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    • 68. 发明申请
    • SISO MODEL PREDICTIVE CONTROLLER
    • SISO模型预测控制器
    • WO2005077038A2
    • 2005-08-25
    • PCT/US2005004011
    • 2005-02-04
    • WISCONSIN ALUMNI RES FOUND
    • G05B13/02G05B13/04
    • G05B13/048
    • A method of predictive control for a single input, single output (SISO) system, including modeling the SISO system with model factors, detecting output from the SISO system, estimating a filtered disturbance from the output, determining a steady state target state from the filtered disturbance and a steady state target output, populating a dynamic optimization solution table using the model factors and a main tuning parameter, and determining an optimum input from the dynamic optimization solution table. Determining an optimum input includes determining a time varying parameter, determining a potential optimum input from the time varying parameter, and checking, whether the potential optimum input is the optimum input.
    • 一种用于单输入单输出(SISO)系统的预测控制方法,包括用模型因子对SISO系统进行建模,检测SISO系统的输出,从输出估计滤波后的干扰,从滤波器确定稳态目标状态 干扰和稳态目标输出,使用模型因子和主调优参数填充动态优化解表,并从动态优化解决方案表确定最优输入。 确定最佳输入包括确定时变参数,根据时变参数确定潜在最佳输入,以及检查潜在最佳输入是否是最佳输入。
    • 69. 发明申请
    • METHOD AND COMPOSITIONS FOR DETECTING BOTULINUM NEUROTOXIN
    • 用于检测嗜碱性神经毒素的方法和组合物
    • WO2005076785A2
    • 2005-08-25
    • PCT/US2004042366
    • 2004-12-20
    • WISCONSIN ALUMNI RES FOUNDCHAPMAN EDWIN RDONG MIN
    • CHAPMAN EDWIN RDONG MIN
    • C07K14/435G01N33/542G01N33/569
    • G01N33/573C07K14/435C07K14/43595C07K14/705C07K2319/50C07K2319/60C12Y304/24069G01N33/542G01N33/56911G01N2333/33G01N2333/952
    • A molecular construct capable of fluorescent resonance energy transfer (FRET), comprising a linker peptide, a donor fluorophore moiety and an acceptor fluorophore moiety, wherein the linker peptide is a substrate of a botulinum neurotoxin selected from the group consisting of synaptobrevin, syntaxin and SNAP-25, or a fragment thereof capable being cleaved by the botulinum neurotoxin, and separates the donor and acceptor fluorophores by a distance of not more than 10 nm, and wherein emission spectrum of the donor fluorophore moiety overlaps with the excitation spectrum of the acceptor fluorophore moiety; or wherein the emission spectra of the fluorophores are detectably different. Also provided are isolated nucleic acid expressing the construct, kits comprising said construct and cell lines comprising said nucleic acid. Further provided are methods of detecting a BoNT using the above described construct via FRET, and methods for detecting a BoNT using surface plasmon resonance imaging.
    • 一种能够进行荧光共振能量转移(FRET)的分子构建体,其包含接头肽,供体荧光团部分和受体荧光团部分,其中所述连接肽是肉毒神经毒素的底物,其选自突触链突起目,突触蛋白和突触蛋白 -25或其能够被肉毒杆菌神经毒素切割的片段,并且将供体和受体荧光团分开不超过10nm的距离,并且其中供体荧光团部分的发射光谱与受体荧光团的激发光谱重叠 部分; 或其中荧光团的发射光谱可检测地不同。 还提供了表达构建体的分离的核酸,包含所述构建体的试剂盒和包含所述核酸的细胞系。 还提供了通过FRET使用上述构建体检测BoNT的方法,以及使用表面等离子体共振成像检测BoNT的方法。