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        <identifier>oai:hiroshima.repo.nii.ac.jp:02006203</identifier>
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          <dc:title xml:lang="en">A heteroduplex-preferential Tm depressor for the specificity-enhanced DNA polymerase chain reactions</dc:title>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Kinoshita, Eiji</jpcoar:creatorName>
            <jpcoar:familyName xml:lang="en">Kinoshita</jpcoar:familyName>
            <jpcoar:givenName xml:lang="en">Eiji</jpcoar:givenName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Kinoshita-Kikuta, Emiko</jpcoar:creatorName>
            <jpcoar:familyName xml:lang="en">Kinoshita-Kikuta</jpcoar:familyName>
            <jpcoar:givenName xml:lang="en">Emiko</jpcoar:givenName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Koike, Tohru</jpcoar:creatorName>
            <jpcoar:familyName xml:lang="en">Koike</jpcoar:familyName>
            <jpcoar:givenName xml:lang="en">Tohru</jpcoar:givenName>
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          <dc:rights>Copyright (c) 2004 Elsevier Ltd.</dc:rights>
          <jpcoar:subject subjectScheme="Other">Macrocyclic tetraamine</jpcoar:subject>
          <jpcoar:subject subjectScheme="Other">Zinc(II) complex</jpcoar:subject>
          <jpcoar:subject subjectScheme="Other">Tm depressor</jpcoar:subject>
          <jpcoar:subject subjectScheme="Other">Specificity-enhanced PCR</jpcoar:subject>
          <jpcoar:subject subjectScheme="NDC">460</jpcoar:subject>
          <datacite:description xml:lang="en">A macrocyclic tetraamine zinc(II) complex appended with two quinoline groups, Zn2+.1,7-bis(4-quinolylmethyl)-1,4,7,10-tetraazacyclododecane (Zn2+.Q2-cyclen), was successfully used as a novel additive to suppress non-specific products in DNA polymerase chain reaction (PCR). In the presence of Zn2+.Q2-cyclen, the Tm drop of 20-bp heteroduplexes containing a non-complementary base pair was greater than that of the corresponding homoduplex (i.e., primer DNA). Here, we applied such preferential DNA melting to a specificity-enhanced PCR using micromolar concentrations of Zn2+.Q2-cyclen. We demonstrated the selective amplification of target DNA fragments (i.e., the human heart sodium channel Nav1.5 gene) from genomic DNA or a cDNA library. The optimum condition for the specificity-enhanced PCR could be determined in the concentration range of 1.50 μM of Zn2+.Q2-cyclen.</datacite:description>
          <dc:publisher>Elsevier</dc:publisher>
          <datacite:date dateType="Issued">2005-02-01</datacite:date>
          <dc:language>eng</dc:language>
          <dc:type rdf:resource="http://purl.org/coar/resource_type/c_6501">journal article</dc:type>
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            <jpcoar:relatedIdentifier identifierType="DOI">10.1016/j.ab.2004.10.009</jpcoar:relatedIdentifier>
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          <jpcoar:sourceIdentifier identifierType="ISSN">0003-2697</jpcoar:sourceIdentifier>
          <jpcoar:sourceIdentifier identifierType="NCID">AA00524867</jpcoar:sourceIdentifier>
          <jpcoar:sourceTitle>Analytical Biochemistry</jpcoar:sourceTitle>
          <jpcoar:sourceTitle>Analytical Biochemistry</jpcoar:sourceTitle>
          <jpcoar:volume>337</jpcoar:volume>
          <jpcoar:issue>1</jpcoar:issue>
          <jpcoar:pageStart>154</jpcoar:pageStart>
          <jpcoar:pageStart>154</jpcoar:pageStart>
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