<?xml version="1.0"?>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mi#PSI-MI_slim"/>
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    <!-- 
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    <!-- http://purl.obolibrary.org/obo/MI_0009 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MI_0009">
        <rdfs:label>bacterial display</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MI_0034"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MI_0054"/>
        <oboInOwl:id>MI:0009</oboInOwl:id>
        <ns3:IAO_0000115>The protein of interest is presented on the outer membrane of Gram negative bacteria by expressing it as a fusion partner to peptide signals that direct heterologous proteins to the cell surface. For instance, a single chain Fv (scFv) antibody fragment, consisting of the variable heavy and variable light domains from two separate anti-digoxin monoclonal antibodies, was displayed on the outer membrane of Escherichia coli by fusing it to an Lpp-OmpA. Similar systems have also been developed for gram positive bacteria. Fluorescence-activated cell sorting (FACS), is used to specifically select clones displaying a protein binding to scFv-producing cells.</ns3:IAO_0000115>
        <oboInOwl:hasOBONamespace>PSI-MI</oboInOwl:hasOBONamespace>
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    <!-- http://purl.obolibrary.org/obo/MI_0034 -->

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        <rdfs:label>display technology</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MI_0054 -->

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        <rdfs:label>fluorescence-activated cell sorting</rdfs:label>
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