Electrophoretic resolution of single strand DNA by asymmetric field inversion
AssigneeThe University of North Carolina at Chapel Hill
InventorEric Lai
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Abstract
Single stranded DNA fragments in sizes above 300 bases are separated electrophoretically in a field inversion technique in which the voltage of the reverse pulse exceeds that of the forward pulse, the duration of the forward pulse exceeds that of the reverse pulse, and the product of voltage and duration for the forward pulse exceeds that of the reverse pulse. The result is an improvement in resolution over previous field inversion techniques, and the elimination of band inversion.
Claims11
A method for the electrophoretic separation of a mixture of single strand DNA molecules of 200 or more bases in length along a preselected direction of migration in an electrophoretic separation medium, said method comprising imposing across said medium electrical fields alternating between a forward field and a reverse field whose direction is rotated 180.degree. with respect to said forward field, said forward field being along said direction of migration, said forward and reverse fields having voltage gradients and durations as follows:
- E.sub.f and E.sub.r are each greater than or equal to about 10 V/cm;
- E.sub.r /E.sub.f is greater than or equal to about 2.0;
- t.sub.f and t.sub.r are each greater than or equal to at least about 0.01 sec;
- t.sub.f /t.sub.r is greater than or equal to about 1.25;
- and E.sub.f t.sub.f /E.sub.r t.sub.r is from about 1.1 to about 2.0;
- where E.sub.f and t.sub.f are the voltage gradient and duration of said forward field and E.sub.r and t.sub.r are the voltage gradient and duration of said reverse field.
A method for the electrophoretic separation of a mixture of single strand DNA molecules of 300 or more bases in length along a preselected direction of migration in a gel, said method comprising imposing across said gel electrical fields alternating between a forward field and a reverse field whose direction is rotated 180.degree. with respect to said forward field, said forward field being along said direction of migration, said forward and reverse fields having voltage gradients and durations as follows:
- E.sub.f and E.sub.r are each from about 10 V/cm to about 100 V/cm;
- E.sub.r /E.sub.f is from about 2.0 to about 10;
- t.sub.f /t.sub.r is from about 2 to about 20;
- and
- E.sub.f t.sub.f /E.sub.r t.sub.r is from about 1.1 to about 2.0;
- where E.sub.f and t.sub.f are the voltage gradient and duration of said forward field and E.sub.r and t.sub.r are the voltage gradient and duration of said reverse field.
A method for the electrophoretic separation of a mixture of single strand DNA molecules of 300 or more bases in length along a preselected direction of migration in a gel, said method comprising imposing across said gel electrical fields alternating between a forward field and a reverse field whose direction is rotated 180.degree. with respect to said forward field, said forward field being along said direction of migration, said forward and reverse fields having voltage gradients and durations as follows:
- E.sub.f and E.sub.r are each from about 30 V/cm to about 100 V/cm;
- E.sub.r /E.sub.f is from about 2.25 to about 5;
- t.sub.f /t.sub.r is from about 2.5 to about 5;
- and
- E.sub.f t.sub.f /E.sub.r t.sub.r is from about 1.1 to about 2.0;
- where E.sub.f and t.sub.f are the voltage gradient and duration of said forward field and E.sub.r and t.sub.r are the voltage gradient and duration of said reverse field.
Dependencies are inferred from the claim text.