摘要
从T载体上得到的目的基因和dhfr共扩增基因真核表达载体构建了pCI-PrP102。纯化后的重组质粒通过脂质体转染CHO/dhfr-细胞,经MTX加压筛选获得稳定表达的细胞株,间接免疫荧光试验检测到目的蛋白的表达。
:The target genes from T - vector were connected with dhfr co - amplified gene of eukaryotic vector and constructed pCI -PrP102. Purified recombinant plasmids were transferred into CHO/dhfr- cell through liposome, and obtained the stable expression of the cell strains after MTX screening, and indirect immunity fluorescence analysis detected the expression of the goal protein.
出处
《江西农业学报》
CAS
2009年第4期101-103,共3页
Acta Agriculturae Jiangxi
基金
国家自然科学基金项目(30671563)