会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 52. 发明申请
    • METHODS FOR ELECTROCHEMICAL DETECTION/QUANTIFICATION OF A NUCLEIC ACID
    • 一种核酸的电化学检测/定量方法
    • US20100133117A1
    • 2010-06-03
    • US12376782
    • 2006-08-08
    • Zhiqiang Gao
    • Zhiqiang Gao
    • C12Q1/28
    • G01N27/447C12Q1/6825C12Q2525/107C12Q2533/101C12Q2525/101
    • The invention provides methods and kits for the electrochemical detection and/or quantification of a target nucleic acid molecule by means of a detection electrode. In one method there is immobilized on the detection electrode a peptide nucleic acid (PNA) capture molecule, which has a nucleotide sequence that is at least partially complementary to at least a portion of the target nucleic acid molecule. The electrode is contacted with a solution expected to include the target nucleic acid molecule and the target nucleic acid molecule allowed to hybridize to the PNA, thereby allowing the formation of a complex between the PNA capture molecule and the target nucleic acid molecule. A polymerisable positively chargeable precursor is added, which associates to the complex formed between the PNA capture molecule and the target nucleic acid molecule. A suitable reactant molecule is added, initiating the polymerisation of the polymerisable positively chargeable precursor and the formation of an electroconductive polymer. An electrochemical measurement at the detection electrode is performed. In another method a nucleic acid capture molecule is immobilized on the electrode. In this method a polymerisable positively chargeable precursor, a suitable substrate molecule, and an enzyme attached to a detection probe nucleic acid molecule are used. The detection probe nucleic acid molecule is at least partially complementary to at least a portion of the target nucleic acid molecule. The detection probe hybridizes to a portion of the target nucleic acid that is different from the portion to which the capture nucleic acid molecule hybridises.
    • 本发明提供了用于通过检测电极电化学检测和/或定量靶核酸分子的方法和试剂盒。 在一种方法中,固定在检测电极上的肽核酸(PNA)捕获分子,其具有与目标核酸分子的至少一部分至少部分互补的核苷酸序列。 使电极与预期包含靶核酸分子和允许与PNA杂交的靶核酸分子的溶液接触,从而允许在PNA捕获分子和靶核酸分子之间形成复合物。 加入可聚合的带正电荷的前体,其与PNA捕获分子和靶核酸分子之间形成的复合物相关联。 加入合适的反应物分子,引发可聚合的可带正电荷的前体和形成导电聚合物。 进行检测电极的电化学测定。 在另一种方法中,核酸捕获分子固定在电极上。 在该方法中,使用可聚合的可带正电荷的前体,合适的底物分子和附着于检测探针核酸分子的酶。 检测探针核酸分子与靶核酸分子的至少一部分至少部分互补。 检测探针与靶核酸的不同于捕获核酸分子杂交的部分杂交。
    • 58. 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。
    • 60. 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。