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Methodology of generation and purification of anti-beta 2 glycoprotein I antibodies

机译:抗β2糖蛋白I抗体的产生和纯化方法

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In this Method Article we are showing the methodology for generation and purification of Anti-Beta 2 Glycoprotein I (β2GPI) antibodies. First β2GPI was purified from human plasma, and recognized by Western Blot and anti-β2GPI antibodies of serum from patients with antiphospholipid syndrome (APS). The C57BL/6 mice were immunized intraperitonealy with 150?μg of protein in adjuvant (β2GPI or bovine serum albumin) on days 1, 8 and 14. Then the anti-β2GPI antibodies were purified by affinity chromatography (Affi-Gel protein A sepharose) and affinity column using human β2GPI coupled to CNBr-activated Sepharose 4B. Titles of anti-β2GPI antibodies were determined by ELISA assays.?We purified β2GPI with great efficacy and that is recognized antigenically by serum from patients with SAP or an anti-β2gpi antibody.?We found that our purified antibody had 13 fold increased activity in ELISA test compared with the control and in Western Blot recognized with β2GPI (reference and purified).
机译:在本方法文章中,我们将展示用于生成和纯化抗β2糖蛋白I(β2GPI)抗体的方法。首先从人血浆中纯化出β2GPI,并通过Western Blot和抗磷脂综合症(APS)患者血清的抗β2GPI抗体进行识别。在第1、8和14天,用150μg佐剂(β2GPI或牛血清白蛋白)中的蛋白腹膜内免疫C57BL / 6小鼠,然后通过亲和色谱法(Affi-Gel蛋白A sepharose)纯化抗β2GPI抗体亲和柱,使用人β2GPI与CNBr活化的Sepharose 4B偶联。通过ELISA分析确定了抗β2GPI抗体的标题。我们纯化了β2GPI,具有很高的功效,并且被SAP或抗β2gpi抗体患者的血清抗原识别。我们发现,我们纯化的抗体的活性增加了13倍。 ELISA试验与对照比较,并在Western Blot中用β2GPI识别(参考和纯化)。

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