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    <dc:description xml:lang="en">&lt;div&gt;&lt;img src="/dbfiles/SciNetS_ria61i/PSC_Logo1.png" width="65" height="69"&gt;&lt;img src="/dbfiles/SciNetS_ria61i/P_NECSoft_horizontal.png" width="240" height="46"&gt;&lt;/div&gt;&lt;div style="clear: both; -moz-border-radius: 10px 10px 10px 10px; padding: 10px; border: 3px double rgb(178, 178, 128); width: 800px; background: none repeat scroll 0% 0% rgb(255, 255, 238);"&gt;　We collected each full-length cDNAs prepared in RIKEN into an almost equimolarratio to generate plant expression library. In this library each full-lengthcDNA is located under CaMV35S promoter and TMV omega sequence for properprotein production. As a starting material we have collected around 10,000independent full-length cDNAs. By Agrobacteria inplanta transformation methoddeveloped in Arabidopsis we could transfer T-DNA region of the plant expressionlibrary into &lt;em&gt;Arabidopsis&lt;/em&gt;. By repeating this transformation procedure we havegenerated around 30,000 independent &lt;em&gt;Arabidopsis&lt;/em&gt; transgenic lines overexpressingfull-length cDNAs (FOX &lt;em&gt;Arabidopsis&lt;/em&gt; mutant lines). For detail method of thelibrary construction, please refer to &lt;a href="http://www3.interscience.wiley.com/journal/118565276/abstract?CRETRY=1&amp;amp;SRETRY=0"&gt;Ichikawa et al., The Plant Journal (2006)45, 974-985&lt;/a&gt;. All contents in this database have been constructed bycollaboration with &lt;a href="http://www.necsoft.com"&gt;NEC Soft, Ltd&lt;/a&gt; (VALWAY Technology Center, NEC Soft, Ltd,Tokyo, Japan).&lt;/div&gt;</dc:description>
    <dc:description xml:lang="ja">&lt;div&gt;&lt;img src="/dbfiles/SciNetS_ria61i/PSC_Logo1.png" width="65" height="69"&gt;&lt;img src="/dbfiles/SciNetS_ria61i/P_NECSoft_horizontal.png" width="240" height="46"&gt;&lt;/div&gt;&lt;div style="clear: both; -moz-border-radius: 10px 10px 10px 10px; padding: 10px; border: 3px double rgb(178, 178, 128); width: 800px; background: none repeat scroll 0% 0% rgb(255, 255, 238);"&gt;　We collected each full-length cDNAs prepared in RIKEN into an almost equimolarratio to generate plant expression library. In this library each full-lengthcDNA is located under CaMV35S promoter and TMV omega sequence for properprotein production. As a starting material we have collected around 10,000independent full-length cDNAs. By Agrobacteria inplanta transformation methoddeveloped in Arabidopsis we could transfer T-DNA region of the plant expressionlibrary into &lt;em&gt;Arabidopsis&lt;/em&gt;. By repeating this transformation procedure we havegenerated around 30,000 independent &lt;em&gt;Arabidopsis&lt;/em&gt; transgenic lines overexpressingfull-length cDNAs (FOX &lt;em&gt;Arabidopsis&lt;/em&gt; mutant lines). For detail method of thelibrary construction, please refer to &lt;a href="http://www3.interscience.wiley.com/journal/118565276/abstract?CRETRY=1&amp;amp;SRETRY=0"&gt;Ichikawa et al., The Plant Journal (2006)45, 974-985&lt;/a&gt;. All contents in this database have been constructed bycollaboration with &lt;a href="http://www.necsoft.com"&gt;NEC Soft, Ltd&lt;/a&gt; (VALWAY Technology Center, NEC Soft, Ltd,Tokyo, Japan).&lt;/div&gt;</dc:description>
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    <rdfs:label xml:lang="en">FOX Hunting </rdfs:label>
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    <dcterms:description xml:lang="ja">Imported from SciNetS</dcterms:description>
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