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    • 2. 发明授权
    • Systems and methods for effecting a physical change in a biological sample
    • 影响生物样品物理变化的系统和方法
    • US08450095B2
    • 2013-05-28
    • US12835822
    • 2010-07-14
    • Kyle W. HukariJason A. A. West
    • Kyle W. HukariJason A. A. West
    • C12N13/00
    • C12N13/00C12M47/06
    • The present invention relates generally to systems and methods for processing a biological sample that result in a physical change, such as reacting two molecules together to form a reaction product or for use in lysing viruses or biological cells for analysis using biological assay systems. As such, the present invention relates both to breaking apart biological species such as viruses and cells, as well as the formation of reactants from one or more reactive species. The sample has a volume in the range from about 1 microliter to 10 milliliters. The sample is processed by applying pressure, and either sonic energy or thermal energy to the sample, wherein the pressure achieved is usually at least 24 atmospheres, and the temperature of the sample is usually raised to at least 50° C.
    • 本发明一般涉及用于处理导致物理变化的生物样品的系统和方法,例如将两个分子一起反应以形成反应产物或用于裂解病毒或生物细胞用于使用生物测定系统进行分析。 因此,本发明涉及分解生物物种如病毒和细胞,以及从一种或多种反应性物质形成反应物。 样品的体积在约1微升至10毫升的范围内。 通过对样品施加压力和声能或热能来处理样品,其中获得的压力通常为至少24个大气压,并且样品的温度通常升高至至少50℃。
    • 4. 发明授权
    • Systems and methods for effecting a physical change in a biological sample
    • 影响生物样品物理变化的系统和方法
    • US07781206B2
    • 2010-08-24
    • US11402656
    • 2006-04-11
    • Kyle W. HukariJason A. A. West
    • Kyle W. HukariJason A. A. West
    • C12M1/00
    • C12N13/00C12M47/06
    • The present invention relates generally to systems and methods for processing a biological sample that result in a physical change, such as reacting two molecules together to form a reaction product or for use in lysing viruses or biological cells for analysis using biological assay systems. As such, the present invention relates both to breaking apart biological species such as viruses and cells, as well as the formation of reactants from one or more reactive species. The sample has a volume in the range from about 1 microliter to 10 milliliters. The sample is processed by applying pressure, and either sonic energy or thermal energy to the sample, wherein the pressure achieved is usually at least 24 atmospheres, and the temperature of the sample is usually raised to at least 50° C.
    • 本发明一般涉及用于处理导致物理变化的生物样品的系统和方法,例如将两个分子一起反应以形成反应产物或用于裂解病毒或生物细胞用于使用生物测定系统进行分析。 因此,本发明涉及分解生物物种如病毒和细胞,以及从一种或多种反应性物质形成反应物。 样品的体积在约1微升至10毫升的范围内。 通过对样品施加压力和声能或热能来处理样品,其中获得的压力通常为至少24个大气压,并且样品的温度通常升高至至少50℃。
    • 9. 发明授权
    • Universal probe assay methods
    • 通用探针测定方法
    • US09353406B2
    • 2016-05-31
    • US13280214
    • 2011-10-24
    • Kenneth J. LivakJason A. A. WestRobert C. Jones
    • Kenneth J. LivakJason A. A. WestRobert C. Jones
    • C12Q1/68
    • C12Q1/682C12Q1/6876C12Q2600/178C12Q2525/155C12Q2525/307C12Q2537/161
    • Reagents and methods are provided for detecting the presence of a target polynucleotide in a sample are disclosed. In one aspect, a method for producing a labeled amplification product by amplifying a target nucleic acid sequence to produce an amplification product comprising the target sequence, a first probe-binding sequence 5′ to the target sequence, and a second probe-binding sequence 3′ to the target sequence, thereby producing an amplification product; and hybridizing a first detection probe to the amplification product, the first detection probe comprising a first segment that hybridizes to the first probe-binding sequence and a second segment that hybridizes to the second probe-binding sequence, thereby producing a labeled amplification product is disclosed.
    • 提供了用于检测样品中靶多核苷酸的存在的试剂和方法。 一方面,通过扩增靶核酸序列以产生包含靶序列的扩增产物,与靶序列的第一探针结合序列5'和第二探针结合序列3来产生标记的扩增产物的方法 '到靶序列,从而产生扩增产物; 并且将第一检测探针与扩增产物杂交,所述第一检测探针包含与第一探针结合序列杂交的第一区段和与第二探针结合序列杂交的第二区段,从而产生标记的扩增产物 。