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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/MI_0413 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MI_0413">
        <rdfs:label>electrophoretic mobility shift assay</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MI_0807"/>
        <oboInOwl:hasOBONamespace>PSI-MI</oboInOwl:hasOBONamespace>
        <oboInOwl:id>MI:0413</oboInOwl:id>
        <oboInOwl:hasExactSynonym>band shift</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>This method proves the interaction between a nucleic acid and a protein partner. On the same electrophoresis gel 1 lane is loaded with a nucleic acid of known sequence, a second lane is loaded with the same nucleic acid together with a purified protein (or a protein mixture). The nucleic acid is often radio-labelled to enable visualisation by autoradiography. Comparison of the nucleic acid migration in the two lanes enables the retardation of the nucleic acid due to its interaction with a protein to be observed.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>emsa</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Gel retardation assay</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MI_0807 -->

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