Human Anti-Herpes simplex virus Type 1 and 2 IgG ELISA Kit (HSV1+2) (ab108741)

Overview

  • Product nameHuman Anti-Herpes simplex virus Type 1 and 2 IgG ELISA Kit (HSV1+2)
  • Detection methodColorimetric
  • Precision
    Intra-assay
    Sample n Mean SD CV%
    Pos.Serum 13 5.8%
    Inter-assay
    Sample n Mean SD CV%
    Pos.Serum 3 3.6%
  • Tests
    1 x 96 test
  • Sample type
    Serum, Plasma
  • Assay typeIndirect
  • Assay durationMultiple steps standard assay
  • Species reactivity
    Reacts with: Human
  • Product overview

    Abcam’s anti-Herpes simplex virus Type 1 and 2 (HSV1+2) IgG Human in vitro ELISA (Enzyme-Linked Immunosorbent Assay) kit is designed for the accurate qualitative measurement of IgG class antibodies against Herpes simplex virus Type 1 and 2 in Human serum and plasma.

    A 96-well plate has been precoated with Herpes simplex virus Type 1 and 2 antigens to bind cognate antibodies. Controls or test samples are added to the wells and incubated. Following washing, a horseradish peroxidase (HRP) labelled anti-Human IgG conjugate is added to the wells, which binds to the immobilized Herpes simplex virus Type 1 and 2-specific antibodies. TMB is then catalyzed by the HRP to produce a blue color product that changes to yellow after adding an acidic stop solution. The density of yellow coloration is directly proportional to the amount of Herpes simplex virus Type 1 and 2 IgG sample captured in plate.

  • Tested applicationsSuitable for: Indirect ELISAmore details
  • PlatformMicroplate

Properties

    Applications

    Our Abpromise guarantee covers the use of ab108741 in the following tested applications.

    The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

    Application Abreviews Notes
    Indirect ELISA Use at an assay dependent concentration.

    Protocols

    References for Human Anti-Herpes simplex virus Type 1 and 2 IgG ELISA Kit (HSV1+2) (ab108741)

    ab108741 has not yet been referenced specifically in any publications.

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