摘要
Rb基因cDNA844bp片段,与高效原核表达载体pBV221重组,构建了重组表达质粒pRB844,在大肠杆菌中成功地表达了Rb基因的产物,其分子量约32kD,表达量约占菌体总蛋白的10%-15%,初步纯化其纯度可达50%-60%,进一步纯化其纯度可达98%以上。经家兔免疫后,获得了抗Rb基因产物的抗体,这为Rb基因的进一步深入研究提供了条件。
b cDNA 844bp fragment was inserted into the expression vector pBV221. The recombinant plasmid pRB844 highly expressed a 32kD protein in E.coli BL21. The percentage is 10%-15% of total bacterial protein. Primary purity of the expressed protein through ureapurification is 50%-60%,the puriry could reach more than 98% through further purification.Polyclonal rabbit serum against the Rb protein is also prepared.
出处
《病毒学报》
CAS
CSCD
北大核心
1994年第1期19-23,共5页
Chinese Journal of Virology
关键词
抗癌基因
原核表达
免疫血清
Retinoblastoma susceptibility gene,Immune serum,Expression