Nucleic acid amplification
    11.
    发明授权
    Nucleic acid amplification 有权
    核酸扩增

    公开(公告)号:US09371557B2

    公开(公告)日:2016-06-21

    申请号:US13923232

    申请日:2013-06-20

    Abstract: In some embodiments, the present teachings provide methods for nucleic acid amplification, comprising forming a reaction mixture, and subjecting the reaction mixture to conditions suitable for nucleic acid amplification. In some embodiments, methods for nucleic acid amplification include subjecting the nucleic acid to be amplified to partially denaturing conditions. In some embodiments, methods for nucleic acid amplification include amplifying without fully denaturing the nucleic acid that is amplified. In some embodiments, the methods for nucleic acid amplification employ an enzyme that catalyzes homologous recombination and a polymerase. In some embodiments, methods for nucleic acid amplification can be conducted in a single reaction vessel. In some embodiments, methods for nucleic acid amplification can be conducted in a single continuous liquid phase of a reaction mixture, without need for compartmentalization of the reaction mixture or immobilization of reaction components. In some embodiments, methods for nucleic acid amplification comprise a amplifying at least one polynucleotide onto a surface under isothermal amplification conditions, optionally in the presence of a polymer. The polymer can include a sieving agent and/or a diffusion-reducing agent.

    Abstract translation: 在一些实施方案中,本教导提供核酸扩增方法,包括形成反应混合物,并使反应混合物经受适合于核酸扩增的条件。 在一些实施方案中,用于核酸扩增的方法包括将待扩增的核酸进行部分变性的条件。 在一些实施方案中,用于核酸扩增的方法包括扩增而不完全变性扩增的核酸。 在一些实施方案中,用于核酸扩增的方法使用催化同源重组的酶和聚合酶。 在一些实施方案中,用于核酸扩增的方法可以在单个反应容器中进行。 在一些实施方案中,用于核酸扩增的方法可以在反应混合物的单个连续液相中进行,而不需要分隔反应混合物或固定反应组分。 在一些实施方案中,用于核酸扩增的方法包括在等温扩增条件下任选地在聚合物存在下在表面上扩增至少一种多核苷酸。 聚合物可以包括筛分剂和/或扩散还原剂。

    Nucleic acid amplification
    12.
    发明授权

    公开(公告)号:US09309558B2

    公开(公告)日:2016-04-12

    申请号:US14085727

    申请日:2013-11-20

    Abstract: In some embodiments, the present teachings provide methods for nucleic acid amplification, comprising forming a reaction mixture, and subjecting the reaction mixture to conditions suitable for nucleic acid amplification. In some embodiments, methods for nucleic acid amplification include subjecting the nucleic acid to be amplified to partially denaturing conditions. In some embodiments, methods for nucleic acid amplification include amplifying without fully denaturing the nucleic acid that is amplified. In some embodiments, the methods for nucleic acid amplification employ an enzyme that catalyzes homologous recombination and a polymerase. In some embodiments, methods for nucleic acid amplification can be conducted in a single reaction vessel. In some embodiments, methods for nucleic acid amplification can be conducted in a single continuous liquid phase of a reaction mixture, without need for compartmentalization of the reaction mixture or immobilization of reaction components. In some embodiments, methods for nucleic acid amplification comprise a amplifying at least one polynucleotide onto a surface under isothermal amplification conditions, optionally in the presence of a polymer. The polymer can include a sieving agent and/or a diffusion-reducing agent.

    Nucleic acid amplification
    13.
    发明授权

    公开(公告)号:US09309557B2

    公开(公告)日:2016-04-12

    申请号:US13842296

    申请日:2013-03-15

    Abstract: In some embodiments, the present teachings provide methods for nucleic acid amplification, comprising forming a reaction mixture, and subjecting the reaction mixture to conditions suitable for nucleic acid amplification. In some embodiments, methods for nucleic acid amplification include subjecting the nucleic acid to be amplified to partially denaturing conditions. In some embodiments, methods for nucleic acid amplification include amplifying without fully denaturing the nucleic acid that is amplified. In some embodiments, the methods for nucleic acid amplification employ an enzyme that catalyzes homologous recombination and a polymerase. In some embodiments, methods for nucleic acid amplification can be conducted in a single reaction vessel. In some embodiments, methods for nucleic acid amplification can be conducted in a single continuous liquid phase of a reaction mixture, without need for compartmentalization of the reaction mixture or immobilization of reaction components. In some embodiments, methods for nucleic acid amplification comprise a amplifying at least one polynucleotide onto a surface under isothermal amplification conditions, optionally in the presence of a polymer. The polymer can include a sieving agent and/or a diffusion-reducing agent.

    Methods, compositions, systems, apparatuses and kits for nucleic acid amplification
    16.
    发明授权
    Methods, compositions, systems, apparatuses and kits for nucleic acid amplification 有权
    用于核酸扩增的方法,组合物,系统,装置和试剂盒

    公开(公告)号:US09309566B2

    公开(公告)日:2016-04-12

    申请号:US13828049

    申请日:2013-03-14

    Abstract: In some embodiments, the present teachings provide methods for paired end sequencing. In some embodiment, a polynucleotide template to be subjected to paired end sequencing comprises at least one cross linking moiety and at least one scissile moiety. In some embodiments, a paired end sequencing reaction comprises (a) a forward sequencing step, (b) a cleavage step, and (c) a reverse sequencing step. In some embodiments, a paired end sequencing reaction comprises (a) a forward sequencing step, (b) a cross-linking step, (c) a cleavage step, and (d) a reverse sequencing step.

    Abstract translation: 在一些实施方案中,本教导提供了用于配对末端测序的方法。 在一些实施方案中,待进行配对末端测序的多核苷酸模板包含至少一个交联部分和至少一个可剪切部分。 在一些实施方案中,配对末端测序反应包括(a)正向测序步骤,(b)切割步骤,和(c)反向测序步骤。 在一些实施方案中,配对末端测序反应包括(a)正向测序步骤,(b)交联步骤,(c)切割步骤和(d)反向测序步骤。

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