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By exchanging the carboxyl termini of NR2A and NR2B subunit, surface NR2B-containing NMDA receptors occurred more in a clustering manner,whereas NR2A-containing ones more diffusedly.

然而，NR2亚单位中与这些支架蛋白相结合的功能区却无法直接解释NR2A与PSD-95蛋白之间的这种特异性的相互作用。

Being stimulated with LPS 1μg·ml-1, RAW 264.7 cells were observed under LASER confocal microscopy. Erythrine P65 subunit of NF-κB aggregated at nuceluses, which made Erythrine fluorescence of nuceluses much stronger than that of endochylema.

LPS 1μg·ml-1干预RAW264.7细胞后，激光共聚焦显微镜下观察结果显示，红染的NF-κB P65亚基聚集于细胞核，使胞核红色荧光明显强于胞浆。

The 648 bp mitochondrial cytochrome c oxidase subunit I gene was examined in 8 species of raptors (5 species in Accipitridae, Falconiformes; 3 species in Strigidae, Strigiformes) by PCR with universal primers. 99 additional barcode sequences were downloaded to explore whether the DNA barcodes could distinguish between these species.

用DNA条形码通用引物扩增了我国8种猛禽（14只个体）的线粒体细胞色素c氧化酶亚基I基因，选取648 bp DNA条形码标准区域，结合99条猛禽条形码序列，探讨DNA条形码对猛禽的识别和鉴定。

The amino acid sequence of the N-terminal portion of the StdA, the major fimbrial subunit of Std fimbriae, reveals no homology to that of the non-Salmonella strains and is conserved within Salmonella strains.

Std线毛的主要线毛次单位为StdA，而其N端的胺基酸序列仅与沙门氏菌属有同源性，在其他非沙门氏菌属中则无同源性。

To investigate the relationship of subunit of F18 fimbrial adhesin with the adhesion effect,adhesive inhibition tests were performed using antibodies specific for the subunits FedA,FedE and FedF.

利用抗大肠埃希氏菌F18菌毛主要结构亚单位FedA特异抗体和次要结构亚单位FedE、FedF特异抗体，研究了F18菌毛与小肠上皮细胞的黏附特性。

The adhesion test showed that small intestinal epithelium cells of 30-35-day-old postweaning piglets with both genotype M307~ and M307~ could adhere to the standard E.coli strain express F18ab fimbriae, the recombinant E.coli express F18ac rE.coli1534 and the recombinant pnirBMisL-fedF E.coli displaying FedF subunit on the surface of E.coli, but small intestinal epithelium cells with genotype M307~ and 3-day-old piglet could not adhere to the three kinds of bacteria descried above, the latter with good adherence capability of 987P fimbrial E.coli.

9仔猪小肠上皮细胞的黏附试验结果显示，30～35日龄M307~基因型和M307~基因型断奶仔猪的小肠上皮细胞均能与表达F18ab菌毛标准菌株107／86、诱导表达F18ac菌毛的重组大肠杆菌rE.coli1534及诱导菌体表面展示表达F18黏附亚单位FedF的重组大肠杆菌pnirBMisL-fedF发生黏附作用，而同日龄M307~基因型断奶仔猪的小肠上皮细胞均不能与上述三株大肠杆菌发生黏附作用。3日龄易感仔猪小肠上皮细胞也不能黏附上述三株大肠杆菌，但可以很好地黏附表达于987P菌毛的大肠杆菌。

It was also found that it was basic subunit B3 of 11S glycinin that mainly degraded during the germination period and there was almost no degradation effect on 7S and 11S, main components in soybean storage protein.

大豆发芽过程中，内源蛋白酶主要使11S大豆球蛋白的碱性亚基B3发生降解，对贮藏蛋白的主要成分7S和11S几乎没有作用。

Based on DNA sequence and the molecular mass of E.coR I and Pst Ifragments,the physical map of the gene encoding the A1aB1b-subunit of glycinin wasconstructed.

根据E.coR I、Pst I酶切片段及DNA序列分析结果，构建了大豆球蛋白A1aB1b亚基基因的物理图谱。

The result indicates the length of the clone sequence is 963bp and shares a similarity of 45.24 % with the published Glycine max glycinin subunit G7 (Gy7) gene promoter.but have more similar to quantity and distance of promoter elements, they all contained typical TATA-box, CAAT-box and necessary regulatory motifs of seed-specific expression.

测序结果表明所克隆的片段长为963bp，与预期设计的大小一致，该片段与已发表的11S球蛋白基因启动子序列的相似性为45.2％，但所含的启动子序列元件的数量和距离上很相似，均具有有典型的TATA盒和CAAT盒，以及种子特异表达所必须的调控元件。

These shoots were examined by PCR,PCR-Southem hybridization and DNA dot blotting.Results indicated that the geneencoding A1aB1b subunit of glycinin has been actually introduced into mulberry.

用PCR、PCR-Southem及DNA斑点杂交等方法对这些Km抗性苗进行了鉴定，结果证实大豆球蛋白基因确已被导入桑树体内。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。