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    • 1. 发明授权
    • Turning center with integrated non-contact inspection system
    • 车削中心配有非接触式检测系统
    • US06233533B1
    • 2001-05-15
    • US09090087
    • 1998-06-04
    • Hong XuDonald Lee Burgoon
    • Hong XuDonald Lee Burgoon
    • G06F770
    • G01R31/343G01R31/302
    • A non-contact inspection system has one or more pairs of non-contact sensors, pointing at the braking surfaces and a non-contact sensor pointing at the outer diameter of a disc. The non-contact sensors can be inductive sensors, capacitive probes and/or laser sensors. A controller is connected to each sensor for signal processing and measurement output. The system measures various features and characteristics, such as braking surface thickness variation, lateral run-out, flatness, parallelism and diameters. Measurements are made while the disc rotates at a specified speed or while the disc is stationary. The pairs of non-contact sensors continuously measure the distance from the sensor or calibrated surface to the pointed surface. Thereby the run-out and thickness variations can be calculated from the measurements at different radii. By combining the measurements on the same braking surface, the flatness and parallelism are calculated. The other two sensors continuously measure the distance from the sensor or the calibrated surface to the pointed surface. A diameter can be calculated knowing the center of the disc. The lateral run-out, thickness variation, flatness and parallelism can be measured on each brake disc within the turning center for final inspection and/or statistical process control. The diameter measurement and its run-out can be fed back to the turning center to monitor and compensate tool wear.
    • 非接触检查系统具有指向制动表面的一对或多对非接触传感器和指向盘的外径的非接触式传感器。 非接触式传感器可以是电感式传感器,电容式探头和/或激光传感器。 控制器连接到每个传感器用于信号处理和测量输出。 该系统测量制动表面厚度变化,侧向跳动,平直度,平行度和直径等各种特征和特点。 当盘以特定速度旋转或盘静止时进行测量。 这些非接触传感器对连续测量从传感器或校准表面到尖面的距离。 因此,可以从不同半径的测量计算出偏差和厚度变化。 通过将相同制动表面上的测量结合在一起,计算平面度和平行度。 另外两个传感器连续地测量从传感器或校准表面到尖面的距离。 可以计算知道光盘中心的直径。 可以在车削中心内的每个制动盘上测量横向偏移,厚度变化,平直度和平行度,以进行最终检查和/或统计过程控制。 直径测量及其跳动可以反馈到车削中心,以监测和补偿刀具磨损。
    • 7. 发明申请
    • Methods of Cationic Polymer Detection
    • 阳离子聚合物检测方法
    • US20120270328A1
    • 2012-10-25
    • US13119295
    • 2010-12-21
    • Guixi ZhangSijing WangHong XuXiaofeng Tang
    • Guixi ZhangSijing WangHong XuXiaofeng Tang
    • G01N21/49
    • G01N21/49
    • The present invention concerns a method of detecting cationic polymers comprising: obtaining a target water sample containing a cationic polymer; adding a polymer dispersant solution and a phosphate solution to the target water sample, the polymer dispersant solution is comprised of a polymer dispersant with calcium and magnesium hardness and the phosphate solution is comprised of a phosphate; standing the target water sample; and measuring the turbidity of the target water sample; comparing the turbidity of said target water sample with a calibration curve of the turbidity of samples containing known concentrations of cationic polymers to determine the concentration of cationic polymers in said target water sample.
    • 本发明涉及一种检测阳离子聚合物的方法,包括:获得含有阳离子聚合物的目标水样品; 将聚合物分散剂溶液和磷酸盐溶液加入到目标水样品中,聚合物分散剂溶液由具有钙和镁硬度的聚合物分散剂组成,磷酸盐溶液由磷酸盐组成; 站在目标水样上; 并测量目标水样品的浊度; 将所述目标水样品的浊度与含有已知浓度的阳离子聚合物的样品的浊度的校准曲线进行比较,以确定所述目标水样品中阳离子聚合物的浓度。
    • 8. 发明授权
    • In vitro methods of detecting cells sensitive to sweet tastants by detecting expression of hetero-oligomeric T1R2/T1R3 taste receptors
    • 通过检测异低聚T1R2 / T1R3味觉受体的表达来检测对甜味滋味物敏感的细胞的体外方法
    • US08206938B2
    • 2012-06-26
    • US13099327
    • 2011-05-02
    • Mark ZollerXiaodong LiLena StaszewskiShawn O'ConnellSergey ZozulyaJon Elliot AdlerHong XuFernando Echeverri
    • Mark ZollerXiaodong LiLena StaszewskiShawn O'ConnellSergey ZozulyaJon Elliot AdlerHong XuFernando Echeverri
    • G01N33/53G01N33/567C12Q1/68
    • G01N33/5041A01K2217/05C07K14/705C07K2319/00C12Q1/6876C12Q2600/124C12Q2600/158G01N33/5008G01N33/566G01N2333/4719G01N2333/705G01N2333/726G01N2500/04
    • The present invention relates to the discovery that the T1R receptors assemble to form functional taste receptors. Particularly, it has been discovered that co-expression of T1R1 and T1R3 results in a taste receptor that responds to umami taste stimuli, including monosodium glutamate. Also, it has been discovered that co-expression of the T1R2 and T1R3 receptors results in a taste receptor that responds to sweet taste stimuli including naturally occurring and artificial sweeteners.Also the present invention relates to the use of hetero-oligomeric taste receptors comprising T1R1/T1R3 and T1R2/T1R3 in assays to identify compounds that respectively respond to umami taste stimuli and sweet taste stimuli.Further, the invention relates to the constitutive of cell lines that stably or transiently co-express a combination of T1R1 and T1R3; or T1R2 and T1R3; under constitutive or inducible conditions. The use of these cells lines in cell-based assays to identify umami and sweet taste modulatory compounds is also provided, particularly high throughput screening assays that detect receptor activity by use of fluorometric imaging.Finally, the invention relates to the discovery that some compounds, e.g., lactisole, inhibit both the activities of human T1R2/T1R3 and T1R1/T1R3 receptors, and accordingly the sweet and umami taste, suggesting that these receptors may be the only sweet and umami receptors.
