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JPH022348A Expired / Lapsed JP ⏱️ 0.0 years remaining

Dna repair and mutation inducing method

Assignee: Abbott Laboratories
•
Filing: 1988-12-09
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Granted: —
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Expires: 2008-12-09
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Abstract

Abstract PURPOSE: To induce a site-specific mutation by simultaneously culturing a cleaved linear target DNA and an oligonucleotide having a nucleotide sequence complementary to both the side chains of the cleaved site in a proper host cell. CONSTITUTION: This method for inducing the repair and mutation of a DNA comprises cleaving the DNA at a site near to a DNA subregion to be deleted, mixing the cleaved DNA with an oligonucleotide having a nucleotide sequence complementary to both the side chains of the cleaved site and corresponding to a desired DNA sequence after the deletion, inserting the modified mixture into a cell and subsequently culturing the cell. When plasmid pWM300 is cleaved with SmaI enzyme and subsequently mutated with an oligonucleotide of the Figure, plasmid pWM301 is obtained. COPYRIGHT: (C)1990,JPO

Inventors

  • 👤 Wlodzimierz Mandecki
  • 👤 ロッツィミールツ・マンデッキ
  • 👤 Mark Allan Hayden
  • 👤 マーク・アラン・ハイデン

Bibliographic Details

Application Number —
Jurisdiction JP
Data Source google_patents
Last Synchronized 2026-11-09 18:23
CPC Classifications
C; C07; C07K; C07K14/00; C07K14/435; C07K14/46; C07K14/47; C07K14/4701; C07K14/472; C12; C12N; C12N15/00; C12N15/09; C12N15/10; C12N15/102

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