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anion相关的网络例句

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与 anion 相关的网络例句 [注:此内容来源于网络,仅供参考]

The results show that anion recognition of NPC is spontaneous.

研究结果表明,吡咯酰胺主体分子识别卤素阴离子是一个自发过程。

Therefore, the anion gap represents a group of anions that are present but not identified.

因此阴离子间隙是指一组存在的但不能被测定的阴离子。

Therefore, the anion gap re present s a group of anions that are present but not identified.

因此阴离子间隙是指一组存在的但不能被测定的阴离子。

In this article, ion chromatography was used to analyze anion in latex .

采用离子色谱法对乳胶制品中阴离子进行分析。

The idea of synthesis of anion receptor is alsoa base of the design of receptor for neutral molecule.

同时这种阴离子受体的设计理念进一步为中性分子受体的设计提供基础。

Finally,the influence of the cation and anion of different ionic liquids on the oxidation was studyed.

进一步研究了离子液体的阴、阳离子组成对氧化结果的影响。

The electro-oxidation in anion exchange membrane system can be carried out in larger range of anolyte acid but cation exchange membrane system only for over 0.75mol/L.

发现阴离子膜电解体系可以在较大的阳极液酸度范围内进行铈的电解氧化,而阳离子膜电解体系则必须在大于0.75mol/L的酸度条件下进行。

In this study, we isolate, purify and characterize endo-β-glucanase by Ascomycete Xylaria regalis. The cellulose-containing medium is used to induce the production of the cellulose-degrading enzymes. When these enzymes are produced at maximum level, we harvest and filtrate the culture medium. The filtrate is purified by anion exchanger column and hydrophobic interaction column (phenyl-650M). The purification fold of endo-β- glucanase increases 4.3 times, the specific activity approaches 3.7 unit/mg, and the recovery is 27.6%, respectively.

为了分离且纯化此株菌产生在培养基中的endo-β-glucanase,先将此菌在cellulose液态培养基中大量培养,在此酵素达到最高峰时,利用滤纸过滤将菌丝及菌液分开,收集粗酵素液,再经过阴离子交换树脂及疏水性层析管柱(Phenyl-650M)等步骤予以纯化,所得到最终酵素纯度为 4.3倍,比活性为3.7 unit/mg,回收率为27.6%。

The endogenous cellulase from the gut of Pheretima aspergillum by homogenization was separated by DEAE anion exchanger and gel filtration chromatography, and a single band with cellulase activity was identified by SDS-PAGE and zymography.

通过对参环毛蚓肠道组织提取液进行DEAE阴离子交换及凝胶过滤层析,获得参环毛蚓单一的内摞纤维素酶的活性组分。

To study the expression, purification and bioactivity of human augmenter of liver regeneration in Pichia Pastoris, the expression plasmid pPICZαA- ALR was constructed and transformed into P. Pastoris by the method of electroporation transformation. Induced with 0.5% methanol, the 30 kD protein in the culture supernatant of recombinant P. Pastoris was confirmed to be rhALR by SDS-PAGE and Western blot. Quantitative analysis showed that the target protein was in a level of 66% of the total protein of the culture supernatant, with a yield of 40mg/L.we had performed DEAE anion exchange chromatography two times with excessive and regular adsorption quantity consecutively, and then the rhALR above 95% purity and 52% protein recovery could be obtained by G75 molecular sieve chromatography at last step. The bioactivity assay of the purified product showed that rhALR could stimulate the proliferation of HepG2, SMMC-7721 and NIH-3T3 in vitro.

为在毕赤酵母中分泌表达人肝再生增强因子,以色谱法分离纯化后进行体外活性研究,构建表达载体pPICZαA- ALR,经电穿孔转入毕赤酵母中,用0.5%甲醇诱导表达;重组酵母培养上清经SDS-PAGE电泳和western blot鉴定后表明, rhALR以分子量为30kD的二聚体为主;定量分析结果表明,重组酵母培养上清中rhALR约占总蛋白的66%,表达量约为40mg/L;经DEAE柱和G75柱纯化后,获得的rhALR纯度大于95%,得率为52%;体外生物学活性实验表明,rhALR能明显促进HepG2、SMMC-7721和NIH-3T3细胞的增殖。

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