Northern analysis of bilberry fruit RNA using a non-radioactive detection s
ystem proved to be extremely difficult. To overcome this problem, we used c
DNA instead of RNA for the blotting step. The RNA was translated to cDNA di
rectly after isolation. The cDNA was then separated by electrophoresis, sta
ined with ethidium bromide, and blotted onto a nylon membrane by Southern t
ransfer. Non-radioactive detection by digoxigenin-dUTP was then possible. T
his method resolves several problems associated with northern blotting and
is especially efficient when applied to recalcitrant plant material.