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inclusion body相关的网络例句

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与 inclusion body 相关的网络例句 [注:此内容来源于网络,仅供参考]

It was to study the purification, renaturation and activity of recombinant Methionine γ-Lyase expressed as inclusion body in E.

探索以包涵体形式表达的重组蛋氨酸裂解酶的纯化、复性方法,并对其活性进行检测。

How to refold inclusion body proteins with many pairs of disulfide bonds into natural conformation with high efficiency is a challengeable problem at present, and it is becoming one of the industrial bottlenecks in bioengineering field.

如何对富含二硫键的包涵体蛋白进行高效的体外复性使其获得正确的空间结构是重组蛋白生产所面临的巨大挑战,现已成为制约生物工程技术产业化的瓶颈问题之一。

The reservoir time are decided by inclusion body homogeneity temperature and terrestrial heat history, the time is the telophase of the Cretaceous period, the reservoir time and tectonic movement is accordant.

利用烃类流体包裹体均一温度并结合盆地东部的地热史,厘定出石千峰组气藏成藏时间为晚白垩世,这与盆地整体向西倾斜、地层大量剥蚀的时间基本上是一致的。

But when they expressed alone, cry26 gene leaded inclusion body formation within or outside of the exosporium, whereas cry28 gene only induced crystal formation outside of exosporium. All of the proteins could not stably exist.

而当两个cry基因单独存在时,cry26基因表达合成的内含体位置不确定,大部分在芽胞外壁外侧形成,少数在芽胞外壁内侧形成;而cry28基因则只在芽胞外壁外侧表达合成内含体。

The N gene ORF was then subcloned into pET-30a vector and the recombinant plasmid was transformed into E.coli BL21 (DE3) and induced with IPTG. The protein expression was determined by SDS-PAGE. The expressed protein had a molecular weight of 54.4 Ku that existed as inclusion body. Thin-layer scanning showed that the expression product accounted for 30.5% of the total bacterial proteins. The recombinant protein possessed native biological activity and could react with anti-PEDV hyperimmune serum in Western blot.

以阳性质粒为模板,用分别含有BamH Ⅰ和Xho Ⅰ酶切位点的上、下游引物扩增得到ORF,其PCR产物经BamH Ⅰ和Xho Ⅰ双酶切后定向克隆到pET-30a载体,构建的重组质粒命名为pET-30a-PN;将pET-30a-PN转化到大肠杆菌BL21 (DF3)中,在IPTG诱导下进行表达;SDS-PAGE结果表明表达出与预期大小相符的约54.4 Ku的重组蛋白,重组蛋白以包涵体形式存在;薄层扫描结果表明表达产物占菌体总蛋白的30.5%;Western blot分析表明表达的重组蛋白能与抗PEDV高免血清反应,说明该重组蛋白具有免疫学活性。

Results We obtained a lysogenic bacteriophage MZTP01with clear plaque and 1 mm diameter. Fragment D with 2362bp (Genebank No. AY639599) was obtained after the phage DNA hydrolyzed by HindⅢ/EcoRⅠ. Among fragment D, the pep gene with molecular weight of 47 kDa and length of 1101bp was cloned and expressed. Recombinant M15 (pQE30pep) was built and overexpressed in Escherichia coli with a 47kDa clear band. At the same place a clear band was observed by Western blot. Judging from the time course expression, we could conclude that PEP protein produced at 1 hour after induction and then increased gradually. PEP protein was mainly in the form of inclusion body in the recombinant and slowed the growth speed of host. Homologous comparison of PEP protein from phage MZTP01 with other PEPs from BLAST were that phage MZTP01 PEP protein had 100% homologe with that of Escherichia coli K12, and most of others took the similarity in the range between 37%~84%.

诱导获得的溶原性噬菌体MZTP01斑点清晰,直径约1mm,成斑时间12h;从噬菌体基因组DNA双酶切(HindⅢ/EcoRⅠ)片段中回收长度为2362bp的D片段(Genbank登录号: AY639599),又从D片段中克隆了长度为1101bp、编码367aa、分子量为47kDa的pep基因,表达载体M15(pQE30pep)在大肠杆菌(Escherichia coli, E.coli)中表达获得了47kDa的清晰表达带,在1h 时开始产生蛋白并有逐步上升的趋势; Western blot 也在47kDa处得到一条清晰的条带;可溶性分析表明PEP蛋白在重组菌株中是以不可溶的包含体形式存在的,该蛋白的产生明显地抑制了宿主的生长速度;噬菌体PEP氨基酸序列之间的同源性比较表明,噬菌体MZTP01 PEP蛋白与来自E.coli K12噬菌体的PEP蛋白的同源性程度最大。

The most of the product became soluble from inclusion body by lowering induction temperature. At the same time the gene was cloned into vector pMAL-p2X, which was translated in E. coli TB1 and expressed a fusion protein. We optimized the induction time and achieved high expression. But there was no obvious product secreted in the periplasm extract. Almost all fusion protein is expressed soluble in cytoplasm.

利用融合型表达载体pTYB11-EFE融合型表达,对诱导剂IPTG的浓度和诱导温度进行了优化,通过降低诱导温度使产物由包含体变成可溶性融合型产物;利用融合型分泌表达载体pMAL-p2X构建了表达载体pMAL-p2X-EFE-7~#,对诱导时间进行了优化,获得了较高的表达量,但发现产物没有明显的分泌表达,绝大部分是以可溶形式存在于胞内。

The research aimed to observe the inclusion body in pyramidale cytoplasm in hippocampus of cerebral cortex in shepherd dog with rabies.

观察患狂犬病的牧羊犬大脑皮层海马的锥体细胞浆内的包涵体。

But 5-helix was apt to form inclusion body when expressed directly in prokaryotic cell and was difficult to renature, which causes inconvenience to future study.

但5-helix基因在原核细胞中直接表达时易形成包涵体,复性困难,给研究带来不便。

A 1: Uninduced supernant of cell lysate by sonication; 2: Induced supernant of cell lysate by sonication; 3: Uninduced precipitate of cell lysate by sonication; 4: Induced inclusion body of cell lysate by sonication; 5: Purified ULBP4 protein; M: Low molecular marker proteins.

2.3 体外NKG2D结合实验和细胞因子分泌实验间接ELISA检测结果显示:原核表达复性后的ULBP4能与人NKG2D结合,而带His标签的无关蛋白则不能与之结合,说明复性后的ULBP4仍能维持正确的天然构像。

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