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    • 4. 发明申请
    • HIGH THROUGHPUT GENE ASSEMBLY IN DROPLETS
    • 高渗透基因组装在DROPLETS
    • US20150361423A1
    • 2015-12-17
    • US14486346
    • 2014-09-15
    • Agilent Technologies, Inc.
    • Jeffrey R. SampsonNicholas M. Sampas
    • C12N15/10
    • C12N15/1093C12N15/1075
    • Provided herein is a method comprising: (a) obtaining a mixture of multiple sets of oligonucleotides, wherein the oligonucleotides within each set each comprise a terminal indexer sequence and can be assembled to produce a synthon; and (b) hybridizing the oligonucleotide mixture to an array, thereby spatially-separating the different sets of oligonucleotides from one another. In some embodiments the method may comprise (c) contacting the array with a solution, thereby producing, for each feature bound by the oligonucleotides, a discrete droplet comprising the feature and, optionally, placing an immiscible liquid over the droplets, thereby producing, for each feature bound by the oligonucleotides, a discrete reaction chamber defined by a droplet. The method may further comprise incubating the array under conditions by which a synthon is assembled in each of the reaction chambers. Other embodiments are also provided.
    • 本文提供的方法包括:(a)获得多组寡核苷酸的混合物,其中每组中的寡核苷酸各自包含末端分子序列,并且可以组装以产生合成子; 和(b)将寡核苷酸混合物与阵列杂交,从而将不同组的寡核苷酸彼此空间分离。 在一些实施方案中,该方法可以包括(c)使阵列与溶液接触,从而为由寡核苷酸结合的每个特征产生包含特征的离散液滴,并且任选地将不混溶液体放置在液滴上,从而产生 由寡核苷酸结合的每个特征,由液滴限定的离散反应室。 该方法还可以包括在每个反应室中组合合成子的条件下孵育该阵列。 还提供了其他实施例。