METHOD FOR DETERMINATION OF PROGRESSION RISK OF GLAUCOMA
    3.
    发明申请
    METHOD FOR DETERMINATION OF PROGRESSION RISK OF GLAUCOMA 有权
    用于确定GLAUCOMA进程风险的方法

    公开(公告)号:US20110207122A1

    公开(公告)日:2011-08-25

    申请号:US12596462

    申请日:2008-04-17

    IPC分类号: C12Q1/68 C07H21/04

    摘要: A method of determining the presence or the absence of a glaucoma risk, including the steps of detecting in vitro an allele and/or a genotype of a single nucleotide polymorphism which is located on a 31st base of a base sequence, in a sample from a subject, wherein the base sequence is at least one base sequence selected from the group consisting of base sequences shown in SEQ ID NOs: 203 to 752 or a complementary sequence thereto (step A), and comparing the allele and/or the genotype detected in the step A with at least one of an allele and/or a genotype, containing a high-risk allele, in the base sequences shown in SEQ ID NOs: 203 to 752 (step B). According to the method of the present invention, the level of a progressive risk of glaucoma in a sample donor can be determined by analyzing an allele or a genotype of a single nucleotide polymorphism in the present invention in the sample, so that the sample donor can take a preventive measure of glaucoma, or can receive appropriate treatments, on the basis of this risk.

    摘要翻译: 一种确定青光眼风险的存在或不存在的方法,包括以下步骤:在位于碱基序列的第31位的单核苷酸多态性的体外检测等位基因和/或基因型, 其中所述碱基序列是选自SEQ ID NO:203至752所示的碱基序列或其互补序列的至少一种碱基序列(步骤A),并比较检测到的等位基因和/或基因型 在SEQ ID NO:203〜752(步骤B)所示的碱基序列中具有含有高风险等位基因的等位基因和/或基因型中的至少一种的步骤A。 根据本发明的方法,可以通过分析样品中本发明的单核苷酸多态性的等位基因或基因型来确定样品供体中青光眼进行性风险的水平,使得样品供体可以 采取预防措施的青光眼,或者可以根据这种风险接受适当的治疗。

    METHOD FOR DETERMINATION OF PROGRESSION RISK OF GLAUCOMA
    5.
    发明申请
    METHOD FOR DETERMINATION OF PROGRESSION RISK OF GLAUCOMA 审中-公开
    用于确定GLAUCOMA进程风险的方法

    公开(公告)号:US20130210668A1

    公开(公告)日:2013-08-15

    申请号:US13850453

    申请日:2013-03-26

    IPC分类号: C12Q1/68

    摘要: A method of determining the presence or the absence of a glaucoma risk, including the steps of detecting in vitro an allele and/or a genotype of a single nucleotide polymorphism which is located on a 31st base of a base sequence, in a sample from a subject, wherein the base sequence is at least one base sequence selected from the group consisting of base sequences shown in SEQ ID NOs: 203 to 752 or a complementary sequence thereto (step A), and comparing the allele and/or the genotype detected in the step A with at least one of an allele and/or a genotype, containing a high-risk allele, in the base sequences shown in SEQ ID NOs: 203 to 752 (step B). According to the method of the present invention, the level of a progressive risk of glaucoma in a sample donor can be determined by analyzing an allele or a genotype of a single nucleotide polymorphism in the present invention in the sample, so that the sample donor can take a preventive measure of glaucoma, or can receive appropriate treatments, on the basis of this risk.

    摘要翻译: 一种确定青光眼风险的存在或不存在的方法,包括以下步骤:在位于碱基序列的第31位的单核苷酸多态性的体外检测等位基因和/或基因型, 其中所述碱基序列是选自SEQ ID NO:203至752所示的碱基序列或其互补序列的至少一种碱基序列(步骤A),并比较检测到的等位基因和/或基因型 在SEQ ID NO:203〜752(步骤B)所示的碱基序列中具有含有高风险等位基因的等位基因和/或基因型中的至少一种的步骤A。 根据本发明的方法,可以通过分析样品中本发明的单核苷酸多态性的等位基因或基因型来确定样品供体中青光眼进行性风险的水平,使得样品供体可以 采取预防措施的青光眼,或者可以根据这种风险接受适当的治疗。

    Immunoassay method and reagent therefor
    6.
    发明授权
    Immunoassay method and reagent therefor 有权
    免疫测定法及其试剂

    公开(公告)号:US07759072B2

    公开(公告)日:2010-07-20

    申请号:US11817515

    申请日:2006-03-02

    IPC分类号: G01N33/53

    摘要: The present invention provides a novel immunoassay method with high reaction specificity and high sensitivity. The present invention also provides a method for immunoassaying a target antigen utilizing reactivation of an apoenzyme, which includes simultaneously or sequentially adding a test sample to an antibody specific to the target antigen, the target antigen labeled with a coenzyme, an apo-D-amino acid oxidase, a D-amino acid, and a reagent for detecting a hydrogen peroxide produced by the oxidase.

