[丝裂铁蛋白2/SLC25A28的原核表达及兔多克隆抗体制备]。

Lei Liu, Yating Nie, Lan Ding, Yu Gu, Yuan Yuan, Jing Ye
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引用次数: 0

摘要

目的构建人丝裂铁蛋白2 (SLC25A28)原核表达质粒,并对其进行表达纯化,制备兔多克隆抗体。方法构建原核表达质粒pET28a(+)-SLC25A28-His,转染大肠杆菌BL21 (DE3),用异丙基-β- d -硫代半乳糖苷(IPTG)诱导表达。SLC25A28蛋白以包涵体形式提取,溶解于8 mol/L尿素中,经His-NTA柱纯化。通过免疫家兔制备抗slc25a28多克隆抗体,并通过Western blot检测其特异性。结果构建了pET28a(+)-SLC25A28-His, SLC25A28蛋白在大肠杆菌BL21 (DE3)中成功表达,纯度达90%。Western blot结果表明,抗SLC25A28多克隆抗体能够特异性识别睾丸中SLC25A28蛋白。结论成功地在大肠杆菌中表达了人SLC25A28,并制备了兔SLC25A28特异性多克隆抗体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Prokaryotic expression of mitoferrin 2/SLC25A28 and rabbit polyclonal antibody preparation].

Objective To construct the prokaryotic expression plasmid of human mitoferrin 2 (SLC25A28), and to express and purify the protein for preparing its rabbit polyclonal antibody. Methods The prokaryotic expression plasmid pET28a(+)-SLC25A28-His was constructed and transferred into E. coli BL21 (DE3), and induced with Isopropyl-β-D-thiogalactopyranoside (IPTG). The SLC25A28 protein was extracted in form of inclusion bodies, and was further purified by His-NTA column after dissolved in 8 mol/L urea. The anti-SLC25A28 polyclonal antibody was prepared by immunizing rabbits, and its specificity was determined by Western blot analysis. Results pET28a(+)-SLC25A28-His was constructed and SLC25A28 protein was successfully expressed in E. coli BL21 (DE3) with the purity up to 90%. The Western blot results indicated that anti-SLC25A28 polyclonal antibody was capable to recognize specifically the SLC25A28 protein in testis. Conclusion The human SLC25A28 is successfully expressed in E. Coli, and the rabbit polyclonal antibody specific to SLC25A28 is prepared.

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