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    • 4. 发明申请
    • METHOD FOR AMPLIFYING DNA FRAGMENT
    • 放大DNA片段的方法
    • US20100120036A1
    • 2010-05-13
    • US12530033
    • 2008-03-05
    • Kunio ShiotaShintaro YagiYoko TakahashiSatoshi TanakaJun Ohgane
    • Kunio ShiotaShintaro YagiYoko TakahashiSatoshi TanakaJun Ohgane
    • C12Q1/68C12P19/34
    • C12Q1/683C12Q2531/113C12Q2525/155C12Q2521/331
    • To measure the methylation degree of a genomic DNA simply and correctly as well as exhaustively, there is provided a method for amplifying a DNA fragment, characterized by comprising the following steps (1) to (5): (1) digesting a sample double-stranded DNA with a first restriction enzyme; (2) adding a double-stranded DNA fragment consisting of a first oligonucleotide and a second oligonucleotide to a restriction enzyme cleavage end of the double-stranded DNA fragment produced in step (1) to obtain a DNA fragment; (3) digesting the DNA fragment obtained in step (2) with a second restriction enzyme; (4) allowing the double-stranded DNA fragment produced in step (3) to coexist with a third oligonucleotide and a fourth oligonucleotide in the presence of a ligase; and (5) heating the double-stranded DNA fragment obtained in step (4), thereby dissociating the double-stranded DNA fragment and then performing a polymerase chain reaction to selectively amplify a DNA fragment having the cleavage end of the first restriction enzyme and the cleavage end of the second restriction enzyme.
    • 为了简单正确地,全面地测定基因组DNA的甲基化程度,提供了扩增DNA片段的方法,其特征在于包括以下步骤(1)〜(5):(1) 用第一限制酶的双链DNA; (2)将由第一寡核苷酸和第二寡核苷酸组成的双链DNA片段加入步骤(1)中制备的双链DNA片段的限制酶切割末端以获得DNA片段; (3)用第二限制酶消化步骤(2)中获得的DNA片段; (4)在连接酶存在下使步骤(3)中产生的双链DNA片段与第三寡核苷酸和第四寡核苷酸共存; (5)加热步骤(4)中获得的双链DNA片段,从而解离双链DNA片段,然后进行聚合酶链式反应以选择性扩增具有第一限制酶切割末端的DNA片段, 第二限制酶的切割末端。
    • 5. 发明授权
    • Methods for the detection of hepatitis B and C viruses
    • 检测乙型和丙型肝炎病毒的方法
    • US07776542B1
    • 2010-08-17
    • US09269897
    • 1998-08-04
    • Katsumi AoyagiChiharu OhueKumiko IidaTatsuji KimuraShintaro Yagi
    • Katsumi AoyagiChiharu OhueKumiko IidaTatsuji KimuraShintaro Yagi
    • G01N33/53G01N33/569G01N33/576
    • G01N33/5767G01N33/56983G01N2333/02G01N2333/18
    • A method for treating a virus-containing sample, characterized by treatment of a virus-containing sample with a treatment solution containing (1) an anionic surfactant and (2) an amphoteric surfactant, nonionic surfactant or protein denaturant; a virus assay method using said treating method; a method for treating a virus-containing sample, characterized by treatment of a virus-containing sample with a treatment solution containing (1) a chaotropic ion and (2) an acidifying agent; a virus assay method using said treating method; a virus assay method, characterized in that a virus antigen and a virus antibody are measured based on their binding to their probe in the presence of a surfactant with an alkyl group of 10 or more carbon atoms and a secondary, tertiary or quaternary amine, or a nonionic surfactant, or of both of them; and a monoclonal antibody and a hybridoma producing the same for carrying out said method.
    • 一种治疗含病毒样品的方法,其特征在于用含有(1)阴离子表面活性剂和(2)两性表面活性剂,非离子表面活性剂或蛋白质变性剂的处理溶液处理病毒样品; 使用所述处理方法的病毒测定方法; 一种用于处理含病毒样品的方法,其特征在于用含有(1)离液序列离子的处理溶液和(2)酸化剂处理含有病毒的样品; 使用所述处理方法的病毒测定方法; 一种病毒测定方法,其特征在于,在具有10个或更多个碳原子的烷基和二级,三级或季胺的表面活性剂存在下,基于它们与它们的探针的结合来测量病毒抗原和病毒抗体,或 非离子表面活性剂,或它们两者; 以及用于实施所述方法的单克隆抗体和产生其的杂交瘤。