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    • 8. 发明授权
    • PCR process and arrangement for DNA amplification using dry reagents
    • 使用干试剂进行DNA扩增的PCR过程和排列
    • US07993828B2
    • 2011-08-09
    • US11587567
    • 2005-04-26
    • Walter GumbrechtPeter PaulickaManfred Stanzel
    • Walter GumbrechtPeter PaulickaManfred Stanzel
    • C12Q1/68
    • C12Q1/686
    • A PCR process for DNA amplification with thermocyclisation of the corresponding reagents is disclosed, in which total integration of all substances and process steps is achieved in a closed, single-use unit (so-called cartridge) in which the reagents are stored in a storage-stable form at room temperature. According to the process, the water-soluble reagents are covered by a water-insoluble medium, then the DNA to be amplified is supplied and the water-insoluble medium is eliminated, so that the water-soluble reagents are dissolved and PCR can start. In the corresponding arrangement, a test unit designed as a single-use produce (a so-called cartridge) has at least one micro-channel or micro-cavity for receiving a PCR reagent. The PCR reagents in the form of a mixture which can be dried at a negligible vapour pressure and forms a storage-stable substance substance at room temperature adhere to the walls of the micro-channel or micro-cavity and form a thin film covered by an insoluble medium.
    • 公开了用于相应试剂的热循环的DNA扩增的PCR方法,其中所有物质和方法步骤的完全整合在封闭的一次性使用单元(所谓的盒)中实现,其中试剂存储在储存器 - 稳定形式在室温下。 根据该方法,水溶性试剂被水不溶性介质覆盖,然后供给待扩增的DNA,除去水不溶性介质,溶解水溶性试剂并开始PCR。 在相应的布置中,设计为单次使用的产品(所谓的盒)的测试单元具有用于接收PCR试剂的至少一个微通道或微腔。 可以以可忽略的蒸气压干燥并在室温下形成储存稳定物质物质的混合物形式的PCR试剂粘附到微通道或微腔的壁上并形成由 不溶性介质。