Immunoassays employing non-particulate chemiluminescent reagent
    1.
    发明授权
    Immunoassays employing non-particulate chemiluminescent reagent 有权
    免疫测定采用非微粒化学发光试剂

    公开(公告)号:US09347947B2

    公开(公告)日:2016-05-24

    申请号:US12403299

    申请日:2009-03-12

    IPC分类号: G01N21/76 G01N33/58

    摘要: Methods and reagents are disclosed for conducting assays. Embodiments of the present methods and reagents are concerned with chemiluminescent reagents for determining the presence and/or amount of an analyte in a sample suspected of containing the analyte. The reagent is non-particulate and comprises a binding partner for the analyte and a chemiluminescent composition comprising an olefinic compound and a metal chelate. In embodiments of an assay, a combination is provided that comprises a sample suspected of containing the analyte, a chemiluminescent reagent as described above and a sensitizer reagent capable of generating singlet oxygen. The combination is subjected to conditions for binding of the analyte to the binding partner for the analyte. The sensitizer is activated and the amount of luminescence generated by the chemiluminescent composition is detected wherein the amount of luminescence is related to the amount of the analyte in the sample.

    摘要翻译: 公开了用于进行测定的方法和试剂。 本发明方法和试剂的实施方案涉及用于确定怀疑含有分析物的样品中分析物的存在和/或量的化学发光试剂。 试剂是非颗粒的并且包含用于分析物的结合配偶体和包含烯属化合物和金属螯合物的化学发光组合物。 在测定的实施方案中,提供了包含疑似含有分析物的样品,如上所述的化学发光试剂和能够产生单线态氧的敏化剂的组合。 该组合经受用于将分析物与分析物的结合配偶体结合的条件。 敏化剂被激活,并且检测由化学发光组合物产生的发光量,其中发光量与样品中分析物的量相关。

    IMMUNOASSAYS EMPLOYING NON-PARTICULATE CHEMILUMINESCENT REAGENT
    2.
    发明申请
    IMMUNOASSAYS EMPLOYING NON-PARTICULATE CHEMILUMINESCENT REAGENT 有权
    免费使用非颗粒性发光试剂

    公开(公告)号:US20100233725A1

    公开(公告)日:2010-09-16

    申请号:US12403299

    申请日:2009-03-12

    IPC分类号: G01N33/53

    摘要: Methods and reagents are disclosed for conducting assays. Embodiments of the present methods and reagents are concerned with chemiluminescent reagents for determining the presence and/or amount of an analyte in a sample suspected of containing the analyte. The reagent is non-particulate and comprises a binding partner for the analyte and a chemiluminescent composition comprising an olefinic compound and a metal chelate. In embodiments of an assay, a combination is provided that comprises a sample suspected of containing the analyte, a chemiluminescent reagent as described above and a sensitizer reagent capable of generating singlet oxygen. The combination is subjected to conditions for binding of the analyte to the binding partner for the analyte. The sensitizer is activated and the amount of luminescence generated by the chemiluminescent composition is detected wherein the amount of luminescence is related to the amount of the analyte in the sample.

    摘要翻译: 公开了用于进行测定的方法和试剂。 本发明方法和试剂的实施方案涉及用于确定怀疑含有分析物的样品中分析物的存在和/或量的化学发光试剂。 试剂是非颗粒的并且包含用于分析物的结合配偶体和包含烯属化合物和金属螯合物的化学发光组合物。 在测定的实施方案中,提供了包含疑似含有分析物的样品,如上所述的化学发光试剂和能够产生单线态氧的敏化剂的组合。 该组合经受用于将分析物与分析物的结合配偶体结合的条件。 敏化剂被激活,并且检测由化学发光组合物产生的发光量,其中发光量与样品中分析物的量相关。

    Immunoassays for buprenorphine and norbuprenorphine
    5.
    发明授权
    Immunoassays for buprenorphine and norbuprenorphine 有权
    丁丙诺啡和诺布啡诺的免疫测定

