<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.0//EN" "http://www.ncbi.nlm.nih.gov:80/entrez/query/static/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
<PublisherName>Science and Education Publishing</PublisherName>
<JournalTitle>American Journal of Biomedical Research</JournalTitle>
<Issn>2328-3955</Issn>
<Volume>1</Volume>
<Issue>4</Issue>
<PubDate PubStatus="epublish">
<Year>2013</Year>
<Month>11</Month>
<Day>15</Day>
</PubDate>
</Journal>
<ArticleTitle>“Combinatorial Strategy”: A Highly Efficient Method for Cloning Different Vectors with Various Clone Sites</ArticleTitle>
<FirstPage>112</FirstPage>
<LastPage>119</LastPage>
<Language>EN</Language>
<AuthorList>
<Author>
<FirstName>Gang</FirstName>
<LastName>Zhang</LastName>
<Affiliation>Department of Medicine, Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Canada</Affiliation>
</Author>
<Author>
<FirstName>Anurag</FirstName>
<LastName>Tandon</LastName>
</Author>

</AuthorList>
<ArticleIdList>
<ArticleId IdType="pii">AJBR2013147</ArticleId>
<ArticleId IdType="doi">10.12691/ajbr-1-4-7</ArticleId>
</ArticleIdList>
<History>
<PubDate PubStatus="received">
<Year>2013</Year>
<Month>03</Month>
<Day>22</Day>
</PubDate>
<PubDate PubStatus="revised">
<Year>2013</Year>
<Month>10</Month>
<Day>19</Day>
</PubDate>
<PubDate PubStatus="accepted">
<Year>2013</Year>
<Month>11</Month>
<Day>15</Day>
</PubDate>
</History>
<Abstract>In this study, we generalized the “Combinatorial Strategy” for efficient cloning of different vectors with various clone sites. 1) Using originally existed clone sites from circular plasmids to prepare the inserts, if no appropriate sites available, performing SDM to create compatible sites, could achieve maximal correct digestion of the inserts. 2) Different vectors were digested with various restriction endonucleases, and then dephosphorylated after digestion. 3) Top10 competent cells were used for transformation to increase the transformant colonies. Our results showed that, when either blunt-sites or Xba I site was adopted for ligation, the percentages of positive clones were about 50%. Whereas, when different sites, including one blunt and another Pst I sites, Not I and Xho I sites, were used, the percentages of positive clones were nearly 100%. With this strategy, most vectors could be successfully cloned through “one ligation, one transformation, three to five minipreps”.</Abstract>
</Article>
</ArticleSet>
