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    • 58. 发明授权
    • Polymerase incorporation of non-standard nucleotides
    • 聚合酶掺入非标准核苷酸
    • US08614072B2
    • 2013-12-24
    • US12999138
    • 2009-06-16
    • Steven Albert BennerZunyi Yang
    • Steven Albert BennerZunyi Yang
    • C12P19/34C12Q1/68
    • C12Q1/6853C12P19/34C12Q1/686C12Q2521/101C12Q2525/117C12Q2525/191
    • The disclosed invention teaches processes to amplify oligonucleotides by contacting templates and primers with DNA polymerases and triphosphates of non-standard nucleotides, which form nucleobase pairs fitting the standard Watson-Crick geometry, but joined by hydrogen bonding patterns different from those that join standard A:T and G:C pairs. Thus, this invention relates to nucleotide analogs and their derivatives that, when incorporated into DNA and RNA, expand the number of replicatable nucleotides beyond the four found in standard DNA and RNA. The invention further relates to polymerases that incorporate those non-standard nucleotide analogs into oligonucleotide products using the corresponding triphosphate derivatives, and more specifically, polymerases and non-standard nucleoside triphosphates that support the polymerase chain reaction (PCR), including PCR where the products contain more than one non-standard nucleotide unit.
    • 所公开的发明教导了通过使模板和引物与DNA聚合酶和非标准核苷酸的三磷酸接触来扩增寡核苷酸的过程,其形成适合标准Watson-Crick几何形状的核碱基对,但是通过与加入标准A: T和G:C对。 因此,本发明涉及核苷酸类似物及其衍生物,其在掺入DNA和RNA时扩大超出标准DNA和RNA中发现的四种可重复核苷酸的数量。 本发明还涉及使用相应的三磷酸衍生物,更具体地,支持聚合酶链式反应(PCR)的聚合酶和非标准核苷三磷酸(包括产物含有的PCR)的寡核苷酸产物,将这些非标准核苷酸类似物结合到聚合酶中的聚合酶 多个非标准核苷酸单位。
    • 60. 发明申请
    • Nanopore Based Molecular Detection and Sequencing
    • 基于纳米孔的分子检测和测序
    • US20130244340A1
    • 2013-09-19
    • US13745688
    • 2013-01-18
    • GENIA TECHNOLOGIES, INC.
    • Randall DavisRoger Chen
    • C12Q1/68
    • C12Q1/6869C12Q1/6874G01N33/48721C12Q2521/101C12Q2565/607
    • This disclosure provides systems and methods for molecular identification and polymer (e.g., nucleic acid) sequencing using nanopores. The polymer may be passed through or in proximity to the nanopore and various subunits of the polymer may affect the current flowing through the nanopore. The various subunits may be identified by measuring the current at a plurality of voltages applied across the nanopore and/or membrane. In some cases, the polymerization of tagged nucleotides presents tag molecules to the nanopore that can be identified by measuring the current at a plurality of voltages applied across the nanopore and/or membrane. Also provided herein are systems and methods for sequencing both the sense and anti-sense strand of a double stranded nucleic acid molecule with a nanopore and methods for using ribonucleic acid (RNA) speed bump molecules to slow the passage of a nucleic acid molecule through or in proximity to a nanopore.
    • 本公开提供用于分子鉴定和使用纳米孔的聚合物(例如,核酸)测序的系统和方法。 聚合物可以通过纳米孔或靠近纳米孔,聚合物的各种亚基可能影响流过纳米孔的电流。 可以通过测量跨过纳米孔和/或膜施加的多个电压的电流来识别各种亚基。 在一些情况下,标记的核苷酸的聚合会向纳米孔呈现标签分子,其可以通过测量施加在纳米孔和/或膜上的多个电压的电流来鉴定。 本文还提供了用纳米孔对双链核酸分子的有义链和反义链进行测序的系统和方法,以及使用核糖核酸(RNA)速度突变分子来减缓核酸分子通过的方法或 靠近纳米孔。