A uridine-based linker immobilized onto polystyrene beads at the 5' terminu
s via a phosphodiester group and then used as a universal DNA synthesis sup
port gives post synthesis DNA cleavage in 8 hrs or less without alkali meta
l salts. DNA produced with the new support was analyzed by HPLC, MALDI mass
spectroscopy and PAGE. Each analysis showed DNA of equivalent quality to t
hat produced with standard CPG supports, without contaminating materials re
sulting from linker or support backbone decomposition.