METHOD, MICROREACTOR AND APPARATUS FOR CARRYING OUT REAL-TIME NUCLEIC ACID AMPLIFICATION
    2.
    发明申请
    METHOD, MICROREACTOR AND APPARATUS FOR CARRYING OUT REAL-TIME NUCLEIC ACID AMPLIFICATION 审中-公开
    用于实时实时核酸放大的方法,微生物和装置

    公开(公告)号:WO2010076189A1

    公开(公告)日:2010-07-08

    申请号:PCT/EP2009/067167

    申请日:2009-12-15

    Abstract: A method for carrying out nucleic acid amplification, includes providing a reaction chamber (31), accommodating an array (36) of nucleic acid probes (37) at respective locations, for hybridizing to respective target nucleic acids; and introducing a solution (50) into the reaction chamber (31), wherein the solution (50) contains primers, capable of binding to target nucleic acids, nucleotides, nucleic acid extending enzymes and a sample including nucleic acids. The a structure of the nucleic acid probes (37) and of the primers so that a hybridization temperature (T H ) of the probes (37) is higher than an annealing temperature (T A ) of the primers, whereby hybridization and annealing take place in respective separate temperature ranges (R H , R A ).

    Abstract translation: 一种用于进行核酸扩增的方法,包括提供在相应位置容纳核酸探针(37)的阵列(36)的反应室(31),用于与各自的靶核酸杂交; 以及将溶液(50)引入所述反应室(31)中,其中所述溶液(50)含有能够结合靶核酸,核苷酸,核酸延伸酶和包含核酸的样品的引物。 核酸探针(37)的结构和引物的结构使得探针(37)的杂交温度(TH)高于引物的退火温度(TA),由此在各自的条件下进行杂交和退火 分开的温度范围(RH,RA)。

    METHOD, MICROREACTOR AND APPARATUS FOR CARRYING OUT REAL-TIME NUCLEIC ACID AMPLIFICATION
    3.
    发明公开
    METHOD, MICROREACTOR AND APPARATUS FOR CARRYING OUT REAL-TIME NUCLEIC ACID AMPLIFICATION 审中-公开
    法,微反应器和设备,用于实时进行核酸扩增

    公开(公告)号:EP2382324A1

    公开(公告)日:2011-11-02

    申请号:EP09799323.2

    申请日:2009-12-15

    Abstract: A method for carrying out nucleic acid amplification, includes providing a reaction chamber (31), accommodating an array (36) of nucleic acid probes (37) at respective locations; for hybridizing to respective target nucleic acids; and introducing a solution (50) into the reaction chamber (31), wherein the solution (50) contains primers, capable of binding to target nucleic acids, nucleotides, nucleic acid extending enzymes and a sample including nucleic acids. The structure of the nucleic acid probes (37) and of the primers is selected so that a hybridization temperature (TH) of the probes (37) is higher than an annealing temperature (TA) of the primers, whereby hybridization and annealing take place in respective separate (non-overlapping) temperature ranges (RH, RA).

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