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    • 5. 发明申请
    • REAL-TIME PCR MICROARRAY BASED ON AN EVANESCENT WAVE BIOSENSOR
    • 基于EVANESCENT WAV生物传感器的实时PCR微波
    • WO2006135437A9
    • 2007-05-18
    • PCT/US2005037833
    • 2005-10-21
    • HONEYWELL INT INCXU LIANG
    • XU LIANG
    • C12Q1/68
    • G06N3/02H04L67/12H04L69/329
    • A system and method for simultaneous, quantitative measurement of nucleic acids in a sample. Fluorescently tagged amplicons of the target nucleic acids are localized on a substrate surface by hybridization to oligopobes that have been arrayed and tethered to the substrate surface in a pre-determined, two-dimensional pattern. The hybridized, amplicons are then detected by exciting their fluorescent tags using an evanescent wave flight of the appropriate wave-length. Because of the limited penetration of the evanescent wave (about 100-300 nm), the fluorescently tagged nucleotides in the remainder of the reaction cell do not fluoresce. By measuring the fluorescence at various locations on the substrate surface, the current abundance of hybridized amplicons of each of the target nucleic acids can be determined. The analytic techniques of real time PCR may then be used to obtain accurate, quantitative measurements for each of the nucleic acids in the sample.
    • 用于同时,定量测量样品中核酸的系统和方法。 通过与已经以预定的二维图案排列和束缚到基底表面的寡核苷酸杂交,将目标核酸的荧光标记的扩增子定位在底物表面上。 然后通过使用适当波长的ev逝波飞行激发其荧光标签来检测杂交的扩增子。 由于ev逝波(约100-300nm)的穿透有限,反应池其余部分的荧光标记核苷酸不发荧光。 通过测量底物表面上各个位置的荧光,可以确定每个目标核酸的杂交扩增子的当前丰度。 然后可以使用实时PCR的分析技术来获得样品中每个核酸的准确,定量的测量。
    • 9. 发明申请
    • REAL-TIME PCR MICROARRAY BASED ON AN EVANESCENT WAVE BIOSENSOR
    • 基于EVANESCENT WAVE BIOSENSOR的实时PCR微阵列
    • WO2006135437A3
    • 2007-04-05
    • PCT/US2005037833
    • 2005-10-21
    • HONEYWELL INT INCXU LIANG
    • XU LIANG
    • C12Q1/68
    • G06N3/02H04L67/12H04L69/329
    • A system and method for simultaneous, quantitative measurement of nucleic acids in a sample. Fluorescently tagged amplicons of the target nucleic acids are localized on a substrate surface by hybridization to oligopobes that have been arrayed and tethered to the substrate surface in a pre-determined, two-dimensional pattern. The hybridized, amplicons are then detected by exciting their fluorescent tags using an evanescent wave flight of the appropriate wave-length. Because of the limited penetration of the evanescent wave (about 100-300 nm), the fluorescently tagged nucleotides in the remainder of the reaction cell do not fluoresce. By measuring the fluorescence at various locations on the substrate surface, the current abundance of hybridized amplicons of each of the target nucleic acids can be determined. The analytic techniques of real time PCR may then be used to obtain accurate, quantitative measurements for each of the nucleic acids in the sample.
    • 用于同时定量测量样品中核酸的系统和方法。 靶核酸的荧光标记的扩增子通过与已经以预定的二维图案排列并连接到基底表面的寡聚体杂交而定位在基底表面上。 然后通过使用适当波长的eva逝波飞行激发它们的荧光标签来检测杂交的扩增子。 由于渐逝波(约100-300nm)的有限穿透,反应池剩余部分中荧光标记的核苷酸不发荧光。 通过测量底物表面上不同位置处的荧光,可以确定每种靶核酸的杂交扩增子的电流丰度。 然后可以使用实时PCR的分析技术来获得样品中每种核酸的精确的定量测量结果。