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    • 27. 发明公开
    • ANALYSIS DEVICE, ANALYSIS CHIP, ANALYSIS KIT, AND ANALYSIS METHOD USING SAME
    • ANALYSEVORRICHTUNG,ANALYSECHIP,ANALYSEKIT UND ANALYSEVERFAHREN DAMIT
    • EP3144380A1
    • 2017-03-22
    • EP16743489.3
    • 2016-01-28
    • Kabushiki Kaisha Dnaform
    • TSUJIMARU Koichiro
    • C12M1/34C12M1/00C12Q1/68G01N35/08G01N37/00
    • B01L7/52B01L2300/0654B01L2300/0663B01L2300/168B01L2400/0478C12M1/00C12M1/34C12Q1/68G01N35/08G01N37/00
    • The present invention provides a tool that can analyze a target in a sample by a simple operation and can be downsized and an analysis method using the tool. By inserting an analysis chip into an analysis device, a reaction of a sample and a reagent is analyzed. The analysis chip includes a parallel flow channel in which plural reaction flow channels are connected in parallel, and the axial direction of the parallel flow channel is a direction of inserting the analysis chip into the analysis device. The analysis device includes a main body case being a housing, including an insertion opening into which the analysis chip is to be inserted; and a void; a heating unit that causes a sample to thermally react with a reagent, the heating unit being disposed in the void at at least one of inner surfaces so as to face a parallel surface of the parallel flow channel of the analysis chip; a light source unit that emits light to the analysis chip, the light source unit being disposed in the void at least above or below a reaction flow channel located at at least one end of the parallel flow channel of the analysis chip and extended along the axial direction of the parallel flow channel; and a plurality of detection units that detect the thermal reactions, each detection unit being disposed in the void at a downstream side end in the insertion direction of the analysis chip so as to correspond to each reaction flow channel of the analysis chip.
    • 本发明提供了一种能够通过简单的操作分析样本中的目标并且可以使用该工具进行小型化和分析方法的工具。 通过将分析芯片插入到分析装置中,分析样品和试剂的反应。 分析芯片包括平行流动通道,其中多个反应流动通道并联连接,并行流动通道的轴向方向是将分析芯片插入分析装置的方向。 分析装置包括:主体壳体,其是包括插入孔的壳体,分析芯片将插入其中; 和一个空白; 加热单元,其使样品与试剂发生热反应,所述加热单元设置在所述空隙中的至少一个内表面,以便面对所述分析芯片的平行流动通道的平行表面; 光源单元,其向所述分析芯片发光,所述光源单元设置在所述空隙中,所述光源单元至少位于位于所述分析芯片的平行流动通道的至少一端的反应流动通道的上方或下方,并沿着所述轴向延伸 平行流通道方向; 以及多个检测单元,其检测热反应,每个检测单元设置在分析芯片的插入方向的下游侧的空隙中,以对应于分析芯片的每个反应流动通道。
    • 28. 发明公开
    • FLUORESCENT LABELED SINGLE-STRANDED NUCLEIC ACID AND USE THEREOF
    • 维多利亚·马尔吉斯特EINZELSTRÄNGIGENUKLEINSÄUREUND VERWENDUNG DAVON
    • EP3124622A1
    • 2017-02-01
    • EP15773110.0
    • 2015-03-27
    • RikenKabushiki Kaisha DNAFORM
    • HANAMI TakeshiHAYASHIZAKI YoshihideSOMA TakahiroKIMURA Yasumasa
    • C12Q1/68C12N15/09G01N33/542
    • The present invention is intended to provide a novel fluorescent labeled single-stranded nucleic acid, by which the background of an exciton oligomer can be further reduced and the novel use thereof. The present invention relates to a labeled single-stranded nucleic acid having at least two fluorescent atomic group pairs that exhibit an exciton effect. The labeled single-stranded nucleic acid is characterized in that the emission peak wavelength of one of the fluorescent atomic group pairs (fluorescent atomic group pair A) is shorter than the excitation peak wavelength of the other fluorescent atomic group pair (fluorescent atomic group pair B), and the fluorescent atomic group pairs A and B have a Forster resonance energy transfer (FRET) effect. This fluorescent labeled single-stranded nucleic acid is usable as a primer for amplifying a target nucleic acid or a probe to be hybridized with a target nucleic acid.
    • 本发明旨在提供一种新的荧光标记单链核酸,通过其可以进一步降低激子低聚物的背景及其新用途。 本发明涉及具有表现出激子效应的至少两个荧光原子团对的标记单链核酸。 标记的单链核酸的特征在于荧光原子群对(荧光原子群对A)中的一个的发光峰值波长比另一个荧光原子群对(荧光原子群对B ),并且荧光原子群对A和B具有福斯特共振能量转移(FRET)效应。 该荧光标记的单链核酸可用作扩增靶核酸或与靶核酸杂交的探针的引物。
    • 29. 发明公开
    • Method of amplifying nucleic acid and method of detecting mutated nucleic acid using the same
    • 一种用于核酸和用于检测的方法的扩增方法的突变核酸,使得
    • EP2415878A1
    • 2012-02-08
    • EP11169071.5
    • 2004-12-24
    • RIKENKabushiki Kaisha Dnaform
    • Mitani, YasumasaOka, TakanoriHayashizaki, YoshihideHayashi, Toshizo
    • C12Q1/68
    • C12Q1/6853C12Q1/6816C12Q1/6827C12Q1/6858C12Q2537/163C12Q2531/113C12Q2521/514C12Q2525/301C12Q2525/161C12Q2537/125C12Q2522/101
    • A primer set that allows a target nucleic acid to be amplified specifically and efficiently. The primer set of the present invention includes at least two primers that allow a target nucleic acid sequence to be amplified. A first primer included in the primer set contains, in its 3' end portion, a sequence (Ac') that hybridizes to a sequence (A) located in the 3' end portion of the target nucleic acid sequence. The first primer also contains, on the 5' side of the sequence (Ac'), a sequence (B') that hybridizes to a complementary sequence (Be) to a sequence (B) that is present on the 5' side with respect to the sequence (A) in the target nucleic acid sequence. A second primer included in the primer set contains, in its 3' end portion, a sequence (Cc') that hybridizes to a sequence (C) located in the 3' end portion of a complementary sequence to the target nucleic acid sequence. The second primer also contains, on the 5' side of the sequence (Cc'), a folded sequence (D-Dc') that contains, on the same strand, two nucleic acid sequences that hybridize to each other.
    • 一种引物组确实允许靶核酸可以特异且高效地扩增。 所述引物组,本发明的包括至少两个引物确实允许目标核酸序列进行扩增。 包括在所述引物组的第一引物包含在其3“端部分,一序列(AC”)没有杂交到位于靶核酸序列的3“端部分序列(A)。 因此,第一引物含有,对“(,序列(B”)的5序列AC)的侧“做杂交的互补序列(BE)的序列(B)那样存在于5”侧相对于 在靶核酸序列的序列(A)。 包括在所述引物组的第二引物含有,在其3“端部分,一序列(CC”)没有杂交到位于互补序列与靶核酸序列的3“端部分的序列(C)。 因此,第二引物含有,对“(5序列CC)的侧”,折叠序列(D-DC“)确实包含,在相同的海滩,两个核酸序列杂交并海誓山盟。