(2+1)维CD方程的精确行波解

考虑(2+1)维CD方程,利用行波变换和截断展开法,并结合含参数Riccati方程解的技巧,获得了(2+1)维CD方程的许多新的精确行波解.     

手性配合物[Mn（csal-R,R-chxn）]Cl的CD光谱和不对称催化作用

以5-氯-水杨醛双缩（1R,2R）-环己二胺（CSA-DMC）为原料制备了手性[Mn（csal-R,R-chxn）]Cl配合物,测定了手性配体CSA-DMC的荧光光谱,研究了手性配合物[Mn（csal-R,R-chxn）]Cl的CD光谱及催化苯乙烯不对称环氧化反应的催化性能.结果表明：手性配体CSA-DMC的荧光发射峰处于517 nm;利用激子裂分方法和d-d跃迁关联法推测了手性席夫碱配合物[Mn（csal-R,R-chxn）]Cl绝对构型为（R）Δλ构型;最适宜反应条件下,催化苯乙烯的不对称环氧化反应的转化率为74.9%,催化剂选择性为67.6%,对映体过量百分率（e.e.）为12.3%     

Efficacy of anti-CD20 chimeric Fab’ fragment on proliferation of B lymphoma cells

The variable domain of heavy chain (V_H) and light chain (V_L) genes of anti-CD20 monoclonal antibody HI⁴⁷ were cloned from anti-CD20 ScFv expression vector pCANBTEcd20 by PCR and ligated into vector pYZF to construct chimeric anti-CD20 Fab’ fragment expression vector pYZFcd20. Chimeric anti-CD20 Fab’ fragment was expressed inE. coli 16C9 and purified by protein G affinity chromatography. Competitive inhibition assay showed that anti-CD20 Fab’ fragment inhibited binding of HI⁴⁷ to CD20 on the surface of Daudi cells. Results from MTT assay indicated that chimeric anti-CD20 Fab’ fragment inhibited the proliferation of Daudi cells, IC₅₀ = 69 μg/mL. Affinity of chimeric anti-CD20 Fab’ fragment was determined, K_a was about 8.9×10⁸ (mol/L)⁻¹.     

Isolation, purification and characterization of secondary structure of antifreeze protein fromAmmopiptanthus mongolicus

Antifreeze protein (AFP) from Ammopiptanthus mongolicus leaves was isolated and purified with DEAE cellulose 52, Sephacryl 300, heat treatment and preparative isotachophoresis. The molecular weight of AFP was 50 ku by SDS-PAGE measurement. The average thermal hysteresis activity (THA) of AFP was 0.35℃ at 5 mg/mL using a differential scanning calorimeter (DSC). This AFP showed heated stability. From circular dichroism (CD) of AFP spectral data from 195—240 nm, a well-defined secondary structure of 11% a-helix, 34% antiparallel b-sheet and 55% random coil for the plant AFP was deduced.     

Construction and expression of retroviruses encoding dual drug resistance genes in human umbilical cord blood CD34+ cells

A series of retro viral vectors encoding humanmdr1 gene alone as wetl as in combination with either humanmgmt gene or human mutantSer ³¹-dhfr gene are engineered. The resultant retroviruses are used to transduce human umbilical cord blood CD34⁺ cetls. It has been shown that expression of dual drug resistance genes in transduced cetls confers a broad range of resistance to both kinds of corresponding drugs. These data suggest a rationale for the use of such double chemoresistance gene constructs in anin vivo model in which transduced hematopoietic cetls will acquire multiple protection against the cytotoxic side effects of combination chemotherapy and may have future application in chemoprotection of normal tissues, thus killing tumor cetls more effectivety.     

基于光盘质量的动态自适应技术的设计与实现

采用动态自适应技术来根据光盘质量对主轴转速作自适应的调整,以最佳的速度读取光盘数据,有利于数据的顺利读取和保护光头组件。相应地针对光盘反射信号的质量提出一种间接评估数据质量的方法,设计了基于光盘质量的动态自适应技术,并应用于高速光盘驱动器伺服控制系统中。     

α-胰凝乳蛋白酶在不同介质中稳定性的研究

测定了α-胰凝乳蛋白酶在不同介质中的活性及稳定性。研究了有机溶剂性质、pH值、离子强度及离子类型对α-胰凝乳蛋白酶活性与稳定性的影响,并通过CD谱初步研究了α-胰凝乳蛋白酶在不同pH值缓冲液中的二级结构变化。研究结果表明,α-胰凝乳蛋白酶在某些有机溶剂中能在较长时间内维持较高的酶活性。α-胰凝乳蛋白酶在3种pH值不同的缓冲液中的CD谱表明其在pH＝10.0的稀溶液中的α-螺旋和（或）β-折叠含量较高。在不同pH值条件下,离子强度对α-胰凝乳蛋白酶的活性与稳定性的影响不同。     

浅谈随书附盘的特点及其管理与利用

分析了目前出现的各种随书附盘的特点,归纳出对随书附盘进行管理的几种模式,探讨了如何更好地利用随书附盘的途径。     

试析体育院校图书馆图书附件光盘的管理和使用

介绍了图书附件光盘的内容和作用,分析了体育院校光盘收藏和使用现状、管理服务模式,并提出了提高图书附件光盘利用率的方法和建议。     

基于开源架构的随书光盘管理及发布系统设计

对随书光盘检索及下载系统的架构、功能模块和数据库的设计以及采用的主要技术进行了说明。