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Then press the PAGE DOWN key, and watch from trackside cams as the car zooms around the track.

然后按&PAGE DOWN&键，在赛车围绕赛道行驶时从赛道边的摄象机来观察这一切。

The recombinant pET-Lip vector was transformed into E.coliBL21 and induced to express by 1mmol/L IPTG at 37℃. An expected 80kDa fusion proteinwas expressed. SDS-PAGE analysis showed the fusion protein located in the supernatant ofbacteria lysate by sonication. The fusion protein was purified by HisTrap~ HP Kit and coulddegrade tributyrin.

该菌株经IPTG诱导可表达分子量约80 kDa的融合蛋白，SDS-PAGE分析表明融合蛋白位于菌体超声裂解后的上清中，用蛋白纯化试剂盒HisTrap~ HP纯化后得到单一的目的蛋白，约80 kDa，且纯化的融合蛋白具有脂酶活性，可以分解三丁酸甘油酯。

One integrative transformant was obtained through PCR and phenotype identification, designated as A.oryzae ONL1. The 7-day fermentation broth of A.oryzae ONL1 could hydrolyze tributyrin verified by forming transparent cleared zone on tributyrin plate, and the enzyme activity reached 2.5 U/mL. The SDS-PAGE electrophoretic map of the fermentation broth demonstrated that there was a typical RML band at 32.5 kDa.

其培养7天的培养液上清在以三丁酸甘油酯为底物的平板上形成清晰的水解透明圈，碱滴定法酶活测定表明培养液酶活可达2.5 U/mL，培养液上清的SDS-PAGE图谱在32.5 kDa处有RML的特征条带。

Through SDS-PAGE and Western blot analysis, it was indicated that the expressed products were specifically detected by positive serum of mouse against Trichinella.

SDS-PAGE电泳显示表达蛋白为36ku的融合蛋白，将表达产物进行Western blot检测，可以被小鼠旋毛虫的阳性血清识别。

Chicken IL-15(ChIL-15), Which was discovered in 2001, plays a main role in activating NK cells and CD8+ memory T cells, and may therefore have potential as a vaccine adjuvant.According to published ChIL-15 gene sequence, a pair of primers were designed and synthesized to clone ChIL-15 cDNA from ConA-activated chicken splenocytes by RT-PCR. Recombinant plasmid pUC19ChIL-15 carrying the ChIL-15 gene was constructed. The gene encoding mature ChIL-15 (mChIL-15) was amplified from pUC19ChIL-15 by PCR and cloned into pMD 18-T vector. After digested with Kpn I /Pst I , the mChIL-15 gene was subcloned into prokaryotic expression vector pPRoEX橦Ta and transformed into E.coli DH5a .The transformant was induced by IPTG, and the recombinant ChIL-15(rChIL-15) was expressed as a fusion protein with a histidine hexamer tag at the N-terminal end of the protein. Following expression, the protein was purified by ProBond?Nickel-Chelating Resin. The uninduced and induced protein lysates and the purified protein were separated by SDS-PAGE and transferred onto nitrocellulose membrane to identify rChIL-15 by Western blot. The rChIL-15 was used to immune the guinea pig to obtain rChIL-15 polyclonal antibody.

