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dc.contributor.authorGrallert, Agnes
dc.contributor.authorHagan, Iain M
dc.date.accessioned2017-03-04T20:25:42Z
dc.date.available2017-03-04T20:25:42Z
dc.date.issued2017-02-01
dc.identifier.citationSmall-scale immunoprecipitation from fission yeast cell extracts. 2017, Cold Spring Harb Protocen
dc.identifier.issn1559-6095
dc.identifier.pmid28148852
dc.identifier.doi10.1101/pdb.prot091587
dc.identifier.urihttp://hdl.handle.net/10541/620186
dc.description.abstractWe describe procedures for the immunoprecipitation (IP) of a molecule of interest from cell extracts under native or denaturing conditions. The methods are equally effective with antibodies that directly recognize the molecule of interest and those that recognize a generic peptide "epitope tag" that has been fused to sequences encoding the gene of interest. The diverse chemistry of intermolecular interactions and enzymatic activities means that a range of different buffer conditions must be assessed empirically to identify optimal conditions for the study of a specific target/complex in a particular assay. We describe three buffers that can serve as starting points for this empirical testing and discuss modifications that are commonly used in the optimization of assays based on immunoprecipitation.
dc.language.isoenen
dc.rightsArchived with thanks to Cold Spring Harbor protocolsen
dc.titleSmall-scale immunoprecipitation from fission yeast cell extracts.en
dc.typeArticleen
dc.contributor.departmentCRUK Cell Division Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester M20 4BX, United Kingdomen
dc.identifier.journalCold Spring Harbor Protocolsen
html.description.abstractWe describe procedures for the immunoprecipitation (IP) of a molecule of interest from cell extracts under native or denaturing conditions. The methods are equally effective with antibodies that directly recognize the molecule of interest and those that recognize a generic peptide "epitope tag" that has been fused to sequences encoding the gene of interest. The diverse chemistry of intermolecular interactions and enzymatic activities means that a range of different buffer conditions must be assessed empirically to identify optimal conditions for the study of a specific target/complex in a particular assay. We describe three buffers that can serve as starting points for this empirical testing and discuss modifications that are commonly used in the optimization of assays based on immunoprecipitation.


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