Porcine Reproductive and Respiratory Syndrome Virus Antibody ELISA Kit

Short Description:

This kit comprises a coated Microtiter Plate with recombinant PRRSV proteins, HRP conjugate, and other accompanying reagents. It employs the principle of enzyme-linked immunosorbent assay (ELISA) to detect antibodies against PRRSV in the porcine serum or plasma....


  • Catalogue No.: CK-E30002
  • Catalogue No.: 96T;96T*2;96T*5
  • Sample type: serum or plasma
  • Method: ELISA
  • Storage: 12 months(2-8 ℃)
  • Abbre: PRRSV Ab

Product Details

Product Tags

Introduction:

Porcine Blue Ear Disease, caused by the Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) (also known as the Porcine Blue Ear Disease Virus), is a contagious disease characterized by reproductive disorders in adult pigs, including premature birth, miscarriages, and stillbirths, as well as respiratory abnormalities in piglets. This disease acts as an immunosuppressive disorder, often leading to secondary infections from other pathogens, with a very high mortality rate.

This assay is designed to detect antibodies against PRRSV in porcine serum or plasma. It can be employed for the assessment of immunization efficacy.

Principle :

This kit comprises a coated Microtiter Plate with recombinant PRRSV proteins, HRP conjugate, and other accompanying reagents. It employs the principle of enzyme-linked immunosorbent assay (ELISA) to detect antibodies against PRRSV in the porcine serum or plasma. During the experiment, control serum and test sample are added to the plate. After incubation, if the sample contains PRRSV antibodies, they will bind to the antigens coated on the microtiter plate. Following washing steps to remove unbound components, the HRP conjugate is added, which specifically binds to the antigen-antibody complexes on the plate. After washing again to remove unbound HRP conjugate, substrate reagents are added to the wells and react with the enzyme-labeled complexes, resulting in a blue color. The intensity of the color is directly proportional to the amount of specific antibody present in the sample. The reaction is then terminated by adding a stop solution, turning the solution yellow. The absorbance of each well is measured at a wavelength of 450nm using a microtiter plate reader (microplate reader) to determine the presence of antibodies against PRRSV in the sample.


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