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1.Compared with the Mut~+, the Mut~s-hFL transformants showed higher expression level with less coloring contamination in the product and easier purification for hFL.
与Mut~+型相比,Mut~s转化子在含营养和色素较少的BMM培养基中即有高表达,且表达产物杂蛋白少,易于纯化。收藏指正
2.Mut-HPI was less easily digested by trypsin and CPB than Met-HPI.
Mut-HPI与改造前的Met-HPI相比,不易被胰酶和羧肽酶B(CPB)降解。收藏指正
3.Two mutants,named mut-1 and mut-2,with decreased ADH activity were screened out by yeast peptone dextrose(YPD)agar medium containing allyl alcohol. These two mutants had decreased ADH activities of 41.63% and 50.29% compared with the parent strain.
在含丙烯醇的YPD筛选培养基上筛选获得两株ADH活力降低的突变株mut-1和mut-2,检测突变株mut-1和mut-2的最大ADH活力分别为35.67和43.09U/mL,是原始菌株的41.63%和50.29%。收藏指正
4.SDS-PAGE results indicated that there was a clear target band in Muts and Mut+ recombinant Culture supernatant after 48 hours culture respectively.
实验结果表明,诱导表达48h后,Mut+和MutS重组子表达的产物在SDS-PAGE胶上都出现了清晰的目的带。收藏指正
5.Mut für die Zukunft: Analyse der Rede von Bundespr?sident Horst K?hler bei der Gedenkveranstaltung zum 60. Jahrestag des Endes des Zweiten Weltkrieges in Europa.
知耻后勇,面向未来——解读德国总统克勒纪念二战结束60周年的讲话收藏指正
6.SDS-PAGE results showed that there was a clear target protein band in Mut+ recombinant supernatant after 48 hours of culturing, while a faint band only in Muts recombinant after 72 hours.
结果表明,诱导培养48小时后,Mut~+重组菌株表达产物在SDS-PAGE胶上显现出清晰的目的蛋白带,而Mut~s重组菌株培养72小时才能显示微弱的目的带;收藏指正
7.Methods Site-directed mutagenesis was conducted to obtain 2 mutant human XIII A recombinant plasmids, mut-PCI/FXIIIA. Normal wild type factor XIII A recombinant plasmid, wt-PCI/FXIIIA, and mut-PCI/FXIIIA, were transfected into cultured COS7 cells line, renal fibroid cell of African green monkey using Superfect reagent respectively, The expression levels of DNA, RNA and protein of human factor XIII, both wild type and mutant, were detected by PCR, RT-PCR and Western blotting.
方法 构建正常人FXIIIA重组表达质粒 (wt PCI/FXIIIA) ,通过定点突变获得上述 2种突变的FXIIIA重组表达质粒 (mut PCI/FXIIIA) ,并分别将它们转染到COS7细胞表达 ,PCR、RT PCR和Western印迹检测转染细胞中人FXIIIA的DNA水平、RNA水平及其蛋白质的表达量。收藏指正
8.2、 Construction of luciferase reporter plasmid containing human a-SMA genepromote (p895-Luc) and mutant Smad2 plasmid (pSmad2~(mut)): The human a-SMAgene promoter (-895~+9bp) was cloned by PCR from human genomic DNA andwas inserted into vector pGa(?) 3-basic at MluI-XhoI site and form p895-Luc.
2、构建含人α-SMA基因启动子序列的荧光素酶报告基因质粒(p895-Luc)和Smad2突变表达质粒(pSmad2~(mut)):以人基因组DNA为模板用PCR扩增人α-SMA基因启动子-895~+9bp序列,插入到pGal3-basic质粒的MluⅠ和XhoⅠ酶切位点之间形成p895-Luc。收藏指正
9.An increase of intracellular DNR retention in si-MDR1-treated cells was observed, confirming the inhibition of P-gp function by siRNA targeted MDR1. One base pare mutated control (si-MDR1-Mut) lost the effect of si-MDR1 on both the degradation of mdr1 mRNA and the reduction of P-gp expression.
2.小干扰RNA对白血病MDR细胞系K562/A02 mdr-1转录、P-gp表达、P-gp功能及K562/A02细胞耐药表型的影响,并进行RNAi的特异性分析。 设计与si-MDR1仅有一个碱基突变的序列(si-MDR1-mut)为对照。收藏指正
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