    摘要翻译: 本发明提供了具有高反应特异性和高灵敏度的新型免疫测定方法。 本发明还提供了使用辅酶的再活化来免疫测定靶抗原的方法,其包括同时或依次将测试样品加入到靶抗原特异性抗体中,用辅酶标记的靶抗原,载脂蛋白-D-氨基 酸性氧化酶,D-氨基酸和用于检测由氧化酶产生的过氧化氢的试剂。

    Inspecting method, inspecting system, and method for manufacturing electronic devices
    9.
    发明授权
    Inspecting method, inspecting system, and method for manufacturing electronic devices 有权
    检查方法,检查系统和电子设备制造方法

    公开(公告)号:US08428336B2

    公开(公告)日:2013-04-23

    申请号:US11431709

    申请日:2006-05-11

    IPC分类号: G06K9/00

    摘要: A method for classifying defects, including: calculating feature quantifies of defect image which is obtained by imaging a defect on a sample; classifying the defect image into a classified category by using information on the calculated feature quantities; displaying the classified defect image in a region on a display screen which is defined to the classified category; adding information on the classified category to the displayed defect image; transferring the displayed defect image which is added the information on the classified category to one of the other categories and displaying the transferred defect image in a region on the display screen which is defined to the one of the other categories; and changing information on the category.

    摘要翻译: 一种用于对缺陷进行分类的方法,包括:通过对样品上的缺陷进行成像而获得的缺陷图像的特征量化计算; 通过使用关于计算的特征量的信息将缺陷图像分类成分类的类别; 在分类的类别的显示屏幕上的区域中显示分类的缺陷图像; 将分类类别的信息添加到所显示的缺陷图像; 将所述分类类别中的信息添加到所述其他类别中的所显示的缺陷图像,并且将所传送的缺陷图像显示在所述显示屏幕上定义为所述其他类别之一的区域中; 并更改关于该类别的信息。

    METHOD FOR DETERMINATION OF ONSET RISK OF GLAUCOMA
    10.
    发明申请
    METHOD FOR DETERMINATION OF ONSET RISK OF GLAUCOMA 审中-公开
    确定葡萄球菌风险的方法

    公开(公告)号:US20130012408A1

    公开(公告)日:2013-01-10

    申请号:US13546674

    申请日:2012-07-11

    IPC分类号: C40B30/04 C12Q1/68

    摘要: A method of determining the presence or the absence of a glaucoma risk by detecting in vitro an allele and/or a genotype of a single nucleotide polymorphism, comparing the allele and/or the genotype detected with at least one of an allele and/or a genotype with a high-risk allele, wherein the presence of a glaucoma risk is determined in a case where the allele detected is the high-risk allele, or the presence of a glaucoma risk is determined in a case where the genotype detected is a homozygote of the genotype comprising the high-risk allele or a heterozygote when the high-risk allele complies with a dominant genetic model, or the presence of a glaucoma risk is determined in a case where the genotype detected is a homozygote of the genotype comprising the high-risk allele when the high-risk allele complies with a recessive genetic model.

    摘要翻译: 通过体外检测单核苷酸多态性的等位基因和/或基因型来确定青光眼存在或不存在青光眼风险的方法,比较检测到的等位基因和/或基因型与等位基因和/或 具有高风险等位基因的基因型,其中在检测到的等位基因是高风险等位基因的情况下确定青光眼风险的存在,或者在检测到的基因型是纯合子的情况下确定青光眼风险的存在 在高风险等位基因符合显性遗传模型的情况下,包括高风险等位基因或杂合子的基因型的基因型,或者在检测到的基因型是包含高表达的基因型的纯合子的情况下,确定青光眼风险的存在 当高风险等位基因符合隐性遗传模型时,这种等位基因是错误的。