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1.Simulations show that, compared with AODV (ad hoc on-demand distance vector) and DSR (dynamic source routing), this protocol saves the overhead of the protocol and reduces the end-to-end delay of the packet.
仿真结果表明:与AODV(ad hoc on-demand distance vector)和DSR(dynamic source routing)等协议相比,该协议节省了协议开销,减小了分组的端端时延.收藏指正
2.In this paper we use P2P technology to organize end-entities and use bloom filter vector to present CRL.
论文提出利用P2P技术组织端实体,并利用bloomfilter压缩向量代表安全凭证回收链CRL。收藏指正
3.To this end, the expression vector of Cre-ERt under the control of the mouse albumin gene promoter/enhancer, alb-Cre-ERt, was constructed, and transfected into engineering BRL (Rat hepatocytes) and BRK (Rat kidney) reporter cells which carries a chromosomally integrated ‘floxed’ βgeo gene, which is inserted between the promoter and the human alkaline phosphatase( hAP) reporter gene, thereby preventing hAP reporter gene transcription, respectively.
此 ,首先构建了在小鼠白蛋白基因调控区调控下的Cre ERt表达载体 (Alb Cre ERt) ,然后将其构件分别转染工程化的BRL(大鼠肝细胞 )和BRK(大鼠肾细胞 )细胞株 ,这些细胞携带的floxed βgeo框架位于启动子与人碱性磷酸酶基因 (hAP)之间 ,因而阻碍hAP表达。收藏指正
4.To improve the targeting of adenovirus vector for gene therapy,a fusion gene sCAR-EGF,in which epidermal growth factor gene was fused to the 3′ end of extracellular Coxsackie virus-adenovirus receptor gene,was constructed and cloned into shuttle plasmid pDC315 to obtain a recombinant plasmid pDC315-sCAR-EGF.
了提高腺病毒载体用于基因治疗的靶向性,采用PCR和体外连接的方法构建了柯萨奇病毒-腺病毒受体(Coxsackievirus-AdenovirusReceptor)胞外段sCAR和表皮生长因子(Epidermalgrowthfactor)EGF融合基因,然后将此融合基因插入穿梭质粒pDC315。收藏指正
5.The plant expression vector pBI121. 2 was digested with BamH I and Sma I , the bovine casein B gene cDNA code fragment was seperated from pBα slC184 plasmid with Bgl Ⅱ and EcoR I, the cloning process includes two steps: the first, the Bgl Ⅱ sticky end of casein B gene was ligased to BamH Ⅲ sticky end of pBI 121. 2;
牛酪蛋白全长cDNA克隆pB_aS_1C184经Bgl Ⅰ和EcoR Ⅰ双酶切,回收其中的酪蛋白基因编码片段,与经BamH Ⅰ、SmaⅠ双酶切的植物表达载体pBI121.2分两步连接:第一步载体的BamHⅠ末端与酪蛋白基因的BglⅠ粘性末端连接;收藏指正
6.③Digesting pLXSN-mB7-1 by enzyme XhoI and BamHI to gain the opened plasmid pLXSN-mB7-1 with ambly end and BamHI sticking end; Inserting IRES-mB7-2 gene fragment into it to gain the double expressing vector pLXSN-mB7-1-IRES-mB7-2;
3XhoI酶切质粒pLXSN-mB7-1,末端钝化,然后BamHI再酶切,形成含钝末端和BamHI粘末端的开环pLXSN-mB7-1质粒,将IRES-mB7-2基因片段插入其中,得pLXSN-mB7-1-IRES-mB7-2双表达载体;收藏指正
7.②Digesting vector MINV-IRES-mB7-2 by enzyme MuntI and BamHI to obtain IRES-mB7-2 gene fragment with ambly end and BamHI sticking end.
2MunI酶切载体MINV-IRES-mB7-2,末端钝化,然后BamHI再酶切,得含钝末端和BamHI粘末端的IRES-mB7-2基因片段;收藏指正
8.In simulation example contrast, the powered end velocity and wing is considered to obey normal distributing, the result indicates that the circular error probable(CEP) is reduced 11%. The feasibility of the method about lateral push vector motor firing control logic has been proved.
模型弹外弹道仿真对比时,将主动段末速度和风视符合正态分布的随机量,结果表明,火箭弹落点的圆概率误差(CEP)减小了11%,说明文中提出的脉冲点火控制算法是可行的。收藏指正
9.This paper derives the effective synthetic aperture length equation expressed as the initial position, the velocity and the synthetic aperture time when the radar operates in spotlight mode and the vehicle does uniform straight line motion, gives the ideal azimuth resolution equation expressed as the radar wavelength, the angles between velocity vector and line of sight from the antenna phase center to target at the begining and end time of synthetic aperture.
推导了雷达载体作匀速直线运动时,以载体初始位置、速度以及合成孔径时间表示的聚束照射SAR等效合成孔径长度的解析式; 给出了以雷达工作波长、合成孔径起始及止时刻速度矢量与天线相位中心目标瞄准线之间夹角表示的聚束照射SAR方位分辨率的理论表达式。收藏指正
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