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In vivo, nuclear Ser-P-STAT1 was found in macrophage-rich regions of advanced murine and human atheromata.

在体研究表明,在小鼠或人的脂质斑块中,核丝氨酸磷酸化的STAT1在富含巨噬细胞的区域被发现。

The 1 kb scaffold-attachment region at 5' non-transcription region of rRNA gene of silkworm Attacus ricini was cloned into eukaryotic expression vector pLu, which contained luciferase report gene and neo selecting marker.

蓖麻蚕核糖体RNA基因非转录间隔区有一长约1kb的核骨架结合区(scaffold-associated region,SAR)。

Three kinds of small molecular copper and zinc superoxide dismutase mimics were synthesized with N, N-bis (benzimidazol-2-ylmethyl) amine (N3), N, N-bis (benzimidazol-2-ylmethyl) methylamine(MN3) and N,N-bis (benzimidazol-2-ylmethyl) benzylamine(BN3) as ligands. The com-plexes were characterized by UV, IR and element analysis and the structures were proposed.

模拟铜一锌超氧化物歧化酶的活性中心,以二(2-苯并咪唑)丙烷为桥、二(2-苯并咪唑亚甲基)胺(N3)、二(2-苯并咪唑亚甲基)甲胺(MN3)及二(2-苯并咪唑亚甲基)苄胺(BN3)为配体合成了3种异双核的小分子模型化合物,并进行了紫外、红外表征及元素分析,推测了可能的结构。

The results show that the porosity of the membrane prepared by ScCO_2 induced phase separation is higher than that prepared by conventional method;the membrane structures are significantly influenced by the process parameters;compared with the conventional immersion precipitation phase inversion,ScCO_2 induced phase separation process can effectively avoid the formation of macrovoids at suitable operating conditions;during depressurization process,the great differences in the effect of depressurization time on membranes structure for various polymer materials result from that the speed of CO_2 gaseous nuclei escaping from membrane substrate can not keep the pace with the outer depressurization rate.(2) The tendency that the interaction parameters affect the binodal curve position is illustrated by changing the interaction parameters in reasonable ranges.

研究结果表明:与传统方法相比,采用ScCO_2诱导相转化法可获得更高的膜孔隙率;通过改变操作参数可对膜的结构进行调控,且操作参数对膜结构的影响与铸膜体系的自身性质也紧密相关;在适宜的操作条件下,ScCO_2诱导相转化法能有效避免采用传统的浸入沉淀相转化法制膜时易出现的大空腔结构;泄压过程中CO_2气核从聚合物膜基体中逃逸的速度能否与膜基体外部的泄压速度保持同步,是泄压时间对不同材质膜结构影响截然不同的根源所在。

5 Mononuclear and 6 binuclear schiff base manganese complexes have been prepared.

以Schiff碱为配体制备了5个单核和6个双核锰配合物。

Compound (3) and (4) are isostructural compounds containing lanthanide binuclear dimer and 1-D lanthanide helical chain.

化合物(3)包括两种基本结构单元,由配体pydc上μ3-O桥连起来的镧双核单元和1-Dn螺旋链。

Binuclear dimmer and tetrahedron of Zn and Yb〓O〓 cubane assembled by hydrogen bond structures were obtained.

上述配合物分别具有双核二聚体结构以及氢键组装的Zn四面体和Yb〓O〓立方烷结构。

When electric fusion method was used for nuclear transfer, the fusion rate (46. 0%), cleavage rate (53. 9%) and blastocyte development rate (10.9%) of adult ear fibroblasts were significantly lower than that of fetal fibroblasts (64. 5%, 70.1%, 21. 6% respectively), fetal skin cells (71. 5%, 70.8%, 22. 1% respectively) and ovary granulosa cells (88. 2%, 79. 1%, 25. 5% respectively). There was no significant difference among other donor cells in the cleavage and blastocyst development rate of resconstituted embryos.

当用电融合法进行核移植时,成体耳部成纤维细胞的融合率(46.0%),卵裂率(53.9%)和囊胚发育率(10.9%)均显著低于胎儿成纤维细胞(64.5%,70.1%和21.6%),胎儿皮肤细胞(71.5%,70.8%和22.1%),以及卵巢颗粒细胞(88.2%,79.1%和25.5%);另外三种细胞间的卵裂率,囊胚发育率无显著差异,但卵巢颗粒细胞的融合率显著高于胎儿成纤维细胞和胎儿皮肤细胞(88.2%vs 64.4%,71.5%,P<0.05)。

BACKGROUND: Embryonic stem cells develop from early blastular inner cell mass. Under proper condition, ESCs can maintain undifferentiated state in vitro, normal diploid nuclear type, and proliferative potential. In addition, ESCs possess multi-directional differentiation capacity and can differentiate into all sorts of cells of three germ layers.

背景:胚胎干细胞来源于发育早期囊胚的内细胞团,适当条件下能在体外维持未分化状态、正常二倍体核型及无限增殖能力,且具有多向分化潜能,能够发育分化成机体3个胚层的所有类型细胞。

Results In Hyacintn bletilla group fibroblastic cell hare small soma,a little spine.

结果 白及胶组成纤维细胞胞体较小,胞突少,多呈圆形,胞核较小。

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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。

There is no differences of cell proliferation vitality between labeled and unlabeled NSCs.

双标记神经干细胞的增殖、分化活力与未标记神经干细胞相比无改变。