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公开(公告)号:US10975415B2
公开(公告)日:2021-04-13
申请号:US15507796
申请日:2015-09-09
申请人: TAKARA BIO INC. , KYUSHU UNIVERSITY, NATIONAL UNIVERSITY CORPORATION , EDUCATIONAL CORPORATION KANSAI BUNRI SOUGOUGAKUEN
发明人: Takashi Uemori , Yoshizumi Ishino , Takehiro Sagara , Sonoko Ishino , Takeshi Yamagami , Tsuyoshi Shirai
摘要: A polypeptide having a mismatch endonuclease activity of recognizing a mismatch and cleaving the mismatch; a mismatch-specific cleavage reaction using the polypeptide; a method for removing an error in a nucleic acid amplification reaction utilizing the polypeptide; a method for inhibiting the amplification of a nucleic acid comprising a specific nucleotide sequence during a nucleic acid amplification reaction; and a method for detecting a nucleic acid having a single-nucleotide polymorphism mutation utilizing the inhibition method.
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公开(公告)号:US11046939B2
公开(公告)日:2021-06-29
申请号:US15779247
申请日:2016-11-24
摘要: The present invention relates to a Thermus aquaticus (Taq) polymerase having a strand displacement activity in which an amino acid residue in a template DNA binding site of the DNA polymerase is substituted with an amino acid to increase a total charge in the site, a nucleic acid encoding the polymerase, a vector containing the nucleic acid, a transformant containing the vector containing the nucleic acid or the nucleic acid, a method for producing the polymerase, a method for amplifying nucleic acids utilizing the polymerase, and a kit containing the polymerase. According to the present invention, a DNA polymerase having a high thermostability, capable of efficiently replicating a long-strand of a template DNA, and having a strong strand displacement activity is provided.
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公开(公告)号:US10533162B2
公开(公告)日:2020-01-14
申请号:US15855882
申请日:2017-12-27
摘要: Provided are various novel DNA polymerases.Provided are: a DNA polymerase comprising: an amino acid sequence modified from the amino acid sequence of SEQ ID NO: 12, which has a substitution of arginine at position 651 by an amino acid residue having a negatively charged side chain, preferably by asparatic acid or glutamic acid, more preferably by glutamic acid; and a DNA polymerase comprising an amino acid sequence modified from the amino acid sequence of SEQ ID NO: 14, which has a substitution of proline at position 653 by an amino acid residue having a negatively charged side chain, preferably by asparatic acid or glutamic acid, more preferably by glutamic acid.
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公开(公告)号:US09840700B2
公开(公告)日:2017-12-12
申请号:US14890009
申请日:2014-05-09
CPC分类号: C12N9/22 , C12N15/102 , C12Y301/00
摘要: There is provided an enzyme which has an activity of cleaving a phosphodiester bond of deoxyribonucleotide having a damaged base and deoxyribonucleotide adjacent to the 5′ side of the deoxyribonucleotide in DNA strands which contain the damaged base as a reagent or the like for manipulating a gene, and further provided a method of removing a damaged base from DNA strands using the enzyme.
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