Abstract
The main challenge of RNA extraction from frozen blood samples is to obtain sufficient RNA of acceptable quality for gene expression analysis. In this trial
we compared the RNA stability in clinical blood samples with and without a RNA stabilizer, RNAlater. Results show that high quality RNA can be extracted from blood with RNAlater that has been frozen and thawed several times before the extraction.
we compared the RNA stability in clinical blood samples with and without a RNA stabilizer, RNAlater. Results show that high quality RNA can be extracted from blood with RNAlater that has been frozen and thawed several times before the extraction.
Original language | English |
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Pages | 9 |
Number of pages | 1 |
Publication status | Published - 2011 |
Event | British Toxicology Society Meeting - Nottingham, United Kingdom Duration: 5 Sep 2011 → 6 Sep 2011 |
Conference
Conference | British Toxicology Society Meeting |
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Country/Territory | United Kingdom |
City | Nottingham |
Period | 5/09/11 → 6/09/11 |
Keywords
- genes
- blood cells
- RNA stability
- gene expression analysis