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Rapid Preparation of Pure Antibodies Against Classical Swine Fever Virus from Pig Serum by Immunoaffinity Chromatography

机译:通过免疫亲和性色谱法从猪血清迅速制备纯抗体免受猪血清的典型猪瘟病毒

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After Sepharose-4B polymerbeads were activated by using epichlorohydrin, purified swine fever virus as a ligand were binded with them to prepare an immobilized affinity chromatography column, which was used to prepare antibody from high immune pig serum. Equilibrated with pH 7.4, 0.02 mol/L PBS and eluated with pH 3.4, 0.2 mol/L NaAc-HAc buffer containing 0.5 mol/L NaCl, the purified protein obtained from this columne was demonstrated to have normal activity to combine with classical swine fever virus by SDS-PAGE and ELISA. The extraction efficiency of the antibody was 2.45% of total proteins. This study offers a novel, rapid and effective method for preparation of pure antibodies against classical swine fever virus from high immune pig serum.
机译:通过使用表氯醇激活Sepharose-4B聚合物,用纯化的猪热病毒作为配体与它们结合以制备固定化的亲和色谱柱,其用于制备来自高免疫猪血清的抗体。用pH 7.4,0.02mol / L PBS平衡并用pH 3.4壳,含有0.5mol / L NaCl的0.2mol / L Naac-HAC缓冲液,从而对该硒鼓获得的纯化蛋白质具有正常的活性,与古典猪瘟结合SDS-PAGE和ELISA病毒。抗体的提取效率为总蛋白质的2.45%。本研究提供了一种新的,快速有效,用于制备来自高免疫猪血清的古典猪瘟病毒的纯抗体。

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