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    • 55. 发明申请
    • METHOD FOR DE NOVO DETECTION OF SEQUENCES IN NUCLEIC ACIDS: TARGET SEQUENCING BY FRAGMENTATION
    • 在核酸中检测序列的方法:通过分段进行的目标序列
    • US20090075288A1
    • 2009-03-19
    • US12259376
    • 2008-10-28
    • Charles R. CantorFouad A. Siddiqi
    • Charles R. CantorFouad A. Siddiqi
    • C12Q1/68
    • C12Q1/6872C12Q2525/101C12Q2523/107
    • The present invention provides a method for determining nucleic acid sequences of a template nucleic acid that requires no prior knowledge of the nucleic acid sequence present in the template nucleic acid. The method is based on combining information about the mass of a fragment, the mass of any one nucleotide and the combinations thereof, and the sequence specificity of a nucleotide cutter, either enzymatic or chemical cutter, to determine a sequence of a nucleic acid fragment. This method allows for de novo detection of sequences in a target nucleic acid without requiring any prior sequence information. This method is called Partial Sequencing by Fragmentation (PSBF) and it works by fragmenting a target into oligo- or polynucleotides whose masses or lengths are uniquely associated with known sequences. The identities of these sequences are determined solely by the specific fragmentation method used, and are always independent of the target. PSBF can be implemented using electrophoresis, mass spectrometry or any other method that can be used to distinguish the size of the cut nucleic acid sequence fragments.
    • 本发明提供了一种确定模板核酸的核酸序列的方法,其不需要模板核酸中存在的核酸序列的先验知识。 该方法基于组合关于片段的质量,任何一个核苷酸的质量及其组合的信息以及核苷酸切割剂(酶或化学切割机)的序列特异性,以确定核酸片段的序列。 该方法允许从头检测靶核酸中的序列,而不需要任何先前的序列信息。 这种方法被称为通过片段化分段测序(PSBF),它的作用是通过将目标片段分成其质量或长度与已知序列唯一相关的寡核苷酸或多核苷酸。 这些序列的身份完全由所使用的具体碎片方法确定,并且始终与目标无关。 PSBF可以使用电泳,质谱法或可用于区分切割的核酸序列片段的大小的任何其它方法来实现。
    • 57. 发明授权
    • Methods for detection and quantification of analytes in complex mixtures
    • 复杂混合物中分析物的检测和定量方法
    • US07473767B2
    • 2009-01-06
    • US09898743
    • 2001-07-03
    • Krassen Dimitrov
    • Krassen Dimitrov
    • C07H21/04C12Q1/68
    • C12Q1/6888C12Q1/6816C12Q1/682C12Q1/6876C12Q2565/102C12Q2537/143C12Q2525/161C12Q2565/1025C12Q2563/179C12Q2525/151C12Q2525/101
    • The invention provides a diverse population of uniquely labeled probes, containing about thirty or more target specific nucleic acid probes each attached to a unique label bound to a nucleic acid. Also provided is a method of producing a population of uniquely labeled nucleic acid probes. The method consists of (a) synthesizing a population of target specific nucleic acid probes each having a different specifier; (b) synthesizing a corresponding population of anti-genedigits each having a unique label, the population having a diversity sufficient to uniquely hybridize to genedigits within the specifiers, and (c) hybridizing the populations of target nucleic acid probes to the anti-genedigits, to produce a population in which each of the target specific probes is uniquely labeled. Also provided is a method of detecting a nucleic acid analyte.
    • 本发明提供了多种独特标记的探针,其含有约30个或更多个目标特异性核酸探针,其各自附着于与核酸结合的唯一标记。 还提供了生产独特标记的核酸探针群体的方法。 该方法包括(a)合成具有不同说明符的目标特异性核酸探针群; (b)合成各自具有独特标记的相应抗原基因群体,所述群体具有足以独特地与指定物内的基因组杂交的多样性,和(c)将靶核酸探针的群体与抗Genieigits杂交, 以产生其中每个靶特异性探针被唯一标记的群体。 还提供了检测核酸分析物的方法。