Based on the results, a vector-host system was established for the high expression of fusion proteins.
还探索了转录终止序列对融合基因蛋白表达水平的影响，构建了高效表达融合蛋白的载体-宿主系统。
参考来源 - 霍乱毒素B亚基融合蛋白表达系统的构建Result The target gene,about 682 bp,was obtained by PCR and the cloned VP1 gene was successfully expressed in prokaryotic cells. The expressed products were fusion proteins with molecular weight 51 kD by SDS-PAGE identification.
结果通过PCR扩增获得682 bp的目的片段,所克隆的VP1基因在原核细胞中成功表达,表达产物为融合蛋白,经SDS-PAGE鉴定分子量为51 kD,Western Blot结果表明融合蛋白具有免疫原性。
参考来源 - O型口蹄疫病毒结构蛋白基因VP1的克隆与原核表达·2,447,543篇论文数据，部分数据来源于NoteExpress
Expressed fusion proteins existed in the form of inclusion body.
重组蛋白以包涵体的形式进行表达。
This invention relates to the detection of among others tumor-specific fusion proteins and protein interactions.
本发明涉及了尤其是肿瘤特异性融合蛋白和蛋白相互作用的检测。
To tackle the above problems, creating fusion proteins with novel insecticidal activities would be an effective way.
构建抗虫融合基因会是一种新的有效的方法用以解决这些问题。
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