This kit is comprised by HRP conjugate, other reagents and ELISA Microtiter plate pre-coated with recombinant Classical Swine Fever Virus (CSFV) E2 antigen. Apply the principle of enzyme-linked immunoassay (ELISA) to detect CSFV-Ab in serum, plasma of porcine. During the experiment, add control and samples into the ELISA Microtiter plate, CSFV-Ab will be bound with the antigen on the ELISA Microtiter plate. Then wash the plate to remove unbound components, horseradish peroxidase (HRP) conjugate is added to each ELISA Microtiter plate well. The unbound HRP Conjugate will be removed by washing and substrate reagent is added for color development. At last, end the reaction by adding Stop Solution to produce a yellow product. There is a positive correlation between the OD value of samples and the concentration of CSFV-Ab. Measure the absorbance value of each well by using a microplate reader with 450 nm (630 nm) wavelength, then we can judge whether CSFV antibody exist in the sample.
