对6A95Z20型喷油泵RFD型调速器调速特性曲线的探讨

本文为解决解放C△141K_2型柴油载货汽车,在使用中出现的发功机减速迟缓问题,通过理论分析和对比试验研究,找到了故障原因。提出了对生产厂家给定的调速特性曲线进行修正方案,解决了使用维修中急待解决的实际疑难问题。提高了车辆的利用率,延长了精密偶件的使用寿命,降低了维修费用,取得了明显的经济和社会效益。     

抗绵羊进行性肺炎病毒单克隆抗体杂交瘤细胞株的建立

用提纯的OPPV细胞抗原免疫BALB/c小鼠脾脏与SP2/0小鼠骨髓细胞融合,融合率为70%,以ELISA双抗体夹心法进行检测,阳性率为20%,经过有限稀释法克隆出1A₆、2B₈、1G₃、2G₄4株分泌抗OPPV抗原的单克隆体杂交瘤细胞株.选择抗体分泌滴度高的1A₆细胞进行了较详细的研究,结果表明,其核内染色体数为96～110条,抗体属性为IgG1,轻链为K链,IFA试验表明产生的McAb对OPPV有特异性,细胞传30代并在液氮中保存半年后复苏仍能稳定地分泌抗OPPV McAb,细胞分泌抗体的ELISA滴度腹水为6.4×10⁴,上清为640,McAb经硫基乙醇还原后在SDS-PAG上呈现2条区带,一条为重链部分,MW50000,另一条为轻链部分,MW为25000.     

红豆草茬地放牧结合补饲青干草对草地羔羊育肥效果的研究

1986～1987年期间在甘肃农大牧草站进行了以红豆草茬地放牧结合补饲青干草对草地羔羊育肥效果的试验。比较了在放牧基础上3种补饲处理(即单燕麦草、单红豆草和燕麦+红豆草混合干草)对两种类型羔羊(即甘肃高山细毛羊和边甘杂种一代羔羊)增重和肉用性能的影响。试验结果表明,7月龄边甘杂种羔羊或9月龄甘高羔羊的期末活重均已超过35公斤,胴体重超过17公斤,屠宰率为47％～49％。     

昆明鼠卵母细胞的去核及其去核率的观察

本文研究昆明鼠卵母细胞的去核方法，并通过对去核卵母细胞的固定染色，显示其中期Ⅱ染色体，由此观察统计其确定的去核率。     

水稻不育系粒黑粉病普遍率与严重度间的关系

 稻粒黑粉病(病原菌Neovossia horrida (TaK.)Padw. et A. Kahn)是杂交稻繁殖制种田不育系上的主要病害,流行频率高,危害损失大。普遍率和严重度的关系(I-S关系)是植病流行学观测技术上的一个重要问题。     

山东绿篱树种的种质资源及其应用

在调查山东绿篱应用现状的基础上，从了解山东绿篱树种的种质资源状况着手，针对其种类、应用方式、生长特性和适应性挖掘利用方面进行分析。认为目前在绿篱种质资源应用方面存在一些问题，针对这些问题提出了一些建议。     

履带板用高锰钢强韧化研究

本文根据履带板的失效特征和机理,提出了高锰钢的铬、钼再合金化,稀土、钛变质处理和重结晶热处理工艺综合强韧化方案.经实验证实,综合机械性能显著改善.     

‘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.