发明名称 |
DEVICE AND METHOD FOR QUANTIFYING GENE |
摘要 |
PROBLEM TO BE SOLVED: To enable the gene amplification by a PCR method to be simply carried out, and to enable the determination to be carried out over a wide range like a real-time PCR, and highly reliable quantitative data to be obtained. SOLUTION: PCR cycles are repeated by flowing a sample liquid in a PCR plate 3 having a denaturation temperature region A1 and an annealing temperature region A2 parallelly formed along the longitudinal direction X, and a capillary passage 2 progressing in the longitudinal direction while moving between the temperature regions A1 and A2 at both sides so as to meander, and the fluorescent intensity in each capillary passage 2 is measured so as to correspond to the number of the PCR cycles by moving an optical head 5 for measuring the fluorescent intensity. COPYRIGHT: (C)2008,JPO&INPIT
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申请公布号 |
JP2007300896(A) |
申请公布日期 |
2007.11.22 |
申请号 |
JP20060135516 |
申请日期 |
2006.05.15 |
申请人 |
ISHIKAWA PREF GOV;JAPAN ADVANCED INSTITUTE OF SCIENCE & TECHNOLOGY HOKURIKU;MORITEX CORP |
发明人 |
NAKANO KOICHI;YONEZAWA YUJI;TAMIYA EIICHI;NAKAYAMA TAKESHI;MIYOUGADANI TORU;YUMINO TAKESHI |
分类号 |
C12M1/00;C12N15/09;C12Q1/68 |
主分类号 |
C12M1/00 |
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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