它们改变了这个酶切割淀粉样蛋白前体的方式。
研究目的:克隆表达人肠激酶轻链编码基因,以期应用于融合蛋白的切割与纯化。
Objective: To clone and express the gene of human enterokinase light chain which would be used in the cleavage and purification of fusion proteins.
利用最佳体系对融合蛋白进行切割,经过活性检测发现,目的肽没有抑菌活性。
We used the best system to cut on the fusion protein, after activity detected the purpose of peptide has no antibacterial activity.
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