https://www.ncbi.nlm.nih.gov/pubmed/16314296 http://dx.doi.org/10.1093/nar/gni181 |
Ejemplares similares
-
Enhanced analysis of real-time PCR data by using a variable efficiency model: FPK-PCR
por: Lievens, Antoon, et al.
Publicado: (2012) -
A new method for robust quantitative and qualitative analysis of real-time PCR
por: Shain, Eric B., et al.
Publicado: (2008) -
Genomic DNA functions as a universal external standard in quantitative real-time PCR
por: Yun, James J., et al.
Publicado: (2006) -
A one-step method for quantitative determination of uracil in DNA by real-time PCR
por: Horváth, András, et al.
Publicado: (2010) -
External oligonucleotide standards enable cross laboratory comparison and exchange of real-time quantitative PCR data
por: Vermeulen, Joëlle, et al.
Publicado: (2009)