Summary
Multiple antigenic peptides (MAPs) can be efficiently separated on sodium dodecyl sulfate (SDS) polyacrylamide gel and transferred to a nitrocellulose membrane for immunoblotting. MAPs involve a hepta lysine core with end groups for anchoring multiple copies of the same synthetic peptide. MAPs are amenable to staining with Coomassie and silver on SDS polyacrylamide gels as well as by Fast Green on a blotted nitrocellulose membrane. They lend themselves to analysis on an immunoblot as they behave like low molecular weight proteins. Affinity immunoblotting for analysis of antibody clonotype distribution has also been carried out using these peptides.
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Acknowledgement
This work was supported by NIH grant ARO1844 and Oklahoma Center for the Advancement of Science and Technology to Dr. Hal Scofield, OMRF, OKC, OK, USA.
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Kurien, B.T. (2009). Strip Immunoblotting of Multiple Antigenic Peptides to Nitrocellulose Membrane. In: Kurien, B., Scofield, R. (eds) Protein Blotting and Detection. Methods in Molecular Biology, vol 536. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59745-542-8_21
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DOI: https://doi.org/10.1007/978-1-59745-542-8_21
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