    公开(公告)号:US07220842B2

    公开(公告)日:2007-05-22

    申请号:US10818115

    申请日:2004-04-05

    CPC分类号: C07K16/44 G01N33/9486

    摘要: Methods, compositions and kits are disclosed directed at haptens, immunogens and immunoassays for buprenorphine (BUP) and nor buprenorphine (norBUP). The method comprises providing in combination in a medium (i) a sample suspected of containing buprenorphine (BUP) or norbuprenorphine (norBUP) and (ii) an antibody raised against an immunogen of buprenorphine (BUP) or norbuprenorphine (norBUP). The medium is examined for the presence of a complex comprising a labeled hapten of buprenorphine (BUP) or norbuprenorphine (norBUP) where the presence of such as complex indicates the presence of the compound in the sample.

    摘要翻译: 公开了针对丁丙诺啡(BUP)和丁丙诺啡(norBUP)的半抗原,免疫原和免疫测定法的方法,组合物和试剂盒。 该方法包括在介质中提供(i)怀疑含有丁丙诺啡(BUP)或降丁非诺(norBUP))的样品和(ii)针对丁丙诺啡(BUP)或去诺贝芬(norBUP)的免疫原产生的抗体。 检查介质是否存在包含丁丙诺啡(BUP)或降丁非诺(norBUP)的标记半抗原的复合物,其中诸如复合物的存在表明样品中存在化合物。

    Immunoassays for buprenorphine and norbuprenorphine
    6.
    发明申请
    Immunoassays for buprenorphine and norbuprenorphine 有权
    丁丙诺啡和诺布啡诺的免疫测定

    公开(公告)号:US20050221405A1

    公开(公告)日:2005-10-06

    申请号:US10818115

    申请日:2004-04-05

    IPC分类号: G01N33/53 G01N33/94

    CPC分类号: C07K16/44 G01N33/9486

    摘要: Methods, compositions and kits are disclosed directed at haptens, immunogens and immunoassays for buprenorphine (BUP) and nor buprenorphine (norBUP). The method comprises providing in combination in a medium (i) a sample suspected of containing buprenorphine (BUP) or norbuprenorphine (norBUP) and (ii) an antibody raised against an immunogen of buprenorphine (BUP) or norbuprenorphine (norBUP). The medium is examined for the presence of a complex comprising a labeled hapten of buprenorphine (BUP) or norbuprenorphine (norBUP) where the presence of such as complex indicates the presence of the compound in the sample.

    摘要翻译: 公开了针对丁丙诺啡(BUP)和丁丙诺啡(norBUP)的半抗原,免疫原和免疫测定法的方法,组合物和试剂盒。 该方法包括在介质中提供(i)怀疑含有丁丙诺啡(BUP)或降丁非诺(norBUP))的样品和(ii)针对丁丙诺啡(BUP)或去诺贝芬(norBUP)的免疫原产生的抗体。 检查介质是否存在包含丁丙诺啡(BUP)或降丁非诺(norBUP)的标记半抗原的复合物,其中诸如复合物的存在表明样品中存在化合物。

    Reducing Non-Specifically Bound Molecules on Supports
    7.
    发明申请
    Reducing Non-Specifically Bound Molecules on Supports 审中-公开
    减少支架上的非特异性结合分子

    公开(公告)号:US20140356885A1

    公开(公告)日:2014-12-04

    申请号:US13905459

    申请日:2013-05-30

    IPC分类号: G01N33/53

    CPC分类号: G01N33/54333

    摘要: Methods and reagents are disclosed for preparing a support for reaction of the support with an assay molecule. In the method the support is treated with a detergent at a concentration of about 0.01% to about 5% (by weight) at a temperature of about 4° C. to about 50° C. for a period of about 1 hour to about 24 hours and subsequently the support is washed. The support is contacted with the assay molecule under conditions for covalently binding the assay molecule to the support to form a conjugate of the support and the assay molecule.

