FOOD SCIENCE ›› 0, Vol. ›› Issue (): 284-287.

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Development of Indirect ELISA Kit for Detecting Phorate Residue

  

  • Received:2010-04-16 Revised:2011-01-04 Online:2011-02-25 Published:2011-01-20

Abstract: An indirect enzyme-linked immunosorbent assay(ELISA)kit was developed to monitor phorate residue. The optimal concentration of coating antigen was 4 mg/L and the optimal dilution ratio of antibody was 8000. The cross-reaction ratio was less than 20%. The regression equation of inhibition rate for phorate was y = 18.846x+6.9949 with a linear detection range of 1-5000μg/L. Results indicated that the detection limit was 4.90μg/L and IC50 was 191.37μg/L. The recovery rates were higher than 75%. The intra-assay and inter-assay coefficients were less than 10%. The developed kit can be stored at 4℃ or-20 ℃ for 270 days.

Key words: phorate, residue, enzyme-linked immunosorbent assay(ELISA), kit