2010
DOI: 10.1016/j.aca.2010.09.042
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Hapten synthesis, monoclonal antibody generation, and development of competitive immunoassays for the analysis of picoxystrobin in beer

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Cited by 51 publications
(43 citation statements)
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“…Carboxyl functionalized haptens were activated using N,N'-disuccinimidyl carbonate, and the corresponding NHS ester was purified by flash chromatography following a previously published procedure (Esteve-Turrillas et al, 2010). Briefly, the hapten (0.1 mmol) and N,N 0 -disuccinimidyl carbonate (33.3 mg, 0.13 mmol, 1.3 equiv.)…”
Section: Hapten Synthesis and Activationmentioning
confidence: 99%
“…Carboxyl functionalized haptens were activated using N,N'-disuccinimidyl carbonate, and the corresponding NHS ester was purified by flash chromatography following a previously published procedure (Esteve-Turrillas et al, 2010). Briefly, the hapten (0.1 mmol) and N,N 0 -disuccinimidyl carbonate (33.3 mg, 0.13 mmol, 1.3 equiv.)…”
Section: Hapten Synthesis and Activationmentioning
confidence: 99%
“…Haptens were covalently coupled to proteins by the active ester method as previously described for other molecules (Esteve-Turrillas et al 2010). Carboxylated haptens were activated by reaction with DSC and EtN3 under smooth conditions, and the corresponding active esters were purified by silica gel chromatography and characterized by 1 H NMR spectroscopy.…”
Section: Immunoreagent Preparationmentioning
confidence: 99%
“…Mp 172-175°C (from cold methanol); IR v max /cm À1 (KBr) 3500-2500, 3435, 3305, 3035, 2928, 2853, 1691, 1653, 1513, 1473, 1444, 1388, 757; 1 (8) To activate hapten BLa5 (7) for protein conjugation, the N-succinimidyl ester was prepared ( Fig. 1) according to a previously described procedure (Esteve-Turrillas et al, 2010). Briefly, acid 7 (30 mg, 0.068 mmol) and N,N 0 -disuccinimidyl carbonate (DSC) (27.9 mg, 0.109 mmol, 1.6 equiv.)…”
Section: Preparation Of 5-mentioning
confidence: 99%