Crossed immunoelectrophoresis from sodium dodecyl sulfate-polyacrylamide gels into antibody-containing agarose: An improved method for evaluation of the number of immunochemical determinants in polypeptides, with reference to spectrin
Autor: | F. H. Kirkpatrick, Donald J. Rose |
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Rok vydání: | 1978 |
Předmět: |
Polyacrylamide
Biophysics Peptide Fluorescamine Biochemistry Antibodies Epitopes chemistry.chemical_compound Humans Spectrin Sodium dodecyl sulfate Immunoelectrophoresis Molecular Biology chemistry.chemical_classification Chromatography Staining and Labeling Chemistry Sepharose Erythrocyte Membrane Membrane Proteins Sodium Dodecyl Sulfate Cell Biology Precipitin Electrophoresis Agarose Immunoelectrophoresis Two-Dimensional |
Zdroj: | Analytical Biochemistry. 89:130-135 |
ISSN: | 0003-2697 |
DOI: | 10.1016/0003-2697(78)90733-9 |
Popis: | A simple method is described for performing crossed immunoelectrophoresis into antibody-containing agarose when the first-dimension gel contains peptides separated by electrophoresis in sodium dodecyl sulfate. Artifacts produced by sodium dodecyl sulfate are avoided by incorporation of Triton X-100 in the agarose layer. Peptides are located by prestaining (before SDS-acrylamide electrophoresis) with the cycloheptylamylose complex of fluorescamine. Injection of ink into prestained peptide bands produces a line extending from the peptide band location to its precipitin arc, thereby allowing unambiguous assignment of arcs to peptides in situations where peptide bands are not widely separated. The utility of this procedure is illustrated for the erythrocyte membrane protein spectrin. |
Databáze: | OpenAIRE |
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