Abstract
ABSTRACTAn approach for production of specific polyclonal antiserum against TSWV using recombinant TSWV nucleocapsid protein as antigen was described. The ability to detect TSWV in purified preparations and in contaminated leaf extracts was compared. The purified IgG fraction and obtained conjugate with alkaline phosphatase were suitable for routine DAS-ELISA diagnostics or TSWV.
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