The detection of the genetic modification in silage obtained from insect-re
sistant Bt maize by means of the polymerase chain reaction (PCR) is describ
ed. The detectability of the transgene was shown to be dependent on the len
gth of the genomic target sequence chosen for amplication by the PCR. By am
plifying a Bt-maize-specific DNA sequence of 211 bp the genetic modificatio
n was detected up to 7 months after ensilage. The effect of maize DNA degra
dation in the course of the ensilage on the detectability of target sequenc
es was demonstrated in model experiments.