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    • 101. 发明授权
    • Methods for detecting nucleic acids by ligation of multiple oligomers
    • 通过连接多个寡聚体来检测核酸的方法
    • US06020138A
    • 2000-02-01
    • US241979
    • 1999-02-02
    • Hashem Akhavan-Tafti
    • Hashem Akhavan-Tafti
    • C12N15/10C12Q1/68C07H21/04C12P19/34
    • C12N15/10C12Q1/6827
    • Methods of synthesizing polynucleotides are disclosed involving the simultaneous ligation of a set of oligomer 5'-phosphates onto a template-bound primer. The set of these oligomers can be preselected to contain oligomers which are complementary to the template strand or the oligomers can be supplied as a library and allowed to self select. The synthesis by ligation can proceed unidirectionally or bidirectionally from the primer and can be used to synthesize both strands simultaneously by the use of two primers. The ligation is preferably performed with a ligase enzyme. The methods of synthesis are useful in a variety of applications, including cloning, amplification, labeling, diagnostic assays, mutation analysis and screening, gene expression monitoring and sequence analysis.
    • 公开了合成多核苷酸的方法,其涉及将一组低聚物5'-磷酸酯同时连接到模板结合的引物上。 这些低聚物的一组可以预选为含有与模板链互补的寡聚物,或者可以将寡聚物作为文库提供并允许自我选择。 通过连接的合成可以从引物单向或双向进行,并且可以通过使用两种引物同时合成两条链。 连接优选用连接酶进行。 合成方法可用于各种应用,包括克隆,扩增,标记,诊断测定,突变分析和筛选,基因表达监测和序列分析。
    • 102. 发明授权
    • Methods of synthesizing and amplifying polynucleotides by ligation of
multiple oligomers
    • 通过多个寡聚体的连接合成和扩增多核苷酸的方法
    • US05998175A
    • 1999-12-07
    • US121887
    • 1998-07-24
    • Hashem Akhavan-Tafti
    • Hashem Akhavan-Tafti
    • C12N15/10C12Q1/68C07H21/04C12P19/34
    • C12N15/10C12Q1/6827
    • Methods of synthesizing polynucleotides are disclosed involving the simultaneous ligation of a set of oligomer 5'-phosphates onto a template-bound primer. The set of these oligomers can be preselected to contain oligomers which are complementary to the template strand or the oligomers can be supplied as a library and allowed to self select. The synthesis by ligation can proceed unidirectionally or bidirectionally from the primer and can be used to synthesize both strands simultaneously by the use of two primers. The ligation is preferably performed with a ligase enzyme. The methods of synthesis are useful in a variety of applications, including cloning, amplification, labeling, diagnostic assays, mutation analysis and screening, gene expression monitoring and sequence analysis.
    • 公开了合成多核苷酸的方法,其涉及将一组低聚物5'-磷酸酯同时连接到模板结合的引物上。 这些低聚物的一组可以预选为含有与模板链互补的寡聚物,或者可以将寡聚物作为文库提供并允许自我选择。 通过连接的合成可以从引物单向或双向进行,并且可以通过使用两种引物同时合成两条链。 连接优选用连接酶进行。 合成方法可用于各种应用,包括克隆,扩增,标记,诊断测定,突变分析和筛选,基因表达监测和序列分析。
    • 106. 发明授权
    • Acridan compounds
    • 吖啶化合物
    • US5670644A
    • 1997-09-23
    • US647383
    • 1996-05-09
    • Hashem Akhavan-TaftiZahra ArghavaniRenuka DeSilva
    • Hashem Akhavan-TaftiZahra ArghavaniRenuka DeSilva
    • C07D219/02C07D219/04C07D219/06C12Q1/28C07D285/38C07D295/00G01N33/532G01N33/533
    • C07D219/02C07D219/04C07D219/06C12Q1/28
    • A chemiluminescent assay method, compositions, kits and chemiluminescent acridan compounds are described which use a two-step chemiluminescent reaction process. The reaction involves an acridan compound, preferably a derivative of an N-alkylacridan-9-carboxylic acid, which undergoes a reaction with a peroxide compound, a peroxidase enzyme and an enhancer under conditions of time, temperature and pH which permit the accumulation of an intermediate compound, which is subsequently induced to produce a burst of light by raising the pH. The result is generation of very high intensity light from the reaction. The peroxidase enzyme is present alone or linked to a member of a specific binding pair in an immunoassay, DNA probe assay or other assay where the hydrolytic enzyme is bound to a reporter molecule. The method is particularly amenable to automated assays because of the separation of the incubation and light generating steps.
    • 描述了使用两步化学发光反应过程的化学发光测定方法,组合物,试剂盒和化学发光的吖啶化合物。 该反应涉及吖啶化合物,优选N-烷基吖啶-9-羧酸的衍生物,其在时间,温度和pH条件下与过氧化物,过氧化物酶和增强剂发生反应,这允许积聚 中间体化合物,其随后通过提高pH而被诱导产生突发性的光。 结果是从反应产生非常高强度的光。 过氧化物酶在免疫测定,DNA探针测定或其他测定中单独存在或连接到特异性结合对的成员,其中水解酶与报道分子结合。 由于孵育和光生成步骤的分离,该方法特别适用于自动化测定。