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  <eprint id='http://eprints.iliauni.edu.ge/id/eprint/485'>
    <eprintid>485</eprintid>
    <rev_number>7</rev_number>
    <eprint_status>archive</eprint_status>
    <userid>90</userid>
    <dir>disk0/00/00/04/85</dir>
    <datestamp>2014-01-23 19:22:47</datestamp>
    <lastmod>2014-01-23 19:22:47</lastmod>
    <status_changed>2014-01-23 19:22:47</status_changed>
    <type>article</type>
    <metadata_visibility>no_search</metadata_visibility>
    <contact_email>neli_datukishvili@iliauni.edu.ge</contact_email>
    <creators>
      <item>
        <name>
          <family>Kutateladze</family>
          <given>Tamara / T. </given>
        </name>
      </item>
      <item>
        <name>
          <family>Gabriadze</family>
          <given>Inga / I. </given>
        </name>
      </item>
      <item>
        <name>
          <family>Datukishvili</family>
          <given>Nelly / N. </given>
        </name>
        <id>neli_datukishvili@iliauni.edu.ge</id>
      </item>
      <item>
        <name>
          <family>Karseladze</family>
          <given>Marina / M. </given>
        </name>
      </item>
      <item>
        <name>
          <family>Zaalishvili </family>
          <given>Tengiz / T. </given>
        </name>
      </item>
    </creators>
    <title>Screening of genetically modified plants by duplex PCR </title>
    <ispublished>pub</ispublished>
    <subjects>
      <item>SB</item>
    </subjects>
    <divisions>
      <item>fac_med</item>
    </divisions>
    <full_text_status>none</full_text_status>
    <abstract>Two duplex polymerase chain reactions were developed for screening genetically modified plants. The certified reference materials as dried powders containing 0-5% Roundup Ready soybean and maize MON-810 were used for optimization and validation of PCR methods. The genomic DNAs were extracted by Qiagen DNeasy plant mini kit and analysed using species-specific and GMO-specific uniplex PCR. The PCR products were evaluated by agarose gel electrophoresis. Different combinations of the GMO-specific primers were verified for their suitability for duplex PCR. Two duplex PCRs were developed and optimized, that allow simultaneous detection of two common transgenic elements, such as: cauliflower mosaic virus (CaMV) 35S promoter and Agrobacterium tumefaciens nopaline synthase (NOS) terminator. The developed duplex PCRs are effective tools for rapid and cheap screening of transgenic plants. </abstract>
    <date>2013-01</date>
    <date_type>published</date_type>
    <publication>Annals of Agrarian Science</publication>
    <volume>11</volume>
    <number>1</number>
    <pagerange>76-79</pagerange>
    <refereed>TRUE</refereed>
    <issn>1512-1887</issn>
    <official_url>http://www.agrscience.ge/content/content11_1.pdf</official_url>
    <related_url>
      <item>
        <url>http://www.agrscience.ge/Agrarian%20Science-main.htm</url>
        <type>pub</type>
      </item>
    </related_url>
    <projects>
      <item>Shota Rustaveli National science Foundation Grant # GRANT/ST 09_262_8-150</item>
    </projects>
  </eprint>
</eprints>
