To identify the function of cloned ATL-cDNA, the recombinant expression vector was constructed, and the Pichia pastoris GS115 was used as a host for expressing ATL gene.
为了验证所克隆到的ATL-cDNA序列的功能,构建重组表达载体,以毕赤酵母GS115为宿主进行功能表达分析。
参考来源 - Aspergillus tamarii FS132脂肪酶基因的克隆及其在毕赤酵母中的表达·2,447,543篇论文数据,部分数据来源于NoteExpress
应用推荐