Expression and purification of soluble fusion protein of Toxoplasma gondii GRA6 in E. coli.

摘要

Objective To high express and purify toxoplasma gondii antigen GRA6 in E. coli which can be used to develop the genetic engineering diagnostic reagents. Methods The recombinant plasmid of pGEX-GRA6 was transformed to a bacterium BL21-Codon Plus (DE3)-RP and the recombinant product was expressed under the inducement of isopropyl-beta-D-thiogalactosidase(IPTG).