Tris-Acetate/SDS running buffer is used to resolve high molecular weight proteins (36-400 kDa) under denaturing conditions on Tris/Acetate gels
仕様
Tris-Acetate/SDS running buffer is compatible with Tris/Acetate gels
Separate high molecular weight proteins (36-400 kDa) under denaturing conditions on Tris/Acetate gels.
Tris-Acetate system operates at significantly lower operating pH of 8.1 during electrophoresis when compared to traditional LaemmLi system thus enabling better band resolution
Tris-Acetate/SDS running buffer [1X] pH is 8.2
1 X concentarion:50 mM Tricine, 50 mM Tris Base, 0.1% SDS