加气混凝土砌块在建筑中的应用

蒸压加气混凝土是一种新型的节能、环保墙体材料 ,它在基本建设中运用具有良好的综合经济效益和社会效益。这里以加气混凝土在建筑中的应用实例 ,从材料、施工、抹灰及存在的问题等方面论述了它的运用情况 ,可供有关设计和施工人员参考。     

桃需冷量遗传特性的研究

对桃的９个杂交组合４６３株杂种实生苗需冷量进行测定,统计结果表明：桃需冷量是由多基因控制的,Ｆ＿１需冷量平均值较亲中值短,不同组合偏离程度不同,南山甜桃、红日、玛丽维拉、白凤、大久保需冷量育种值分别为１５９、２１６、３１９、８３１、８３４ｈ,遗传传递力分别为７９%、５４%、９２%、８３%、９３%。需冷量的遗传力为８９．６９%。萌芽开花与需冷量密切相关。     

液压液用聚醚研究

Polyethers is one of the main components of water-glycol-base non-inflammble hydraulic fluid. This paper describes an optimized technique synthesizing polyether from ethylene oxide and epoxypropane. The synthetic polyethers meets the technical requirement     

无源电力滤波器电路参数非线性约束优化

对偏调谐类单调谐滤波器提出了非线性的束优化模型，运用大系统理论协调优化单调谐滤波器和高通滤波器，实例计算表明，该方法是对以往单调谐滤波器设计计算方法的一大改进。     

中国美利奴羊(新疆型)无角类型培育理论依据及测交试验结果

绵羊角的有无是由或主要由一个基因位点（Locus）上的三个等位基因（H、h’、h）所决定。三个等位基因的遗传方式是：H为显性无角基因，对h为完全显性，即Hh基因型均表现无角性状；h为隐性有角基因，即hh基因型均表现有角性状；h，为一个频率很低的基因，对h为不完全显性，即h＇h基因型仍表现为有角性状；但H对h’基因为不完全显性，即Hh’基因型可能出现角痕（角突或角基）。而h’h’基因型公羊表现为小角、发育残缺不全的矫型角，母羊表现为无角。培育无角革的关键是选择使用无角公羊，通过测交试验能确定无角公羊基因的纯合度，从而决定如何使用。     

继电保护用电流互感器的暂态特性数字仿真及电磁优化设计

本文在分析CT的暂态特性及其动态磁化过程的基础上,建立了计及铁芯饱和、局部磁滞回环、动态剩磁影响的CT单、复励磁暂态过程数字仿真模型,提出了继电保护用P、TPX、TPY、TPz级CT的电磁优化设计方法,编制了计算机程序,用于CT的电磁优化设计及数字仿真分析.     

湖南高品质棉研究进展与发展对策

根据国家将长江中下游棉区定位为50￣60支纱生产基地的区划要求,分析国内外及湖南棉区高品质棉的研究现状及发展前景,并针对限制湖南高品质棉发展的“瓶颈”因素提出了加强纺织技术改造,是当务之急,创造与引进优异新种质新材料、遗传品质改良工程,优异纤维品质的基因工程是根本途径,加速新品种选育是重中之重。     

‘Plantibodies’: a flexible approach to design resistance against pathogens

Engineering resistance against various diseases and pests is hampered by the lack of suitable genes. To overcome this problem we started a research program aimed at obtaining resistance by transfecting plants with genes encoding monoclonal antibodies against pathogen specific proteins. The idea is that monoclonal antibodies will inhibit the biological activity of molecules that are essential for the pathogenesis. Potato cyst nematodes are chosen as a model and it is thought that monoclonal antibodies are able to block the function of the saliva proteins of this parasite. These proteins are, among others, responsible for the induction of multinucleate transfer cells upon which the nematode feeds. It is well documented that the ability of antibodies to bind molecules is sufficient to inactivate the function of an antigen and in view of the potential of animals to synthesize antibodies to almost any molecular structure, this strategy should be feasible for a wide range of diseases and pests.Antibodies have several desirable features with regard to protein engineering. The antibody (IgG) is a Y-shaped molecule, in which the domains forming the tips of the arms bind to antigen and those forming the stem are responsible for triggering effector functions (Fc fragments) that eliminate the antigen from the animal. Domains carrying the antigen-binding loops (Fv and Fab fragments) can be used separately from the Fc fragments without loss of affinity. The antigen-binding domains can also be endowed with new properties by fusing them to toxins or enzymes. Antibody engineering is also facilitated by the Polymerase Chain Reaction (PCR). A systematic comparison of the nucleotide sequence of more than 100 antibodies revealed that not only the 3′-ends, but also the 5′-ends of the antibody genes are relatively conserved. We were able to design a small set of primers with restriction sites for forced cloning, which allowed the amplification of genes encoding antibodies specific for the saliva proteins ofGlobodera rostochiensis. Complete heavy and light chain genes as well as single chain Fv fragments (scFv), in which the variable parts of the light (V_L) and heavy chain (V_H) are linked by a peptide, will be transferred to potato plants. A major challenge will be to establish a correct expression of the antibody genes with regard to three dimensional folding, assembly and intracellular location.