A new agarose-based protein electrophoresis gel system is described. T
he system consists of a highly resolving agarose, MetaPhor (R) XR (FMC
BioProducts, Rockland, ME, USA) dissolved in urea and TBE buffer and
a stacking gel composed of a high gel-strength agarose, SeaKem (R) Gol
d (FMC BioProducts). TBE containing sodium dodecyl sulfate (SDS) is us
ed as electrophoresis buffer. The disadvantages of traditional agarose
gels have been overcome, and several advantages over polyacrylamide g
els have been demonstrated. The system is capable of high-resolution s
eparation of small proteins and has a dynamic separation range equival
ent to a 4%-20% gradient polyacrylamide gel. Furthermore, the staining
of protein bands by Coomassie (R) Brilliant Blue is very uniform in t
his gel, and depending on the protein, higher detection sensitivity ca
n be obtained compared to SDS polyacrylamide gels. In Western blotting
, proteins are more efficiently transferred to the membrane from the a
garose gel than from polyacrylamide gels. Finally, the exceptional sta
bility of agarose allows for gels to be precast and stored for a year.