摘要
应用基因工程技术,将抗人Clq轻链可变区基因(ClqV_L)由重组质粒pGEM-ClqV_L中分离,克隆进表达载体pJLA502。该表达载体含CITs857抑制子基因,通过开温诱导法,重组表达子在宿主菌HB101中表达,获得抗人Clq轻链可变区片段,SDS-PAGE表明其分子量范围为12~13KD。这为进一步抗人Clq小抗体的表达积累了经验,有利于用于抗原-抗体结构功能的研究。
The light chain variable gene of mouse anti-human Clq monoclonal antibody was isolated fromrecombinant plasmid pGEM-Clq,subsequently cloned into expression plasmid pJLA502 with CITs857 gene,and transformed into E. coli strain HB101.Shifting the culture temperature from 30℃ to 42℃ led to the ex-pression of ClqV_L with a molecular weight of 12~13KD. The result is significant for the furthe constructionof anti-Clq Fv,as well as for the study of structure-function between Clq and anti-Clq antibody.
出处
《免疫学杂志》
CAS
CSCD
北大核心
1995年第3期147-149,165,共4页
Immunological Journal
基金
国家自然科学基金