1987ElectrophoresisRequires access

Transfer of proteins from plastic‐backed isoelectric focusing gels to nitrocellulose paper

George P. Albaugh, G. Ram Chandra, P.J. Bottino

Open publisher page 6 citations

Abstract

Abstract Proteins were transferred to nitrocellulose paper from plastic‐backed isoelectric focusing gels. The technique involves a two‐step blotting procedure. In the first step, simple press blotting was used to establish adhesion between the gel and overlaying nitrocellulose paper. This step facilitated the removal of the plastic backing. In the second step, electroblotting produced a pair of bi‐directional replica blots. Incubation of the gel‐nitrocellulose paper sandwich in buffers containing T ween 20 permitted the intact release of the gel from the blots. The resulting blots were successfully stained with India ink or probed with antiserum.

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What this paper is about

Abstract Proteins were transferred to nitrocellulose paper from plastic‐backed isoelectric focusing gels. The technique involves a two‐step blotting procedure. In the first step, simple press blotting was used to establish adhesion between the gel and overlaying nitrocellulose paper. This step facilitated the removal of the plastic backing. In the second step, electroblotting produced a pair of bi‐directional replica blots. Incubation of the gel‐nitrocellulose paper sandwich in buffers containing T ween 20 permitted the intact release of the gel from the blots. The resulting blots were successfully stained with India ink or probed with antiserum.

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Available abstract

Abstract Proteins were transferred to nitrocellulose paper from plastic‐backed isoelectric focusing gels. The technique involves a two‐step blotting procedure. In the first step, simple press blotting was used to establish adhesion between the gel and overlaying nitrocellulose paper. This step facilitated the removal of the plastic backing. In the second step, electroblotting produced a pair of bi‐directional replica blots. Incubation of the gel‐nitrocellulose paper sandwich in buffers containing T ween 20 permitted the intact release of the gel from the blots. The resulting blots were successfully stained with India ink or probed with antiserum.

Key concepts: Nitrocellulose, Electroblotting, Isoelectric focusing, Blot, Collodion, Chromatography, Chemistry, Antiserum

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