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南京赛泓瑞
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文献和实验One-Step Purification of Recombinant Proteins with the 6xHis Tag and Ni-NTA Resin
The 6xHis/Ni-NTA system is a fast and versatile tool for the affinity purification of recombinant proteins and antigenic peptides. It is based on the high-affinity binding of six consecutive histidine residues (the 6xHis tag) to immobilized
培养箱中培养。 2、实验结果 图:1×10^6/孔细胞,5μg anti-mouse CD3与CD28刺激3天后细胞形成明显克隆团 CD3/CD28 Streptamer® 多聚体法 1、实验原理 使用低亲和力的抗 CD3 和抗CD28的抗体 Fab 片段(非传统全长抗体),结合上 Twin-Strep-tag 亲和标签,形成 CD3 Fab-Strep 和 CD28 Fab-Strep。再结合可溶性蛋白多聚体 Strep-Tactin®,在亲和力作用下,即可与 TCR 和 CD28 共刺激
Recombinant DNA Engineering, Or Cloning Genes In Plasmids
and thus fusion proteins. For example there might be sequence for a fluorescent protein such as GFP or a peptide tag such as HA upstream of MCS (and downstream of promoter) so that an insert in frame will lead to the generation of a fusion protein, an N-terminal
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