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    • 1. 发明授权
    • Modular capillary bridge viscometer
    • US09612183B2
    • 2017-04-04
    • US13825623
    • 2011-09-23
    • Paul G. ClarkeMichael P. Murphy
    • Paul G. ClarkeMichael P. Murphy
    • G01N11/08
    • G01N11/08
    • A capillary bridge viscometer (120), comprises at least two at least generally balanced bridge arm conduits (R1, R2) a bulkhead supporting structure (122,134) supporting removable connection portions for each of a plurality of the arms in a bridge configuration, a bridge supporting structure (124,136) supporting the bridge arm conduits (R1,R2) and supporting two further removable connection portions (132) for each of the bridge arm conduits, wherein each of the further removable connection portions (132) supported by the bridge supporting structure are positioned to mate with a corresponding one of the removable connection portions (130) supported by the bulkhead supporting structure concurrently to hydraulically connect the bridge arm conduits in the bridge configuration; and a balance detector having hydraulic connections for connection between first and second differential detection points in the bridge when the removable connection portions on the bridge are mated to corresponding ones of the removable connection portions supported by the bulkhead supporting structure.
    • 2. 发明申请
    • MODULAR CAPILLARY BRIDGE VISCOMETER
    • 模块化毛细管粘度计
    • US20140060162A1
    • 2014-03-06
    • US13825623
    • 2011-09-23
    • Paul G. ClarkeMichael P. Murphy
    • Paul G. ClarkeMichael P. Murphy
    • G01N11/08
    • G01N11/08
    • A capillary bridge viscometer (120), comprises at least two at least generally balanced bridge arm conduits (R1, R2) a bulkhead supporting structure (122,134) supporting removable connection portions for each of a plurality of the arms in a bridge configuration, a bridge supporting structure (124,136) supporting the bridge arm conduits (R1,R2) and supporting two further removable connection portions (132) for each of the bridge arm conduits, wherein each of the further removable connection portions (132) supported by the bridge supporting structure are positioned to mate with a corresponding one of the removable connection portions (130) supported by the bulkhead supporting structure concurrently to hydraulically connect the bridge arm conduits in the bridge configuration; and a balance detector having hydraulic connections for connection between first and second differential detection points in the bridge when the removable connection portions on the bridge are mated to corresponding ones of the removable connection portions supported by the bulkhead supporting structure.
    • 一种毛细管桥式粘度计(120),包括至少两个至少大体上平衡的桥臂导管(R1,R2),隔板支撑结构(122,134),其以桥式结构支撑多个臂中的每一个的可移除连接部分, 支撑结构(124,136),其支撑桥臂导管(R1,R2),并为每个桥臂导管支撑两个另外的可移除的连接部分(132),其中每个所述另外可移除的连接部分(132)由所述桥梁支撑结构 定位成与由隔板支撑结构支撑的可拆卸连接部分(130)同时配合以使桥臂配置中的桥臂管道液压连接; 以及具有液压连接的平衡检测器,当桥上的可移除连接部分与由隔板支撑结构支撑的相应的可拆卸连接部分配合时,在桥中的第一和第二差动检测点之间进行连接。
    • 9. 发明申请
    • Method for Generating Reference Controls for Pharmacogenomic Testing
    • 生成药物基因组检测参考控制的方法
    • US20090197945A1
    • 2009-08-06
    • US12162199
    • 2007-01-29
    • Michael P. MurphyScott L. ClarkPamela J. NakhleKenneth G. Butz
    • Michael P. MurphyScott L. ClarkPamela J. NakhleKenneth G. Butz
    • C12Q1/68A61K31/352A61P3/00A61P9/00A61P25/00A61P35/00A61P37/00
    • C12N5/0635C12N2503/00C12N2510/04
    • Reference controls for use with pharmacogenomic testing, and methods for their identification, preparation, and use, are disclosed. The reference controls can confirm that pharmacogenomic testing correctly identifies individuals that do or do not have the mutation of interest, in both clinical trial and patient treatment settings. The reference controls can be selected to include one or more mutations to be identified, and prescreened to confirm that they bind to one or more of the primers used in the pharmacogenomic testing. The reference controls are human genomic DNA that includes certain identified polymorphisms (mutations) of interest, ideally derived from individuals, pre-selected and optionally properly consented, which have one or more of the polymorphism(s) of interest. The reference controls can be prepared by targeted pre-screening of human patients, by examining the genotype or genetic profile of the patients, isolating cells with the desired mutation, optionally immortalizing the cells, and obtaining DNA from the cells. The prescreening of prospective donors can be targeted based on any of a number of factors, such as genes of interest, mutations within the genes of interest, and membership in a specific ethnic or disease state population. The genomic DNA can be pre-screened for its ability to be detected, using a standard pharmacogenomic test, as including a specific mutation. Examples of mutations of interest include those present in a Phase I or Phase II metabolic enzyme such as CYP2D6, CYP2C19, CYP2C9, CYP2C8, and CYP3A5, CYP3A4, CYP2A6, CYP2B6, UGT1A1, DPD, ERCC1, MDR1, ADH2, NAT1 and NAT2 or any other metabolic or disease gene.
    • 公开了用于药物基因组测试的参考对照及其鉴定,制备和使用的方法。 在临床试验和患者治疗环境中,参照对照可以证实药物基因组检测正确地识别出有或没有感兴趣突变的个体。 可以选择参考对照以包括待鉴定的一个或多个突变,并进行预筛选以确认它们与药物基因组测试中使用的一种或多种引物结合。 参考对照是人基因组DNA,其包括某些鉴定的目的多态性(突变),理想地衍生自预先选择的和任选正确同意的个体,其具有一个或多个感兴趣的多态性。 通过检查患者的基因型或遗传概况,分离具有所需突变的细胞,任选地使细胞永生化,以及从细胞中获得DNA,可以通过靶向预筛选人类患者来制备参照对照。 可以基于许多因素,如感兴趣的基因,感兴趣的基因内的突变以及特定种族或疾病状态群体的成员中的任何一个因素来预先预先筛选前瞻性供体。 可以使用标准药物基因组测试将基因组DNA的筛选能力进行预筛选,作为包括特异性突变。 感兴趣的突变的实例包括存在于I期或II期代谢酶如CYP2D6,CYP2C19,CYP2C9,CYP2C8和CYP3A5,CYP3A4,CYP2A6,CYP2B6,UGT1A1,DPD,ERCC1,MDR1,ADH2,NAT1和NAT2中的那些, 任何其他代谢或疾病基因。