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    • 1. 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℃。
    • 3. 发明申请
    • 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
    • US20110014673A1
    • 2011-01-20
    • US12835822
    • 2010-07-14
    • Kyle W. HukariJason A.A. West
    • Kyle W. HukariJason A.A. West
    • C12N13/00C12N5/00C12M1/02
    • 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. 发明申请
    • PCR-FREE SAMPLE PREPARATION AND DETECTION SYSTEMS FOR HIGH SPEED BIOLOGIC ANALYSIS AND IDENTIFICATION
    • 用于高速生物分析和鉴定的无PCR样品制备和检测系统
    • US20100216657A1
    • 2010-08-26
    • US12301099
    • 2007-05-16
    • Kyle Wisdom HukariJason Andrew Appleton WestDustin LiBrent Coleman SatterfieldLars L. Majlof
    • Kyle Wisdom HukariJason Andrew Appleton WestDustin LiBrent Coleman SatterfieldLars L. Majlof
    • C40B30/04C40B40/06
    • G01N21/6428B01L3/0275B01L3/502715B01L3/502761B01L2300/0636G01N21/6456G01N2021/6482G01N2035/00158
    • Provided herein are biologic sample preparation and analysis systems that are rapid, portable, robust detection system for multiplexed detection of bio-threats, and which can be ruggedized to operate in harsh environments. A new method of detection called Combinatorial Probe Analysis (CPA), which provides an exponential increase in detection reliability, has been incorporated into these systems. This type of analysis greatly reduces false positives and false negatives; in addition it is reusable and eliminates special storage requirements for reagents. Specific technical advancements in the optimization of hybridization assays for nucleic acid detection on porous polymer monoliths (PPM) are also disclosed. Performing rapid and complete solubilization of viruses, vegetative bacteria and bacterial spores with an ultra high temperature solubilization protocol is also described. The systems provided herein provides the ability to perform rapid highly multiplexed analysis of a variety of bioagents, including bacteria viruses, and protein biotoxins. The systems and assays described herein are perform completely automated sample preparation and analysis, in a time frame of five minutes or less. The assay is simple in design allowing users in personal protective equipment to easily operate the system. The disclosed systems are robust, simple to use, and address the goals of the first responder community.
    • 本文提供了生物样品制备和分析系统,其是用于多重检测生物威胁的快速,便携,鲁棒的检测系统,并且其可以坚固地在恶劣环境中操作。 称为组合探测分析(CPA)的一种新的检测方法,其检测可靠性提高了指数增长,已被纳入这些系统。 这种分析大大减少了假阳性和假阴性; 此外,它是可重复使用的,并且消除了对试剂的特殊储存要求。 还公开了在多孔聚合物整料(PPM)上的核酸检测的杂交测定的优化中的具体技术进步。 还描述了用超高温溶解方案快速和完全地溶解病毒,营养细菌和细菌孢子。 本文提供的系统提供对多种生物代谢物进行快速高度多重分析的能力,包括细菌病毒和蛋白质生物毒素。 本文所述的系统和测定在五分钟或更短的时间内执行完全自动化的样品制备和分析。 该测定设计简单,允许个人防护设备中的用户轻松操作系统。 所公开的系统是健壮的,易于使用的,并且解决了第一响应者社区的目标。