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    <!-- http://purl.obolibrary.org/obo/ECO_0000009 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/ECO_0000009">
        <rdfs:label>transcript expression evidence</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/ECO_0001819 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/ECO_0001819">
        <rdfs:label>primer extension assay evidence</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/ECO_0000009"/>
        <oboInOwl:created_by>swolfish</oboInOwl:created_by>
        <oboInOwl:hasOBONamespace>eco</oboInOwl:hasOBONamespace>
        <ns2:IAO_0000112>The primer extension assay (Fig. 6a) defined the transcription start sites the three sRNA genes qrr2 - 4, and this assay also indicated that the promoter activity of all the thee qrr genes was under the positive control of OpaR.</ns2:IAO_0000112>
        <rdfs:comment>The most commonly used radiolabel is 32P.</rdfs:comment>
        <ns2:IAO_0000234>CollecTF</ns2:IAO_0000234>
        <ns2:IAO_0000115>A type of transcript expression evidence used to determine expression levels of mRNA where a labeled synthetic oligonucleotide primer is annealed to mRNA downstream of the presumed transcription start site of a gene. The mRNA is extended with reverse transcriptase, producing cDNA which is electrophoresed, and the band size is enables determination of the 5&#39; end of the mRNA (i.e. the transcription start site).</ns2:IAO_0000115>
        <ns2:IAO_0000112>The primer extension assay detected two transcriptional start sites located at 343 and 78 bp upstream of rovA (Fig. 2); therefore, two promoters (named P2 and P1, respectively) were transcribed for rovA.</ns2:IAO_0000112>
        <oboInOwl:id>ECO:0001819</oboInOwl:id>
        <oboInOwl:creation_date>2015-11-04T09:33:18Z</oboInOwl:creation_date>
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