生物技术通报 ›› 2017, Vol. 33 ›› Issue (7): 138-144.doi: 10.13560/j.cnki.biotech.bull.1985.2017-0104

• 研究报告 • 上一篇    下一篇

家蚕GAPDH内参蛋白多克隆抗体的制备及其检测

陈莹,王远卓,杨娟娟,郭兴国,乔惠丽   

  1. 南阳师范学院农业工程学院 河南省伏牛山昆虫生物学重点实验室,南阳 473061
  • 收稿日期:2017-02-19 出版日期:2017-07-11 发布日期:2017-07-11
  • 作者简介:陈莹,女,硕士研究生,研究方向:昆虫生理生化与分子生物学;E-mail:1142605287@qq.com
  • 基金资助:
    河南省教育厅高等学校重点科研项目(17A180031)

Preparation and Detection of Polyclonal Antibody of GAPDH Protein from Bombyx mori

CHEN Ying, WANG Yuna-zhuo, YANG Juan-juan, GUO Xing-guo, QIAO Hui-li   

  1. Henan Provincial Key Laboratory od Funiu Mountain in Insect Biology,College of Agricultural Engineering,Nanyang Normal University,Nanyang 473061
  • Received:2017-02-19 Published:2017-07-11 Online:2017-07-11

摘要: 制备家蚕GAPDH内参蛋白多克隆抗体,并对该抗体进行检测。利用PCR技术从家蚕中克隆GAPDH基因,构建其原核表达载体,转化大肠杆菌,诱导表达重组蛋白并纯化。纯化后的蛋白作为抗原免疫新西兰大白兔制备GAPDH多克隆抗体。用酶联免疫吸附法和Western blot检测抗体的效价和特异性。结果显示,成功构建GAPDH/pET-28a原核表达载体,获得高纯度的GAPDH重组融合蛋白;经SDS-PAGE和抗His单抗检测,纯化后蛋白的分子量大小与预测的一致;以该蛋白为免疫抗原,采用4次免疫方式对新西兰大白兔进行免疫,获得GAPDH多克隆抗体血清。酶联免疫吸附检测结果表明,GAPDH抗体的效价为1:8 000,并能与天然家蚕蛋白特异性结合。成功制备了家蚕内参蛋白GAPDH多克隆抗体,为深入研究家蚕中不同蛋白的生理功能和作用奠定了坚实的基础。

关键词: 家蚕, 甘油醛-3-磷酸脱氢酶, 多克隆抗体

Abstract: This work is to prepare and detect the polyclonal antibody of GAPDH protein in Bombyx mori. GAPDH gene was cloned from silkworm by PCR,then prokaryotic expression vector was constructed and transformed into Escherichia coli competent cell. The recombinant protein was induced and purified. The purified protein was used as antigen to prepare the polyclonal antibody by immunizing New Zealand purebred rabbit. The titer and specificity of the polyclonal antibody was detected by enzyme-linked immune sorbent assay(ELISA)and Western blot. As results,GAPDH/pET-28a vector was constructed successfully,and recombinant GAPDH fusion protein in high purity was obtained. SDS-PAGE and anti-His monoclonal antibody detection showed that the molecular weight of the purified protein was consistent with that predicted. GAPDH polyclonal antiserum was obtained by immunized New Zealand purebred rabbit for four times using the purified protein as an antigen. The titer of GAPDH polyclonal antibody was 1:8 000 by ELISA,and the antiserum was able to bind specifically with the total protein of B mori. Conclusively,the polyclonal antibody of GAPDH is successfully prepared,which lays a solid foundation for further studying the physiological function of different proteins in B. mori.

Key words: Bombyx mori, glyceraldehyde-3-phosphate dehydrogenase, polyclonal antibody