http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2175018-A1

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filingDate 2008-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52076188dc07a7bb9f25be7b9993cedc
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publicationDate 2010-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2175018-A1
titleOfInvention Process of clean cloning
abstract A process of inserting a nucleic acid sequence of interest into an acceptor nucleic acid, comprising the following steps: namplifying by PCR a DNA comprising in the following order a sequence segment U, a nucleic acid sequence segment of known nucleotide sequence K2 and a nucleic acid sequence segment of known sequence K3 using a forward primer defining a first end of the amplified DNA and a reverse primer defining a second end of the amplified DNA, said reverse primer terminating at its 3'-end in a nucleotide sequence of nucleic acid sequence segment K3; ntreating the linear double-stranded DNA molecules contained in the PCR product obtained in the previous step with an exonuclease to obtain a single-stranded overhang at the first end of the DNA and a single-stranded overhang comprising nucleic acid segments K2 and K3 at the second end of the DNA; nannealing the product of the previous step to a linearized double-stranded acceptor nucleic acid having at a first end thereof a single-stranded overhang complementary to the single-stranded overhang of the first end of the DNA and at a second end thereof a single-stranded overhang complementary to the single-stranded sequence segment K2 of the second end of the DNA; and ntransforming the reaction product obtained in the previous step into a host cell.
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type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 29.