    摘要翻译: 公开了用于制备载体与测定分子反应的载体的方法和试剂。 在该方法中,在约4℃​​至约50℃的温度下,以约0.01%至约5%(重量)的浓度的洗涤剂处理载体约1小时至约24 小时,随后洗涤支持。 在将分析分子共价结合到载体以形成载体和测定分子的缀合物的条件下,将支持物与测定分子接触。

    Immunoassays for buprenorphine and norbuprenorphine
    8.
    发明授权
    Immunoassays for buprenorphine and norbuprenorphine 有权
    丁丙诺啡和诺布啡诺的免疫测定

    公开(公告)号:US07863427B2

    公开(公告)日:2011-01-04

    申请号:US11734661

    申请日:2007-04-12

    IPC分类号: C07K17/02 C07D491/02

    CPC分类号: C07K16/44 G01N33/9486

    摘要: Methods, compositions and kits are disclosed directed at haptens, immunogens and immnoassays for buprenorphine (BUP) and nor buprenorphine (norBUP). The method comprises providing in combination in a medium (i) a sample suspected of containing buprenorphine (BUP) or norbuprenorphine (norBUP) and (ii) an antibody raised against an immunogen of buprenorphine (BUP) or norbuprenorphine (norBUP). The medium is examined for the presence of a complex comprising a labeled hapten of buprenorphine (BUP) or norbuprenorphine (norBUP) where the presence of such as complex indicates the presence of the compound in the sample.

    摘要翻译: 公开了针对丁丙诺啡(BUP)和丁丙诺啡(norBUP)的半抗原,免疫原和免疫测定法的方法,组合物和试剂盒。 该方法包括在介质中提供(i)怀疑含有丁丙诺啡(BUP)或降丁非诺(norBUP))的样品和(ii)针对丁丙诺啡(BUP)或去诺贝芬(norBUP)的免疫原产生的抗体。 检查介质是否存在包含丁丙诺啡(BUP)或降丁非诺(norBUP)的标记半抗原的复合物,其中诸如复合物的存在表明样品中存在化合物。

    Signal Ratio in Assay Calibrators
    9.
    发明申请
    Signal Ratio in Assay Calibrators 审中-公开
    测定校准物中的信号比

    公开(公告)号:US20140212987A1

    公开(公告)日:2014-07-31

    申请号:US13753909

    申请日:2013-01-30

    IPC分类号: G01N33/82

    摘要: Methods of enhancing signal ratio between calibrators in an assay for an analyte include conducting an assay for the analyte with zero concentration of analyte in a first calibrator to determine a first signal level. The reagents employed in the assay comprise an antibody reagent comprising an antibody for the analyte wherein a hinge region of the antibody is conjugated to a moiety. The assay for the analyte is also conducted with a second concentration of analyte in a second calibrator to determine a second signal level wherein the second analyte concentration is greater than zero and wherein the reagents employed in the assay comprise the antibody reagent. A ratio of the first signal level to the second signal level is determined and evaluated.

    摘要翻译: 在分析物测定中增强校准器之间的信号比率的方法包括在第一校准器中对零分析物进行分析物测定以确定第一信号水平。 在测定中使用的试剂包含抗体试剂,其包含用于分析物的抗体,其中抗体的铰链区域与部分缀合。 分析物的测定还用第二校准器中的第二浓度的分析物进行,以确定第二分析物浓度大于零的第二信号水平,并且其中测定中使用的试剂包含抗体试剂。 确定并评估第一信号电平与第二信号电平的比率。

    REDUCTION IN KICKBACK EFFECT IN COMPARATORS
    10.
    发明申请
    REDUCTION IN KICKBACK EFFECT IN COMPARATORS 有权
    在比较器中减少KICKBACK效应

    公开(公告)号:US20110032136A1

    公开(公告)日:2011-02-10

    申请号:US12512824

    申请日:2009-07-30

    IPC分类号: H03M1/12 H03K5/22

    CPC分类号: H03K3/356139 H03K3/013

    摘要: The present disclosure relates to reduction in the effect of kickback in comparators by means of charge injection implemented by means of voltage controlled switches with attributes similar to those of an input differential pair. The voltage controlled switches produce charge to neutralize the charge loss during latching of inputs in the comparator.

    摘要翻译: 本公开涉及通过借助于具有与输入差分对的属性类似的电压控制开关实现的电荷注入来减少比较器中反冲的影响。 电压控制开关产生电荷以中和比较器中的输入锁存期间的电荷损失。