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    • 7. 发明授权
    • Diagnostic kits for detection of target nucleic acid sequences
    • 用于检测靶核酸序列的诊断试剂盒
    • US5863732A
    • 1999-01-26
    • US769601
    • 1996-12-18
    • Rodney M. Richards
    • Rodney M. Richards
    • C12N15/10C12Q1/68C07H21/04C12P19/34
    • C12Q1/6853C12N15/10C12Q1/682C12Q1/6823Y02P20/582Y10S435/975
    • The present invention makes possible the catalytic production of sequence specific oligonucleotides through the use of a specially designed template sequence. The reaction can be made to proceed isothermally in the presence of an excess of nucleoside triphosphates, an agent for polymerization, and a cutting agent. Because the process is catalytic with respect to the template sequence, an unlimited amount of oligonucleotide product can theoretically be generated from a single molecule of template. Where the process is initiated by the presence of a nucleic acid target sequence, the method of the present invention can be used for diagnostic purposes as an amplification method to improve sensitivity. Diagnostic sensitivity can be further enhanced by employing a cascade of these template sequences.
    • 本发明通过使用特别设计的模板序列使得序列特异性寡核苷酸的催化生成成为可能。 反应可以在过量的核苷三磷酸,聚合剂和切割剂的存在下进行等温进行。 因为该方法对于模板序列是催化的,所以理论上可以从单个模板分子产生无限量的寡核苷酸产物。 当通过存在核酸靶序列引发该过程时,本发明的方法可用作诊断目的,作为增强灵敏度的扩增方法。 通过采用这些模板序列的级联可以进一步提高诊断灵敏度。
    • 8. 发明授权
    • Enzymatic synthesis of oligonucleotides
    • 寡核苷酸的酶合成
    • US5645987A
    • 1997-07-08
    • US200897
    • 1994-02-23
    • Rodney M. Richards
    • Rodney M. Richards
    • C12N15/10C12Q1/68C12P19/34
    • C12Q1/6853C12N15/10C12Q1/682C12Q1/6823Y02P20/582Y10S435/975
    • The present invention makes possible the catalytic production of sequence specific oligonucleotides through the use of a specially designed template sequence. The reaction can be made to proceed isothermally in the presence of an excess of nucleoside triphosphates, an agent for polymerization, and a cutting agent. Because the process is catalytic with respect to the template sequence, an unlimited amount of oligonucleotide product can theoretically be generated from a single molecule of template. Where the process is initiated by the presence of a nucleic acid target sequence, the method of the present invention can be used for diagnostic purposes as an amplification method to improve sensitivity. Diagnostic sensitivity can be further enhanced by employing a cascade of these template sequences.
    • 本发明通过使用特别设计的模板序列使得序列特异性寡核苷酸的催化生成成为可能。 反应可以在过量的核苷三磷酸,聚合剂和切割剂的存在下进行等温进行。 因为该方法对于模板序列是催化的,所以理论上可以从单个模板分子产生无限量的寡核苷酸产物。 当通过存在核酸靶序列引发该过程时,本发明的方法可用于诊断目的,作为增强灵敏度的扩增方法。 通过采用这些模板序列的级联可以进一步提高诊断灵敏度。