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    • 1. 发明授权
    • Methods and device for DNA sequencing using surface enhanced raman scattering (SERS)
    • 使用表面增强拉曼散射(SERS)进行DNA测序的方法和装置
    • US07476501B2
    • 2009-01-13
    • US10108128
    • 2002-03-26
    • Selena ChanXing SuTae-Woong Koo
    • Selena ChanXing SuTae-Woong Koo
    • C12Q1/68
    • C12Q1/6869B01L3/5027C12Q2565/60C12Q2565/631C12Q2565/632G01N21/658G01N33/587G01N2021/653G01N2021/656
    • The methods and apparatus disclosed herein concern nucleic acid sequencing by enhanced Raman spectroscopy. In certain embodiments of the invention, exonuclease treatment of the nucleic acids 109 results in the release of nucleotides 110. The nucleotides may pass from a reaction chamber 101 through a microfluidic channel 102 and enter a nanochannel or microchannel 103. The nanochannel or microchannel 103 may be packed with nanoparticle 111 aggregates containing hot spots for Raman detection. As the nucleotides 110 pass through the nanoparticle 111 hot spots, they may be detected by surface enhanced Raman spectroscopy (SERS), surface enhanced resonance Raman spectroscopy (SERRS) and/or coherent anti-Stokes Raman spectroscopy (CARS). Identification of the sequence of nucleotides 110 released from the nucleic acid 109 provides the nucleic acid sequence. Other embodiments of the invention concern apparatus 100 for nucleic acid sequencing.
    • 本文公开的方法和装置涉及通过增强拉曼光谱进行的核酸测序。 在本发明的某些实施方案中,核酸109的核酸外切酶处理导致核苷酸110的释放。核苷酸可以从反应室101通过微流体通道102并进入纳米通道或微通道103.纳米通道或微通道103可以 填充含有用于拉曼检测的热点的纳米颗粒111聚集体。 当核苷酸110通过纳米颗粒111热点时,它们可以通过表面增强拉曼光谱(SERS),表面增强共振拉曼光谱(SERRS)和/或相干抗斯托克斯拉曼光谱(CARS)来检测。 从核酸109释放的核苷酸序列110的鉴定提供了核酸序列。 本发明的其它实施方案涉及用于核酸测序的设备100。
    • 2. 发明授权
    • Detecting molecular binding by monitoring feedback controlled cantilever deflections
    • 通过监测反馈控制的悬臂偏转来检测分子结合
    • US07105301B2
    • 2006-09-12
    • US10667776
    • 2003-09-22
    • Xing SuSelena ChanTae-Woong KooMineo YamakawaAndrew A. Berlin
    • Xing SuSelena ChanTae-Woong KooMineo YamakawaAndrew A. Berlin
    • C12Q1/68C12Q1/70G01N33/566G01N33/563
    • C12Q1/6825B82Y5/00G01N33/54373G01N2800/52Y10S977/924C12Q2565/501
    • The present methods and apparatus concern the detection and/or identification of target analytes using probe molecules. In various embodiments of the invention, the probes or analytes are attached to one or more cantilevers. Binding of a probe to an analyte results in deflection of the cantilever, detected by a detection unit. A counterbalancing force may be applied to restore the cantilever to its original position. The counterbalancing force may be magnetic, electrical or radiative. The detection unit and the mechanism generating the counterbalancing force may be operably coupled to an information processing and control unit, such as a computer. The computer may regulate a feedback loop that maintains the cantilever in a fixed position by balancing the deflecting force and the counterbalancing force. The concentration of analytes in a sample may be determined from the magnitude of the counterbalancing force required to maintain the cantilever in a fixed position.
    • 本方法和装置涉及使用探针分子检测和/或鉴定目标分析物。 在本发明的各种实施方案中,探针或分析物附着到一个或多个悬臂。 将探针与分析物结合导致由检测单元检测到的悬臂的偏转。 可以应用平衡力将悬臂恢复到其原始位置。 平衡力可以是磁性的,电的或辐射的。 生成平衡力的检测单元和机构可以可操作地耦合到诸如计算机的信息处理和控制单元。 计算机可以通过平衡偏转力和平衡力来调节将悬臂维持在固定位置的反馈回路。 样品中分析物的浓度可以从将悬臂维持在固定位置所需的平衡力的大小来确定。