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Pecan (Carya illinoinensis) detection using a monoclonal antibody-based direct sandwich enzyme-linked immunosorbent assay

机译:山核桃(Carya Inlinoinensis)使用单克隆抗体的直接夹心酶联免疫吸附测定检测

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摘要

A commercially available (BioFront Technologies) monoclonal antibody-based direct sandwich enzyme-linked immunosorbent assay (ELISA) for pecan detection was evaluated. The assay can detect 0.5 ppm of pecan and reliably quantify > 1.5 ppm of pecan with 14% intra- and inter-assay variabilities. The detection antibody did not exhibit cross-reactivity with 155 foods/ingredients tested at 100,000 ppm, although it registered 0.6% and 0.8% cross-reactivity with 10,000 ppm of English walnut and black walnut, respectively. The target antigen was stable against autoclaving, blanching, frying, microwaving, and roasting. The antigen was detected in a variety of food matrices with 80.5-111.6% and 22.2-154.5% recoveries for pecan-spiked and incurred samples, respectively. The assay did not yield any false negative results among tested commercial and in-house prepared samples, however, it recognized two commercial products with declared walnut and no declared pecan as positive. In conclusion, the ELISA was sensitive and robust for pecan detection and quantification and was specific other than the low level of cross-reactivity with walnut species.
机译:评价可商购(BioFront Technologies)单克隆抗体的直接夹心酶联免疫吸附测定(ELISA)用于磷脂检测。测定可以检测0.5ppm的悬浮蛋白,可靠地定量> 1.5ppm的悬浮蛋白。 14%内和测定间可变性。检测抗体没有以100,000ppm测试的155种食品/成分表现出交叉反应性,尽管它分别注册了与10,000ppm的英国核桃和黑核桃的交叉反应性0.6%和0.8%。靶抗原稳定对抗高压灭菌,烫伤,油炸,微波和焙烧。抗原在各种食物基质中检测到80.5-111.6%和22.2-154.5%,分别用于悬浮的磷酸盐和引发的样品的回收率。该测定没有在经过测试的商业和内部准备样品中产生任何假阴性结果,然而,它公认了两种商业产品,宣布核桃,尚未宣布普通为正面。总之,ELISA对山核桃检测和定量敏感和稳健,并且除了与核桃物种的低级别交叉反应性的特异性。

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