Stellwagen N C
Department of Biochemistry, University of Iowa, Iowa City, USA.
Electrophoresis. 1998 Jul;19(10):1542-7. doi: 10.1002/elps.1150191004.
The electrophoretic mobilities of DNA molecules in three different molecular weight ladders were measured in polyacrylamide gels containing different acrylamide concentrations (%T) and cross-linker ratios (%C), cast and run in Trisacetate-EDTA (TAE) buffer. The apparent pore radius of each gel was estimated from Ferguson plots of the relative mobilities of each of the DNA molecules, using the mobility of the monomer fragment in each molecular weight ladder as the reference mobility. The effective size of each of the DNA molecules was estimated from its radius of gyration. The apparent gel pore radii calculated in this manner ranged from 21 nm in gels containing 10.5%T, 5%C to 200 nm in gels with 4.6%T, 2%C, similar to the values observed for polyacrylamide gels cast and run in Tris-borate-EDTA (TBE) buffer (Holmes and Stellwagen, Electrophoresis 1991, 12, 612-619). Hence, the effective pore size of polyacrylamide gels is essentially independent of whether the gels are cast and run in TAE or TBE buffer.
在含有不同丙烯酰胺浓度(%T)和交联剂比例(%C)的聚丙烯酰胺凝胶中,测量了三种不同分子量梯度的DNA分子的电泳迁移率,这些凝胶在Tris - 乙酸 - 乙二胺四乙酸(TAE)缓冲液中浇铸并运行。使用每个分子量梯度中单体片段的迁移率作为参考迁移率,根据每个DNA分子相对迁移率的弗格森图估算每种凝胶的表观孔径。根据每个DNA分子的回转半径估算其有效大小。以这种方式计算出的表观凝胶孔径范围从含10.5%T、5%C的凝胶中的21纳米到含4.6%T、2%C的凝胶中的200纳米,这与在Tris - 硼酸 - 乙二胺四乙酸(TBE)缓冲液中浇铸并运行的聚丙烯酰胺凝胶所观察到的值相似(霍姆斯和斯特尔瓦根,《电泳》,1991年,第12卷,第612 - 619页)。因此,聚丙烯酰胺凝胶的有效孔径基本上与凝胶是在TAE还是TBE缓冲液中浇铸并运行无关。