System for rapid high-resolution gel electrophoresis
Abstract
Electrophoretic systems, formulations and methods are described which allow a user to perform electrophoresis experiments under conditions of high voltage and with reduced run time. An electrophoretic system, formulation or method may be run at 50% higher field strength than comparable systems already in use in the art. The presently described systems and formulations may be run at voltages above 225 V, above 250 V, above 275 V, above 300 V, above 325 V or above 350 V. The time required for performing an electrophoresis experiment may be reduced to less than about 30 minutes, less than about 20 minutes, less than about 15 minutes or less than about 12 minutes.
Claims
exact text as granted — not AI-modified1 . A discontinuous buffer electrophoretic system comprising:
an electrophoretic separation gel, said electrophoretic separation gel comprising a gel buffer system, said buffer system comprising: a gel amine buffer; and a gel ampholyte; and an aqueous running buffer comprising a buffer ampholyte.
2 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the separation gel comprises acrylamide, agarose, or acrylamide and agarose.
3 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the separation gel comprises acrylamide.
4 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the separation gel comprises between about 6 to about 25 wt. % acrylamide.
5 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the separation gel comprises between about 8 to about 20 wt. % acrylamide.
6 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the separation gel comprises between about 8 to about 15 wt. % acrylamide.
7 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the electrophoretic separation gel further comprises a stacking gel coupled to one end thereof.
8 . The discontinuous buffer electrophoretic system according to claim 7 , wherein the stacking gel comprises about 4 wt. % acrylamide.
9 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the gel ampholyte is different from the buffer ampholyte.
10 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the pK of the gel amine buffer is in the range of about 5.5 to about 7.5.
11 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the gel amine buffer is Bis-Tris.
12 . The discontinuous buffer electrophoretic system according to either claim 10 or claim 11 , wherein the concentration of the gel amine buffer is in the range of about 190 mM to about 295 mM.
13 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the concentration of the gel amine buffer is less than about 300 mM.
14 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the concentration of the gel amine buffer is between about 175 mM to about 300 mM.
15 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the pK of the gel ampholyte is about 1.5 pK units greater than the pK of the gel amine.
16 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the pK of the gel ampholyte is between about 7 to about 9.
17 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the pK of the gel ampholyte is between about 8 to about 8.5.
18 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the pK of the gel ampholyte is between about 8.1 to about 8.3.
19 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the gel ampholyte is Tricine, Bicine, glycinamide or acetamidoglycine.
20 . The discontinuous buffer electrophoretic system according to claim 1 , wherein the gel ampholyte is Tricine or Bicine.
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