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Immunology Immunoglobulins Heavy Chain IgG

Anti-Coxiella burnetii Phase 2 IgG ELISA Kit (Q-Fever) (ab178639)

Price and availability

365 193 ₸

Availability

Order now and get it on Thursday February 25, 2021

Anti-Coxiella burnetii Phase 2 IgG ELISA Kit (Q-Fever) (ab178639)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Sensitivity: 90 %
  • Sample type: Cit plasma, Hep Plasma, Serum
  • Detection method: Colorimetric
  • Assay type: Indirect
  • Reacts with: Human

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Overview

  • Product name

    Anti-Coxiella burnetii Phase 2 IgG ELISA Kit (Q-Fever)
    See all Coxiella burnetii IgG kits
  • Detection method

    Colorimetric
  • Precision

    Intra-assay
    Sample n Mean SD CV%
    Greyzone 15 3.4%
    Pos serum 16 2.6%
    Inter-assay
    Sample n Mean SD CV%
    Greyzone 5 10.1NTU/ml 10.8%
    Pos serum 16 19.5NTU/ml 1.7%
  • Sample type

    Serum, Hep Plasma, Cit plasma
  • Assay type

    Indirect
  • Sensitivity

    > 90 %
  • Assay duration

    Multiple steps standard assay
  • Species reactivity

    Reacts with: Human
  • Product overview

    Abcam’s anti-Coxiella burnetii (Q-Fever) Phase 2 IgG Human in vitro ELISA (Enzyme-Linked Immunosorbent Assay) kit is designed for the accurate qualitative measurement of IgG class antibodies against Coxiella burnetii in Human serum. 


    A 96-well plate has been precoated with Coxiella burnetii 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 Coxiella burnetii antigens. TMB is then catalyzed by the HRP to produce a blue color product that changes to yellow after adding an acidic stop solution. The intensity of yellow coloration is directly proportional to the amount of Coxiella burnetii IgG sample captured in plate.

  • Platform

    Microplate

Properties

  • Storage instructions

    Store at +4°C. Please refer to protocols.
  • Components Identifier 1 x 96 tests
    20X Washing Solution White cap 1 x 50ml
    Cover Foil 1 unit
    Coxiella burnetii Anti-IgG HRP Conjugate 1 x 20ml
    Coxiella burnetii IgG Cut-off Control 1 x 3ml
    Coxiella burnetii IgG Negative Control 1 x 2ml
    Coxiella burnetii IgG Positive Control 1 x 2ml
    Coxiella burnetii Phase 2 (IgG) Coated Microplate (12 x 8 wells) 1 unit
    IgG Sample Diluent 1 x 100ml
    Stop Solution red cap 1 x 15ml
    Strip holder 1 unit
    TMB Substrate Solution Yellow cap 1 x 15ml
  • Research areas

    • Immunology
    • Immunoglobulins
    • Heavy Chain
    • IgG
    • Microbiology
    • Organism
    • Bacteria
    • Gram negative Bacteria
    • Coxiella
    • Kits/ Lysates/ Other
    • Kits
    • ELISA Kits
    • ELISA Kits
    • Pathogen specific immunoglobulins ELISA kits
    • Kits/ Lysates/ Other
    • Kits
    • ELISA Kits
    • ELISA Kits
    • Infectious disease ELISA kits
  • Relevance

    Coxiella burnetii is an obligate intracellular bacterial pathogen, and is the causative agent of Q fever. The genus Coxiella is morphologically similar to Rickettsia, but with a variety of genetic and physiological differences. C. burnetii is a small Gram-negative bacterium that is highly resistant to environmental stresses such as high temperature, osmotic pressure, and ultraviolet light. These characteristics are attributed to a small cell variant (SCV) form of the organism that is part of a biphasic developmental cycle, including a more metabolically and replicatively active large cell variant (LCV) form. It can survive standard disinfectants, and is resistant to many other environmental changes like those presented in the phagolysosome.

Images

  • Serologic ELISA assay principle
    Serologic ELISA assay principle
    Specific antigens are coated on the 96-well plate, controls or test samples are added to the well and incubated. The wells are washed to remove any unbound Human anti-antigen antibodies (Ig). A horseradish peroxidase (HRP) labelled anti-Human Ig conjugate is added to the wells. TMB is then catalyzed by the HRP to produce a blue color product that changes to yellow after adding an acidic stop solution. The intensity of yellow coloration is directly proportional to the amount of Human anti-antigen Ig captured on the plate.

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
For licensing inquiries, please contact partnerships@abcam.com

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