发明名称 |
Method for synthesizing DNA |
摘要 |
A DNA synthesis method with a shortened time period required for DNA synthesis by polymerase chain reaction (PCR), characterized in that a DNA polymerase is used in an amount effective for providing more than 10 ng of amplified DNA fragments of about 2 kb per 50 µl of a reaction mixture, when PCR is carried out under the following conditions (A) and (B): (A) reaction mixture: 50 µl volume of a reaction mixture comprising DNA polymerase, 1 ng of genomic DNA from Escherichia coli , and 10 pmol each of primers Eco-1 and Eco-2 (nucleotide sequences of the primers Eco-1 and Eco-2 being shown in SEQ ID NOs: 10 and 11 of Sequence Listing, respectively); and having a composition suitable for the DNA polymerase; and (B) reaction conditions: 35 cycles of PCR, wherein one cycle consists of 99°C, 1 second - 66°C, 7 seconds; a kit for DNA synthesis usable for the DNA synthesis method; and an article of manufacture of a PCR agent. According to the present invention, the procedures in the genetic engineering studies and industries involved with PCR can be speeded up.
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申请公布号 |
EP1607480(A2) |
申请公布日期 |
2005.12.21 |
申请号 |
EP20050005778 |
申请日期 |
1999.09.06 |
申请人 |
TAKARA BIO INC. |
发明人 |
UEMORI, TAKASHI;SATO, YOSHIMI;OKAWA, MARIKO;FUJITA, TOMOKO;MIYAKE, KAZUE;TAKEDA, OSAMU;SAGAWA, HIROAKI;HAGIYA, MICHIO;MUKAI, HIROYUKI;ASADA, KIYOZO;KATO, IKUNOSHIN |
分类号 |
C12N15/11;C12N15/10;C12P19/34;C12Q1/68;G01N33/53;(IPC1-7):C12N15/11 |
主分类号 |
C12N15/11 |
代理机构 |
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代理人 |
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主权项 |
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地址 |
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