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A semi-dry, one step electroblot transfer buffer composition for rapid transfer of proteins or polypeptides from polyacrylamide gel to a suitable membrane such as nitrocellulose or polyvinylidene difluoride (PVDF). The composition contains components that minimized electrical resistance and enabled

A semi-dry, one step electroblot transfer buffer composition for rapid transfer of proteins or polypeptides from polyacrylamide gel to a suitable membrane such as nitrocellulose or polyvinylidene difluoride (PVDF). The composition contains components that minimized electrical resistance and enabled high efficiency rapid semi-dry transfer using conventional readily available filter paper, i.e., cotton cellulose fiber.

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1. An electroblot transfer method comprising: assembling a membrane and a gel, the gel containing at least one of separated proteins, peptides, or nucleic acids, the membrane and the gel sandwiched between at least two pieces of absorbent material, the absorbent material saturated with a transfer bu

1. An electroblot transfer method comprising: assembling a membrane and a gel, the gel containing at least one of separated proteins, peptides, or nucleic acids, the membrane and the gel sandwiched between at least two pieces of absorbent material, the absorbent material saturated with a transfer buffer comprising N-(2-hydroxy-1,1-bis(hydroxymethyl)ethyl)glycine (tricine), and glycine, to form a semi-dry stack; andapplying a current to effect reduced resistance in transfer of at least one of the separated proteins, polypeptides, or nucleic acids from the gel to the membrane in a semi-dry blotting procedure. 2. The method of claim 1 wherein the absorbent material is a cotton cellulose paper. 3. The method of claim 1 wherein the absorbent material is polyester cellulose. 4. The method of claim 1 wherein the transfer buffer comprises tris(hydroxymethyl)aminomethane (tris) in the range of 250 mM to 1,000 mM inclusive, glycine in the range of 250 mM to 1,000 mM inclusive, and N-(2-hydroxy-1,1-bis(hydroxymethyl)ethyl)glycine (tricine) in the range of 100 mM to 1,000 mM inclusive. 5. The method of claim 1 wherein the transfer buffer comprises tris(hydroxymethyl)aminomethane (tris) in the range of 250 mM to 350 mM inclusive, glycine in the range of 250 mM to 350 mM inclusive, and tricine in the range of 100 mM to 200 mM inclusive. 6. The method of claim 1 wherein the method transfers the at least one of separated proteins, polypeptides, or nucleic acids from the gel onto a polyvinylidene difluoride (PVDF) or nitrocellulose membrane. 7. The method of claim 1 wherein the gel is a polyacrylamide gel. 8. The method of claim 1 wherein the electroblotting of proteins and/or nucleic acids occurs in less than about 15 minutes. 9. The method of claim 1 wherein the electroblot transfer occurs using a current greater than 20 mA/cm2. 10. The method of claim 1 wherein the transfer buffer further comprises tris(hydroxymethyl)aminomethane (tris). 11. The method of claim 1 wherein the transfer buffer further comprises ethylenediaminetetraacetic acid (EDTA). 12. The method of claim 1 wherein the transfer buffer comprises ethylenediaminetetraacetic acid (EDTA) in the range of 1 mM to 100 mM inclusive. 13. The method of claim 1 wherein the absorbent material saturated with the transfer buffer provides a source of ions, and wherein said ions of said saturated absorbent material drive said transfer. 14. An electroblotting method comprising: saturating absorbent material with a transfer buffer comprising N-(2-hydroxy-1,1-bis(hydroxymethyl)ethyl)glycine (tricine) and glycine;sandwiching a membrane and a gel, the gel containing at least one of separated proteins, peptides, or nucleic acids, between at least two layers of the absorbent materialsaturated with the transfer buffer, to form a semi-dry stack; andapplying a current greater than or equal to 20 mA/cm2 in a semi-dry blotting procedure to transfer the separated proteins, peptides, and/or nucleic acids from the gel to the membrane. 15. The method of claim 14 wherein the transfer buffer further comprises tris(hydroxymethyl)aminomethane (tris). 16. The method of claim 14 wherein the transfer buffer further comprises ethylenediaminetetraacetic acid (EDTA). 17. The method of claim 14 wherein the absorbent material saturated with the transfer buffer provides a source of ions, and wherein said ions of said saturated absorbent material drive said transfer. 18. The method of claim 14 wherein the absorbent material is a cotton cellulose paper. 19. The method of claim 14 wherein the absorbent material is polyester cellulose. 20. The method of claim 14 wherein the transfer buffer comprises tris in the range of 250 mM to 1,000 mM inclusive, glycine in the range of 250 mM to 1,000 mM inclusive, and N-(2-hydroxy-1,1-bis(hydroxymethyl)ethyl)glycine (tricine) in the range of 100 mM to 1,000 mM inclusive. 21. The method of claim 14 wherein the transfer buffer comprises tris(hydroxymethyl)aminomethane (tris) in the range of 250 mM to 350 mM inclusive, glycine in the range of 250 mM to 350 mM inclusive, and tricine in the range of 100 mM to 200 mM inclusive.