Resum
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.
Idioma original | Anglès |
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Pàgines (de-a) | 263-266 |
Revista | Biotechnology Letters |
Volum | 23 |
DOIs | |
Estat de la publicació | Publicada - 28 de febr. 2001 |