WANG Ya-nan, WANG Xiao-fei, DING Han, ZHANG Hai-tang, FAN Guo-ying, WANG Zi-liang. Preparation of monoclonal antibody against trivalent chromic ion and development of colloidal gold immunochromatographic assay for detecting total chromium content in food[J]. Science and Technology of Food Industry, 2016, (18): 63-69. DOI: 10.13386/j.issn1002-0306.2016.18.004
Citation: WANG Ya-nan, WANG Xiao-fei, DING Han, ZHANG Hai-tang, FAN Guo-ying, WANG Zi-liang. Preparation of monoclonal antibody against trivalent chromic ion and development of colloidal gold immunochromatographic assay for detecting total chromium content in food[J]. Science and Technology of Food Industry, 2016, (18): 63-69. DOI: 10.13386/j.issn1002-0306.2016.18.004

Preparation of monoclonal antibody against trivalent chromic ion and development of colloidal gold immunochromatographic assay for detecting total chromium content in food

  • Object: To prepare monoclonal antibody against Cr3+chelate EDTA complex( Cr3+- EDTA m Ab) and develop colloidal gold immunochromatographic assay for detecting total chromium content in food( Cr- Strip).Method: The isothiocyanate method was employed to synthesize Cr3+- i EDTA- BSA,which was identified by UV and ICP- AES.The hybridoma lines that secrete Cr3+- EDTA m Ab were established by cell fusion and Cr3+- EDTA m Ab were induced from in vivo method and their immunological properties were analyzed. Based on Cr3+- EDTA m Ab,Cr- Strip was developed and its traits were verified.Results: Three hybridoma lines were screened out and the best one was 2A11G5. The Kaof Cr3+- EDTA m Ab was 2.69 × 109 L / mol and its IC50 against Cr3+- EDTA was9.84 μg / L and it had little or no cross- reactivity with other metal ion. The Cr- Strip could be accomplished qualitative detection of Cr3+- EDTA in 10 minutes,and its detection limit was 5 μg / L,its coincidence rate was 100%compared with ICP- AES. Conclusion: The high quality Cr3+- EDTA m Ab had been generated and the Cr- Strip which was more sensitive had been developed successfully.
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