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    • 61. 发明公开
    • BIOMARKERS FOR GASTRIC CANCER AND USES THEREOF
    • BIOMARKERFÜRMAGENKREBS UND VERWENDUNGEN DAVON
    • EP2805167A4
    • 2015-12-09
    • EP13738133
    • 2013-01-17
    • ADELAIDE RES & INNOVATION PTY
    • HOFFMANN PETERPENNO MEGANERNST MATTHIAS ROBERT WALTER
    • G01N33/574C12Q1/68
    • G01N33/57446C12Q1/6886C12Q2600/112C12Q2600/136C12Q2600/158C12Q2600/16G01N33/5023G01N33/57488G01N33/92G01N2333/65G01N2333/76G01N2333/775G01N2333/811G01N2800/52G01N2800/60
    • The present invention provides biological markers associated with gastric cancer. In particular, the present invention provides a method of diagnosing gastric cancer (GC) in a subject, the method including: measuring an expression level of one or more proteins in the subject, wherein the one or more proteins are selected from the group consisting of vitamin D binding protein (VDBP), clusterin, insulin like growth factor binding protein complex acid labile subunit (IGFALS), and afamin; comparing the expression level of the or each protein in the subject to a reference expression level for the or each protein; and diagnosing GC in the subject on the basis of the comparison. On the basis of the identification of biological markers associated with gastric cancer, the present invention also provides a method of determining if a subject is susceptible to developing gastric cancer, a method of assessing progression of gastric cancer in a subject, a method for screening a candidate therapeutic agent useful for treating gastric cancer in a subject, and a kit for diagnosing gastric cancer in a subject.
    • 本发明提供与胃癌相关的生物标志物。 特别地,本发明提供了一种诊断受试者胃癌(GC)的方法,所述方法包括:测量受试者中一种或多种蛋白质的表达水平,其中所述一种或多种蛋白质选自 维生素D结合蛋白(VDBP),聚集蛋白,胰岛素样生长因子结合蛋白复合酸不稳定亚基(IGFALS)和微生物; 将受试者中的每种蛋白质的表达水平与该蛋白质或每种蛋白质的参考表达水平进行比较; 并根据比较诊断受试者的GC。 本发明基于与胃癌相关的生物标志物的鉴定,还提供了确定受试者是否易于发生胃癌的方法,评估受试者胃癌进展的方法,筛选方法 可用于治疗受试者胃癌的候选治疗剂和用于诊断受试者胃癌的试剂盒。
    • 62. 发明公开
    • Method for the detection of the prozone effect of photometric assays
    • Verfahren zur Bestimmung der Prozonwirkung von photometrischen Assays
    • EP2837937A1
    • 2015-02-18
    • EP13180560.8
    • 2013-08-15
    • Roche Diagnostics GmbHF. Hoffmann-La Roche AG
    • Garbulewska, EwelinaKurz, GeorgLopez-Calle, EloisaRoedl, Josef
    • G01N33/53
    • G01N33/557G01N33/5306G01N2333/76
    • The invention provides a method for determination of the amount of a specific analyte in a sample which may show a prozone effect by photometric assays, wherein the specific analyte is quantified from the change in the optical signal of the reaction mixture after the interaction of the analyte with analyte specific assay reagents. The optical signal is measured simultaneously for the specific analyte in the sample to be determined at the wavelength used for the determination of the analyte and at least at an additional specific wavelength used for the detection of the prozone effect over the complete reaction time. The reaction rate ratio R is calculated by using the signals obtained at the wavelength used for the detection of the prozone effect. By comparison of the calculated ratio value R with predetermined limit values it is judged if a prozone effect is present in the sample.
