Stabilized polyacrylamide gels and system for SDS electrophoresis

Claim 2

A buffer system for conducting discontinuous sodium dodecyl sulfate polyacrylamide gel electrophoresis, comprising (a) a stabilized polyacrylamide gel medium containing a gel buffer of a salt of 2-amino-2-methyl-1,3-propanediol at a pH of about 6.4 to 7.3, and (b) 2-amino-2-methyl-1,3-propanediol taurine, at a pH of about 8.0 to 10.0 as an elctrolyte buffer.

Claim 3

A buffer system as claimed in claim 1 wherein the 2-amino-2-methyl-1,3-propanediol has a pH of about 6.8 to 7.1.

Claim 4

A buffer system as claimed in claim 1 wherein the gel buffer is selected from the group consisting of 2-amino-2-methyl-1,3-propanediol chloride, sulfate, nitrite and fluoride.

Claim 5

A buffer system as claimed in claim 3 wherein the gel buffer is 2-amino-2-methyl-1,3-propanediol chloride or sulfate.

Claim 6

In a discontinuous sodium dodecyl sulfate polyacrylamide gel electrophoresis process for determining the molecular weight of a macromolecule which includes the steps of mixing the macromolecules with sodium dodecyl sulfate, adding the mixture to a polyacrylamide gel medium containing acrylamide monomers in a gel buffer, placing the gel medium in contact with an ioncontaining electrolyte solution, subjecting the macromolecules and gel medium to a differential electrical potential to produce migration of the macromolecules and electrolyte ions and determining the molecular weight of said macromolecule, the improvement which comprises using as the gel buffer a salt of 2-amino-2-methyl-1,3-propanediol at a pH of about 6.4 to 7.3 and using as an electrolyte buffer 2-amino-2-methyl-1,3-propanediol taurine at a pH of about 8.0 to 10.0.

Claim 7

In a discontinuous sodium dodecyl sulfate polyacrylamide gel electrophoresis process for determining the molecular weight of a macromolecule which includes the steps of mixing the macromolecules with sodium dodecyl sulfate, adding the mixture to a polyacrylamide gel medium containing acrylamide monomers in a gel buffer, placing the gel medium in contact with an ioncontaining electrolyte solution, subjecting the macromolecules and gel medium to a differential electrical potential to produce migration of the macromolecules and electrolyte ions and determining the molecular weight of said macromolecule, the improvement which comprises using as the gel buffer a salt of 2-amino-2-methyl-1,3-propanediol at a pH of about 6.4 to 7.3 and using as an electrolyte buffer 2-amino-2-methyl-1,3-propanediol taurine at a pH of about 8.0 to 10.0.