以蛋白A柱为材料纯化猪肉提取物抗原多克隆抗体,建立清真食品检测试剂盒

Nurhaerani, Wayan Wariata, D. Kisworo, S. Depamede
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引用次数: 0

摘要

本研究的主要目的是纯化针对猪肉提取物的多克隆抗体,作为开发清真食品诊断试剂盒的原料。用生猪肉提取物免疫兔血清,经70℃、80℃、100℃加热后获得抗体,分33%硫酸铵两段纯化,继续进行蛋白A柱亲和纯化。采用SDS-PAGE对抗体纯化结果进行分析,同时对生肉提取物和70°C、80°C和100°C加热的提取物进行抗体活性检测。本研究结果表明,与单独使用硫酸铵纯化的抗体相比,使用硫酸铵和Protein a柱亲和组合纯化的抗体的相对纯度可达97.6%。Western blot分析表明,纯化的抗体能够检测生的和加热的猪肉提取物,温度高达70°C,总蛋白质含量为20微克的肉提取物。用70℃加热的肉提取物免疫获得的抗体与用生肉提取物免疫的兔子获得的抗体具有相同的潜力,即只能检测生肉抗原和70℃加热的猪肉抗原。从本研究的结果可以得出结论,使用硫酸铵和蛋白a柱组合纯化抗体有效地产生了纯度相对较高的多克隆抗体。在未来,需要开展进一步的研究,利用猪提取物免疫动物纯化的多克隆抗体,在70°C或更高的温度下加热。本研究的主要目的是纯化针对猪肉提取物的多克隆抗体,作为开发清真食品诊断试剂盒的原料。用生猪肉提取物免疫兔血清,经70℃、80℃、100℃加热后获得抗体,分33%硫酸铵两段纯化,继续进行蛋白A柱亲和纯化。采用SDS-PAGE对抗体纯化结果进行分析,同时对生肉提取物和70°C、80°C和100°C加热的提取物进行抗体活性检测。本研究结果表明,与单独使用硫酸铵纯化的抗体相比,使用硫酸铵和Protein a柱亲和组合纯化的抗体的相对纯度可达97.6%。Western blot分析表明,纯化的抗体能够检测生的和加热的猪肉提取物。
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Purification of polyclonal antibody against pork extracts antigens using protein A column as material for developing halal food detection kit
The main objective of this study was to purify polyclonal antibodies against pork extract as raw material for developing diagnostic kits for halal food made from animal products. Antibodies were obtained from rabbit serum which was immunized with raw pork extract, and which had been heated at 70° C, 80° C and 100° C. The purification process was carried out in two stages namely using 33% ammonium sulfate and continued with Protein A column affinity. The antibody purification results were analyzed using SDS-PAGE, while the antibody activity was tested using the western blot method on raw meat extracts and on those heated at 70° C, 80° C, and 100° C. The results of this study showed that antibodies purified with a combination of ammonium sulfate and Protein A column affinity produced relative purity of antibodies up to 97.6 per cent compared to those purified using ammonium sulfate alone. Western blot analysis showed that the purified antibodies were able to detect raw as well as heated pork extracts up to 70° C at a total protein content of 20 micro grams of meat extract. Antibodies obtained from immunizations using meat extracts that have been heated at 70° C gave the same potential as antibodies from rabbits immunized using raw meat extract, i.e. can only detect antigens of raw meat and antigens of pork heated at 70° C. From the results of this study it can be concluded that purification of antibodies using a combination of ammonium sulfate and Protein A column is effective in producing polyclonal antibodies with relatively high purity levels. In the future, further research needs to be carried out on the development of immunodiagnostics using polyclonal antibodies purified from animals immunized with pork extract that has been heated at a temperature of 70° C or more.The main objective of this study was to purify polyclonal antibodies against pork extract as raw material for developing diagnostic kits for halal food made from animal products. Antibodies were obtained from rabbit serum which was immunized with raw pork extract, and which had been heated at 70° C, 80° C and 100° C. The purification process was carried out in two stages namely using 33% ammonium sulfate and continued with Protein A column affinity. The antibody purification results were analyzed using SDS-PAGE, while the antibody activity was tested using the western blot method on raw meat extracts and on those heated at 70° C, 80° C, and 100° C. The results of this study showed that antibodies purified with a combination of ammonium sulfate and Protein A column affinity produced relative purity of antibodies up to 97.6 per cent compared to those purified using ammonium sulfate alone. Western blot analysis showed that the purified antibodies were able to detect raw as well as heated pork extracts up to ...
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