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[小麦籽粒过氧化物酶WP1基因的原核表达、纯化及多克隆抗体制备]

[Prokaryotic expression, purification and preparation of polyclonal antibody for wheat grain peroxidase WP1 gene].

作者信息

Shan Liwei, Tang Ruchun, Liu Sanyang, Fan Sanhong, Guo Aiguang

机构信息

College of Life Sciences, Northwest A & F University, Yangling 712100, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2011 Jan;27(1):26-30.

Abstract

Wheat peroxidases 1 (WP1) is the major cationic peroxidase of wheat (Triticum aestivum) grain, which is involved in the development of seeds and an important factor to affect the final processing quality of flour. We constructed a prokaryotic expression vector pET28a-WP1, and transformed it into E. coli host strain T7 Expression. His-tag fused WP1 existed as inclusion body, and the recombinant protein was purified by Ni-NTA resin affinity chromatography under denatured condition. The purity of target protein reached 98%. The recombinant WP1 was refolded by gradient urea dialysis, then used as antigen to immune rabbit to prepare polyclonal antibody. The result of ELISA showed that the titer of rabbit anti-WP1 antiserum was higher than 1:625 000. The result of Western blotting demonstrated that the prepared WP1 polyclonal antibody could be used to detect WP1 with high specificity.

摘要

小麦过氧化物酶1(WP1)是小麦(普通小麦)籽粒中的主要阳离子过氧化物酶,它参与种子发育,是影响面粉最终加工品质的重要因素。我们构建了原核表达载体pET28a-WP1,并将其转化到大肠杆菌宿主菌株T7 Expression中。His标签融合的WP1以包涵体形式存在,重组蛋白在变性条件下通过Ni-NTA树脂亲和层析进行纯化。目标蛋白的纯度达到98%。重组WP1通过梯度尿素透析进行复性,然后用作抗原免疫兔子以制备多克隆抗体。ELISA结果显示,兔抗WP1抗血清的效价高于1:625 000。Western blotting结果表明,所制备的WP1多克隆抗体可用于高特异性检测WP1。

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