Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes
AUTOR(ES)
Vandesompele, Jo
FONTE
BioMed Central
RESUMO
Using real-time reverse transcription PCR ten housekeeping genes from different abundance and functional classes in various human tissues were evaluated. The conventional use of a single gene for normalization leads to relatively large errors in a significant proportion of samples tested.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=126239Documentos Relacionados
- Improved quantitative real-time RT–PCR for expression profiling of individual cells
- Transcripts of developmentally regulated Plasmodium falciparum genes quantified by real-time RT–PCR
- Quantification of bovine cytokine gene expression using real-time RT-PCR methodology
- A new mathematical model for relative quantification in real-time RT–PCR
- Detecção de Mycobacterium leprae através da técnica de PCR e RT-PCR em tempo real