    • 本发明提供了一种用于测定样品中特定分析物的量的方法,其可以通过光度测定显示前区效应,其中特异性分析物在分析物相互作用之后从反应混合物的光学信号的变化中量化 与分析物特异性测定试剂。 同时测量样品中用于测定分析物的波长确定的特定分析物的光学信号,并至少在用于在完整反应时间内检测前区效应的另外的特定波长。 通过使用在用于检测前区效应的波长处获得的信号来计算反应速率比R. 通过将计算的比值R与预定极限值进行比较,判断样品中是否存在前区效应。
    • 66. 发明公开
    • DETECTOR AND DETECTION METHOD
    • DETEKTOR UND NACHWEISVERFAHREN
    • EP2418485A1
    • 2012-02-15
    • EP09843017.6
    • 2009-04-09
    • Hitachi Chemical Company, Ltd.
    • HIGUCHI, MasayukiNAKANO, YuuichiSUZUKI, NahokoNAKAMURA, MikiYAMASHITA, Kouhei
    • G01N33/543
    • G01N33/558G01N33/6854G01N2333/76
    • Provided is a strip-shaped detector that detects an analyte in a liquid sample. The detector includes a collecting member that directly collects a liquid sample from a living organism, a holding member that holds a labeling reagent binding specifically to the analyte in a state where the labeling reagent can move along with the movement of the liquid sample, a detecting member to which a detection reagent is immobilized which captures a complex of the analyte and the labeling reagent by binding specifically to the analyte, an absorbing member that can absorb the liquid sample, and a liquid-impermeable supporting member, wherein the respective members are arranged on the supporting member in the longitudinal direction of the detector so that the liquid sample moves through the inside of these members, and the collecting member includes a protruding portion sticking out of the supporting member at the upstream side in the movement direction of the liquid sample.
    • 提供了一种检测液体样品中的分析物的条形检测器。 检测器包括:收集构件,其从活体直接收集液体样品;保持构件,其保持在标记试剂可随着液体样品的移动而移动的状态下特异性结合分析物的标记试剂;检测 固定有检测试剂的成员,其通过特异性结合分析物捕获分析物和标记试剂的复合物,可吸收液体样品的吸收构件和液体不可渗透的支撑构件,其中各构件布置 在检测器的纵向方向上的支撑构件上,使得液体样品通过这些构件的内部移动,并且收集构件包括在液体样品的移动方向上游侧的支撑构件伸出的突出部分 。
    • 69. 发明公开
    • D/P CREATININE MARKER, METHOD OF DETERMINING D/P CREATININE AND USE OF THE SAME
    • D / P-KREATINMARKER,VERFAHREN ZUM BESTIMMEN VON D / P-KREATIN UND VERWENDUNG DAVON
    • EP2051080A1
    • 2009-04-22
    • EP07807873.0
    • 2007-09-26
    • JMS Co., Ltd.
    • HIRAI, SatoshiKARINO, Tomokazu
    • G01N33/70
    • G01N33/70G01N2333/76
    • A method of indirectly determining D/P creatinine for easily judging a peritoneal function is provided that does not require blood sampling or multiple recoveries of dialysis effluent. The method includes preparing a dialysis effluent obtained by peritoneal dialysis, measuring at least one protein marker selected from the group consisting of prealbumin, haptoglobin, alpha 1-microglobulin, C4, and total protein that are contained in the dialysis effluent, and determining D/P creatinine indirectly from the correlation equation that represents the relationship between the marker concentration and the D/P creatinine value that has been prepared beforehand. Furthermore, the PET category is determined indirectly from the D/P creatinine, which has been determined indirectly, based on the known reference value.
    • 提供间接测定D / P肌酐以容易判断腹膜功能的方法,其不需要血液取样或多次回收透析流出物。 该方法包括制备通过腹膜透析获得的透析流出物,测量至少一种选自透析流出物中包含的前白蛋白,触珠蛋白,α1-微球蛋白,C4和总蛋白质的蛋白质标记物,并测定D / P肌酸酐间接地代表了事先准备的标记浓度与D / P肌酐值之间关系的相关方程。 此外,PET类别是根据已知参考值间接测定的D / P肌酸酐间接测定的。