Ensayo multiplex para Hepatitis B
    13.
    发明专利

    公开(公告)号:ES2711402T3

    公开(公告)日:2019-05-03

    申请号:ES14789058

    申请日:2014-04-25

    Abstract: Un kit que comprende: (a) un primer receptáculo que comprende: (i) perlas que se conjugan con antígeno de superficie de Hepatitis B (HBsAg) de humano y marcador detectable (i), (ii) perlas que se conjugan con antígeno de núcleo de Hepatitis B (HBcAg) de humano y marcador detectable (ii), y (iii) perlas que se conjugan con un anticuerpo específico para IgM (anti-IgM) de humano y marcador detectable (iii); (b) un segundo receptáculo que comprende (i) HBsAg biotinilado, y (ii) HBcAg biotinilado; y (c) un tercer receptáculo que comprende estreptavidina que se conjuga con un marcador detectable (iv).

    Dose surface method for determination of analyte ratios

    公开(公告)号:AU2011308657B2

    公开(公告)日:2014-12-18

    申请号:AU2011308657

    申请日:2011-09-30

    Abstract: Methods, systems, and apparatus for accurately determining a proportion (ratio) of two analytes is provided, as well as provide a concentration of a first analyte from a determined concentration of a second analyte and from a proportion of the analytes to each other. In one aspect, a surface model (called a dose surface herein) relating the concentrations of the two analytes to the proportion can be used to obtain accurate values for one of the variables (e.g. a concentration or the proportion) when the other two variables have previously been obtained. The dose surface can be a three-dimensional surface and be non-linear. The dose surface model can include multiple regression functions. For example, measured responses can be individually converted to concentrations using two dose-response curves, and the concentrations can be input to a dose surface function to obtain the proportion.

    Recombinant deamidated gliadin antigen

    公开(公告)号:AU2017272223B2

    公开(公告)日:2019-05-09

    申请号:AU2017272223

    申请日:2017-12-06

    Abstract: The present invention provides a method for determining whether a subject is suffering from celiac disease by contacting a sample of bodily fluid from the subject, with an antigen formed from a hexamer of a gliadin fusion protein immobilized on a solid support. The gliadin fusion protein of the antigen includes a recombinant deamidated gliadin linked to a tag such as Glutathione-S transferase (GST) protein. The antigen is prepared by immobilizing the gliadin fusion protein on the solid support. The antigen can further include tissue Transglutaminase (tTG) cross-linked to the gliadin fusion protein. When tTG is present, the tTG and recombinant deamidated gliadin are mixed together prior to immobilization to the solid phase. 9765390_1 (GHMatters) P97180.AU.1

    Recombinant deamidated gliadin antigen

    公开(公告)号:AU2017272223A1

    公开(公告)日:2018-01-04

    申请号:AU2017272223

    申请日:2017-12-06

    Abstract: The present invention provides a method for determining whether a subject is suffering from celiac disease by contacting a sample of bodily fluid from the subject, with an antigen formed from a hexamer of a gliadin fusion protein immobilized on a solid support. The gliadin fusion protein of the antigen includes a recombinant deamidated gliadin linked to a tag such as Glutathione-S transferase (GST) protein. The antigen is prepared by immobilizing the gliadin fusion protein on the solid support. The antigen can further include tissue Transglutaminase (tTG) cross-linked to the gliadin fusion protein. When tTG is present, the tTG and recombinant deamidated gliadin are mixed together prior to immobilization to the solid phase. 9765390_1 (GHMatters) P97180.AU.1

    Recombinant deamidated gliadin antigen

    公开(公告)号:AU2012348122B2

    公开(公告)日:2017-09-14

    申请号:AU2012348122

    申请日:2012-12-03

    Abstract: The present invention provides a method for determining whether a subject is suffering from celiac disease by contacting a sample of bodily fluid from the subject, with an antigen formed from a hexamer of a gliadin fusion protein immobilized on a solid support. The gliadin fusion protein of the antigen includes a recombinant deamidated gliadin linked to a tag such as Glutathione-S transferase (GST) protein. The antigen is prepared by immobilizing the gliadin fusion protein on the solid support. The antigen can further include tissue Transglutaminase (tTG) cross-linked to the gliadin fusion protein. When tTG is present, the tTG and recombinant deamidated gliadin are mixed together prior to immobilization to the solid phase.

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