A series of clones from an Alo-PCR library were analysed in more detai
l. Characterization by Southern blot hybridization and sequencing disp
layed several features common to all probes generated by this approach
: Short length of the PCR-products as well as the presence of homologo
us regions on both ends resulted in a limited feasability for filter h
ybridization and a low probability of restriction length polymorphisms
. In addition, a series of different short repeats at the 3'-ends of A
lu-repeats and present in the generated probes offers a rich source of
potential variable sites accessible by PCR.