This review a few methods for the rapid detection of E . coli .

本文综述了几种 大肠杆菌 的快速检测法.

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E . moving any additional information that is relevant into the new db.

大肠杆菌 移动任何附加信息到新的数据库相关.

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Process control of recombinant Escherichia fed - batch culture should be optimized.

优化重组大肠杆菌 高密度 发酵的调控工艺.

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BL 21 and an expected 14×103 fusion protein was isolated by SDS - PAGE.

重组原核表达质粒 pET28a -COP转化大肠杆菌BL21后,经IPTG诱导表达,获得一条约14×103的融合蛋白.

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Producing the hydrogen fuel uses the harmless bacteria Escherichia coli.

利用无害的大肠杆菌,生成氢气燃料.

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But the structure and function of HPI in thesestrains is unclear.

但HPI在致泻性大肠杆菌中的结构、功能仍不清楚.

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The resonance scattering spectra of colibacillus have been studied.

研究了大肠杆菌的共振散射光谱.

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Objective: Express major epitope domain of NS 1 of PPV in E.

目的: 用大肠杆菌表达猪细小病毒NS1基因的主要抗原表位区.

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The Separating Identification and Test of Drug Sensitivity to E.

与大肠杆菌的分离鉴定及药敏试验>>相似的文献.

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This paper summarized the advance about heterologous gene high expression in E.

作者综述了有关外源基因在大肠杆菌中高效表达的研究进展.

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Objective To clone and express Trp operon gene of E.

目的克隆并表达大肠杆菌色氨酸操纵子基因,提高其酶活性.

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Purpose Molecular cloning and expression of pro nattokinase gene with E.

目的构建纳豆激酶原基因克隆,实现其在大肠杆菌中的表达.

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CONCLUSION: Expressed Fab fragment has the antigenic specificity for human erythrocytes.

结论: 于大肠杆菌表达了具有抗原结合特性的人抗-D抗体Fab段抗体分子.

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Methods: The recombinant fusion protein MBP hEra was expressed in the E.

方法在大肠杆菌中,表达重组MBP?hEra融合蛋白.

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The sqHAS gene was ligated into expression vector pSE 380 under trc promoter.

构建表达质粒pSE-sqHAS并转化大肠杆菌DH5α,诱导培养后在细胞膜中检测到sqHAS蛋白及活性.

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