Abstract
A rapid and sensitive non-radioactive Northern blot protocol is described which has been optimised in several critical steps. This is based on a formaldehyde-denaturing agarose gel electrophoresis, an alkaline transfer, hybridisation with digoxigenin-DNA probes and detection with a chemiluminescent substrate. This method allows even low abundance mRNAs to be detected in total RNA samples from mammalian tissues.
Original language | English |
---|---|
Pages (from-to) | 263-266 |
Journal | Biotechnology Letters |
Volume | 23 |
DOIs | |
Publication status | Published - 28 Feb 2001 |
Keywords
- Chemiluminescence
- Digoxigenin
- Mammalian tissues
- Non-radioactive
- Northern blot