For purifying attB-PCR product invitrogen suggests to mix 50µl PCR product+150µl TE buffer+ 100µl 30%PEG8000/30mM MgCl2 solution(provided by invitrogen), vortex & centrifuge at 10000g at RT. Remove supernatant and dissolve the pellet in TE.
It seems its much less laborious than gel elution process.
If somebody is working on this, can you please suggest if it works well?