Abstract

The research aimed at preparing, purifying and characterizing the immunoglobulin G, for dog, goat and rabbit, and the anti-IgG serum for the same species. The IgG species purification was done through precipitation, using ammonium sulfate solution and ion exchange chromatography (DEAE-cellulose). Checking the IgG purity was done by immunoelectrophoresis (IEF), for the corresponding anti-species serum, and by polyacrylamide gel electrophoresis in denaturant system (SDS-PAGE). Using IEF, we obtained a precipitation arch with cathodic migration, whereas using SDS-PAGE, we obtained a fraction with a molecular mass of 150 KDa. Dog and goat anti-IgG serum was prepared on rabbit, and the rabbit anti-IgG serum on goat, by IgG hyperimmunisation concealed in Freund adjuvant at a 1 to 1 ratio. Sensitivity and specificity testing of antisera was performed by immunoenzymatic test (ELISA). There were highlighted the high titers of antibodies to the dilution of 1:500 for anti-IgG rabbit and goat sera, and 1:400 for anti-IgG dog serum. Specificity testing of dog and rabbit anti-IgG in the heterologous system showed results which are in the negative range. The DO values were high for goat anti-IgG serum, sheep IgG serum and sheep anti-IgG serum and goat anti-IgG serum, due to antigenic kinship between these species. The reagents prepared will be used in great specificity and sensitivity immunodiagnostic tests.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call