生物英语翻译● Genotype analysis to test for the presence of a primary genetic marker for E. coli BLR, the insertion / deletion with Tn10 [srl-recA) 306::Tn10(TcR)].● Restriction enzyme mapping confirmed the presence of the genes and
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生物英语翻译● Genotype analysis to test for the presence of a primary genetic marker for E. coli BLR, the insertion / deletion with Tn10 [srl-recA) 306::Tn10(TcR)].● Restriction enzyme mapping confirmed the presence of the genes and
生物英语翻译
● Genotype analysis to test for the presence of a primary genetic marker for E. coli BLR, the insertion / deletion with Tn10 [srl-recA) 306::Tn10(TcR)].
● Restriction enzyme mapping confirmed the presence of the genes and sequences of interest, specifically, the individual and tandem sCT-Gly gene cartridges, the prlA4 gene, the sec E gene, the lac IQ gene, the transcription termination signals, and the kanamycin resistance gene. No additional bands were visible on the gels.
● Measurement of the cell line productivity in small-scale fermentations to define expected ranges for sCT-gly concentration in the medium.
生物英语翻译● Genotype analysis to test for the presence of a primary genetic marker for E. coli BLR, the insertion / deletion with Tn10 [srl-recA) 306::Tn10(TcR)].● Restriction enzyme mapping confirmed the presence of the genes and
●基因型分析,检测共同里BLR,有Tn10的插入//删除的一个为E.最重要基因标志打记号的人的存在srl-recA306::Tn10((TcR).
●限制性内切酶测绘证实存在该基因序列的兴趣,具体而言,个人和串联小班教学-甘氨酸基因墨盒,prla4基因,证交会E基因,紫胶智商基因转录终止信号,卡那霉素耐药基因.没有额外带清晰可见凝胶.
●在下定义小规模的发酵中细胞线生产力的度量为在介质中sCT-gly集中预期范围.