    • 本发明涉及T1R受体组装形成功能性味觉受体的发现。 特别地,已经发现,T1R1和T1R3的共表达导致对鲜味刺激(包括谷氨酸钠)起反应的味觉感受器。 此外,已经发现,T1R2和T1R3受体的共表达导致对包括天然存在的和人造甜味剂的甜味刺激有反应的味觉受体。 本发明还涉及在测定中使用包含T1R1 / T1R3和T1R2 / T1R3的异低聚味觉感受器来鉴定分别响应于鲜味刺激和甜味刺激的化合物。 此外,本发明涉及稳定或瞬时共表达T1R1和T1R3的组合的细胞系的组成; 或T1R2和T1R3; 在组成型或诱导性条件下。 还提供了在基于细胞的测定中使用这些细胞系以鉴定鲜味和甜味调节化合物,特别是通过使用荧光成像检测受体活性的高通量筛选测定。 最后,本发明涉及一些发现,一些化合物,例如乳酸,抑制人T1R2 / T1R3和T1R1 / T1R3受体的活性,因此抑制甜味和鲜味,这表明这些受体可能是唯一的甜味和鲜味 受体。
    • 9. 发明授权
    • Methods of detecting T1R2- and T1R3-expressing cells potentially sensitive to sweet tastants
    • 检测对甜味滋味剂有潜在敏感性的T1R2-和T1R3表达细胞的方法
    • US08168401B2
    • 2012-05-01
    • US13023462
    • 2011-02-08
    • Mark ZollerXiaodong LiLena StaszewskiShawn O'ConnellSergey ZozulyaJon Elliot AdlerHong XuFemando Echeverri
    • Mark ZollerXiaodong LiLena StaszewskiShawn O'ConnellSergey ZozulyaJon Elliot AdlerHong XuFemando Echeverri
    • G01N33/53G01N33/567
    • G01N33/5041A01K2217/05C07K14/705C07K2319/00C12Q1/6876C12Q2600/124C12Q2600/158G01N33/5008G01N33/566G01N2333/4719G01N2333/705G01N2333/726G01N2500/04
    • The present invention relates to the discovery that the T1R receptors assemble to form functional taste receptors. Particularly, it has been discovered that co-expression of T1R1 and T1R3 results in a taste receptor that responds to umami taste stimuli, including monosodium glutamate. Also, it has been discovered that co-expression of the T1R2 and T1R3 receptors results in a taste receptor that responds to sweet taste stimuli including naturally occurring and artificial sweeteners.Also the present invention relates to the use of hetero-oligomeric taste receptors comprising T1R1/T1R3 and T1R2/T1R3 in assays to identify compounds that respectively respond to umami taste stimuli and sweet taste stimuli.Further, the invention relates to the constitutive of cell lines that stably or transiently co-express a combination of T1R1 and T1R3; or T1R2 and T1R3; under constitutive or inducible conditions. The use of these cells lines in cell-based assays to identify umami and sweet taste modulatory compounds is also provided, particularly high throughput screening assays that detect receptor activity by use of fluorometric imaging.Finally, the invention relates to the discovery that some compounds, e.g., lactisole, inhibit both the activities of human T1R2/T1R3 and T1R1/T1R3 receptors, and accordingly the sweet and umami taste, suggesting that these receptors may be the only sweet and umami receptors.
    • 本发明涉及T1R受体组装形成功能性味觉受体的发现。 特别地,已经发现,T1R1和T1R3的共表达导致对鲜味刺激(包括谷氨酸钠)起反应的味觉感受器。 此外,已经发现,T1R2和T1R3受体的共表达导致对包括天然存在的和人造甜味剂的甜味刺激有反应的味觉受体。 本发明还涉及在测定中使用包含T1R1 / T1R3和T1R2 / T1R3的异低聚味觉感受器来鉴定分别响应于鲜味刺激和甜味刺激的化合物。 此外,本发明涉及稳定或瞬时共表达T1R1和T1R3的组合的细胞系的组成; 或T1R2和T1R3; 在组成型或诱导性条件下。 还提供了在基于细胞的测定中使用这些细胞系以鉴定鲜味和甜味调节化合物,特别是通过使用荧光成像检测受体活性的高通量筛选测定。 最后,本发明涉及一些发现,一些化合物,例如乳酸,抑制人T1R2 / T1R3和T1R1 / T1R3受体的活性,因此抑制甜味和鲜味,这表明这些受体可能是唯一的甜味和鲜味 受体。