参考已发表的ChIL-15基因序列，设计合成引物，应用RT-PCR技术从刀豆球蛋白A活化的白来航鸡脾淋巴细胞中克隆ChIL-15 cDNA，将其与SmalⅠ酶切处理的pUC19载体连接，构建重组质粒pUC19ChIL-15；用PCR技术从pUC19ChIL-15中扩增出去信号肽的成熟ChIL-15(mChIL-15)基因，与pMD 18-T载体相连构建重组质粒pMDChIL-15；然后用KpnⅠ／PstⅠ双酶切下mChIL-15基因片段，定向亚克隆到经同样酶切处理的带有6个组氨酸标签的表达载体pP_RoEX~HTa中，构建重组质粒pP_RoChIL-15，对其测序确认读框正确后，转入大肠杆菌DH5α中诱导表达并进行纯化，用重组ChIL-15(rChIL-15)免疫豚鼠，制备多克隆抗体；再用HindⅢ／PstⅠ从质粒pP_RoChIL-15上切下mChIL-15基因，定向亚克隆到经同样酶切处理的杆状病毒转移载体pMelBacB中，经酶切、PCR和序列测定鉴定后，与杆状病毒线形化DNABac-N-Blue~(TM DNA共转染Sf9昆虫细胞，经三轮蚀斑纯化，构建重组杆状病毒rBac-ChIL-15，用该重组病毒感染处于对数生长期的Sf9细胞，按不同的时间收取样品，离心后对其上清和沉淀进行SDS-PAGE和Western blot分析。

As a result of the analysis of unreduced SDS-PAGE, the content of large molecular rCPB polymers was decreased inβ-ME solutions as well.

经非还原SDS-PAGE分析，添加β-巯基乙醇后，溶解rCPB聚体的含量减少。

Methods The recombinant plasmid of CPB, pET-21a-CPB, was constructed and transformed into E. coli BL21(DE3). The expression was induced in 25℃and 37℃, respectively. The obtained inclusion bodies were dissolved in different denaturing solution systems. The protein concentration was determined in order to indicate the solubility of CPB inclusion bodies in the denaturing solution. And probable mechanism for the solubility differences was illuminated by the analysis of unreduced SDS-PAGE.

方法构建CPB重组质粒pET-21a-CPB，将其导入表达菌株BL21（DE3）中，分别在25 ℃和37℃进行诱导表达；所得包涵体分别用不同浓度尿素添加不同还原剂溶解，以溶液中的蛋白质浓度判定其溶解性，利用非还原SDS-PAGE分析其溶解性提高的原因。

Yolk protens of Bombyx mandarina are also composed of vitellin, egg specific proteins and 30K proteins on the base of SDS-PAGE of egg subsracts of Bombyx mori and Bombyx mandarina.

通过家蚕与野桑蚕卵的内容物的SDS-PAGE，分析了野桑蚕卵黄蛋白主要有卵黄磷蛋白，卵雌异性蛋白和30K蛋白组成。

Using different dosages of He-Ne laser irradiated the developmental eggs of Antheraea yamamai. Compared with control plot, their hatchabilities were increased and their larval duration was influenced. Individual such as abnormal and premature mutants was also obtained. The blood protein and esterase isoenzyme of their pupa were analyzed with PAGE, found some changes in band r umber and activity. All those indicated that He-Ne laser has some inductive effects on physiological and biochemical characters of Antheraeayamamai.

不同剂量的He-Ne激光辐照天蚕发育卵，当代与对照相比较，孵化率提高、幼虫龄期经过缩短，产生附属肢畸变、早熟等变异体；对蛹血蛋白质、酯酶同工酶进行PAGE分析，其谱带数和活性也产生了变化，显示He-Ne激光对天蚕的生理生化性状具有诱变效应。

The high molecular weight glutenin subunit composition of 49 wheat varieties were fractionated by SDS-PAGE. The results showed that the frequency of subunits 5+10 was 64% in 39 Chinese wheat varieties.

利用SDS-PAGE电泳分析了49个国内外小麦品种的高分子量谷蛋白亚基组成，结果表明：39个国内小麦品种中，5+10亚基的频率达64%。

I will endeavour to find you some assistance.

我尽力帮你找人帮忙。

At first I only know bruck is the idol of American younglings, afterwards I returned back to Taiwan ,even in Beijing last year ,I saw her poster everywhere, I was so surprised at her charm.

起初我只晓得布鲁克雷德丝是美国少男少女崇拜的偶像，后来回台湾，甚至去年在北京，居然也四处看见她的海报，才惊讶她的魅力之大。