Cargando…
An Extended ΔCT-Method Facilitating Normalisation with Multiple Reference Genes Suited for Quantitative RT-PCR Analyses of Human Hepatocyte-Like Cells
Reference genes (RG) as sample internal controls for gene transcript level analyses by quantitative RT-PCR (RT-qPCR) must be stably expressed within the experimental range. A variety of in vitro cell culture settings with primary human hepatocytes, and Huh-7 and HepG2 cell lines, were used to determ...
Autores principales: | Riedel, Gesa, Rüdrich, Urda, Fekete-Drimusz, Nora, Manns, Michael P., Vondran, Florian W. R., Bock, Michael |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3962476/ https://www.ncbi.nlm.nih.gov/pubmed/24658132 http://dx.doi.org/10.1371/journal.pone.0093031 |
Ejemplares similares
-
Identification of reference genes for RT-qPCR data normalisation in aging studies
por: González-Bermúdez, Lourdes, et al.
Publicado: (2019) -
Reference gene identification for reliable normalisation of quantitative RT-PCR data in Setaria viridis
por: Nguyen, Duc Quan, et al.
Publicado: (2018) -
ReadqPCR and NormqPCR: R packages for the reading, quality checking and normalisation of RT-qPCR quantification cycle (Cq) data
por: Perkins, James R, et al.
Publicado: (2012) -
CD4 and CD8 T lymphocyte interplay in controlling tumor growth
por: Ostroumov, Dmitrij, et al.
Publicado: (2017) -
Selection of reference genes for normalisation of real-time RT-PCR in brain-stem death injury in Ovis aries
por: Passmore, Margaret, et al.
Publicado: (2009)