Construction, expression, purification and polyclonal antibody preparation of Fas extracellular region gene
- VernacularTitle:Fas胞外区基因的构建、表达、纯化及多克隆抗体的制备
- Author:
Jiakai ZHANG
;
Qingyu MENG
;
Xiaofeng CHENG
;
Ruizhen LIU
;
Guohong ZHUANG
- Publication Type:Journal Article
- Keywords:
Fas;
apoptosis;
polyclonal antibody
- From:
Chinese Journal of Biochemical Pharmaceutics
2010;31(1):35-39
- CountryChina
- Language:Chinese
-
Abstract:
Purpose To construct expression vector of Fas extracellular region gene(eFas) ,to express and purify recombination protein and to prepare polyclonal antibody, which have laid a foundation of studying its function. Methods The eFas gene encoding sequence was acquired through overlapping PCR, and pET-22b ( + )/eFas expression vector was constructed. Then this vector was transformed into E. coli Rosetta-gami. Re-combinant protein was expression being induced by IPTG,and was purified using Ni-NTA matrix of affinity chromatograph. The purity of recombination protein was identified by SDS-PAGE. Hereafter, the purified eFas recombinant protein was immunized to New Zealand white rabbit in order to prepare polyclonal antibody. The titer of polyclonal antibody was determined by ELISA. Results The encoding sequence and expression vector of eFas was obtained while the interest protein was mainly expressed in the inclusion body. The eFas fusion protein's expression quantity accounts for more than 30% proportion of total E. coli protein. The eFas protein we obtained was provided with the purity of at least 95 % . Conclusion The successful constrution, expression and purification of FasL fusion protein and preparation of polyclonal antibody will provide some material for further studies of Fas.
