Selected article for: "ABV testing and dot blot elisa"

Author: Escandon, Paulina; Heatley, J Jill; Berghman, Luc R; Tizard, Ian; Musser, Jeffrey MB
Title: Comparison Of Four Anti-Avian IgY Secondary Antibodies Used In Western Blot And Dot-Blot ELISA To Detect Avian Bornavirus Antibodies In Four Different Bird Species
  • Document date: 2019_11_12
  • ID: 2sr6ds4r_31
    Snippet: Western blot and immunofluorescence assays are considered gold standards in serologic testing for ABV. N-protein is the immunodominant antigen, 9,27 thus a recombinant N-protein was utilized as the antigen of interest in our assays. The use of the Western blot in our study was two-fold: 1) to verify the seropositive/seronegative status of the plasma samples and 2) to evaluate the use of the different secondary antibodies as compared to the dot-bl.....
    Document: Western blot and immunofluorescence assays are considered gold standards in serologic testing for ABV. N-protein is the immunodominant antigen, 9,27 thus a recombinant N-protein was utilized as the antigen of interest in our assays. The use of the Western blot in our study was two-fold: 1) to verify the seropositive/seronegative status of the plasma samples and 2) to evaluate the use of the different secondary antibodies as compared to the dot-blot ELISA. Anti-macaw and anti-bird IgY secondary antibodies produced strong reactions at 38-41 kDa, but additional bands were seen at 17, 27, and 30 kDa. These bands likely represent degraded N-protein to which the secondary antibodies were able to bind.

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