C_R704玉米与S_C704玉米过氧化物酶同工酶及生理指标分析

C_R704玉米与S_C704玉米各时期的过氧化物酶同功酶谱无明显差别,二者遗传基础一致,但酶活性C_R704玉米高于S_C704玉米。经测定三系杂种C_R704玉米在叶绿素、糖、淀粉及蛋白质含量均优于单交种S_C704玉米。     

The Location Algorithm of QRS Waves Based on Fractal Box Dimensions Detection Methods

We research fractal characteristics of ECG signal, and find that it is logarithmic linear relationship between the boxes number covering signal and box scale. It is shown that ECG signal have some characteristics. Further more, we discover that fractal dimensions at QRS site are higher than others when using a time windows to detect signal. Based on this foundation, we raise a location algorithm of QRS waves which is based on fractal boxes dimension detection methods. The application results of this algorithm show that it can get rid of noise in ECG effectively with high speed, so this algorithm can be used in real time detection of ECG signal.     

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.     

生沛素对皖系粗毛兔生产性能的影响

选择42日龄皖系粗毛兔幼兔42只,根据体重、性别,随机分成3组,分别饲喂含1‰、2‰生沛素日粮和对照组日粮.结果表明,添加1‰、2‰生沛素组产毛量比对照组分别提高17.5%(P＜0.01)和19.1%(P＜0.01);增重提高11.2%(P＜0.05)和12.5%(P＜0.05);每只兔一次产毛的经济效益比对照组分别提高2.96元和1.13元.另外,添加生沛素的试验组兔毛品质也比对照组有所提高和改善.     

实验猴志贺氏菌检出、血清分型及药物敏感性试验

采用实验动物国家标准(GB/T 14926.47-2001)的检验方法,对144份待出口实验猴粪便样品检测,检出志贺氏菌2株,阳性检出率1.39%。血清学分型,均属于B群志贺氏菌,血清型分别为X变种和Y变种。药敏试验结果表明,2株分离菌对先锋V、氟哌酸和环丙沙星高度敏感,而对青霉素、红霉素和复方新诺明耐药。     

高梁不育系Tx3197A减数分裂中染色体行为

以Ｔｘ３１９７Ｂ和晋粱５号为对照，对Ｔｘ３１９７Ａ进行了观察。结果发现，减数分裂前期Ⅰ和中期Ⅰ无明显异常。自后期Ⅰ开始，染色体行为出现了多类型的异常现象，导致减数分裂不能正常进行，无法形成花粉粒，从而产生雄性不育。     

配送中心线路优化方法的探讨

基于目前配送中心线路优化的各种方法,根据实际情况对上述算法进行分析和比较,并针对模拟退火法、遗传算法在配送线路优化问题中的具体应用,提出不同情形下的求解策略。     

不同包被液对ELISA检测五号病病毒抗体的比较试验

０．０５ＭｐＨ９．６碳酸盐缓冲液和０．０５ＭＰＨ１３ＮａＯＨ溶液作为包被液，分别用于间接ＥＬＩＳＡ检测乙型五号病病毒抗体。结果表明，用０．０５ＭＰＨ１３ＮａＯＨ溶泡包被可完全灭活五号病病毒抗原而用０．０５ＭＰＨ９．６碳酸盐缓冲液却有８７％的五号病病毒抗原未被杀灭；用于检测时，以０．０５ＭＰＨ１３ＮａＯＨ溶液为包被液在敏感性及检测结果的梯度方面都优于用０．０５ＭＰＨ９．６碳酸盐缓冲液。     

妊娠黄牛的血液动力流变学观察

首次应用XXG－A型心血管功能测试仪以无创伤检测技术对16例妊娠黄牛22项血液动力流变学指标做了检测，并首次对怀孕黄牛的血液动力流变学特征做了报道。     

Development of a semi-selective medium and an immunofluorescence colony-staining procedure for the detection of Clavibacter michiganensis subsp. sepedonicus in cattle manure slurry

Various compounds and basal media were tested for their suitability to create a semi-selective medium for isolation ofClavibacter michiganensis subsp.sepedonicus (Cms) from cattle manure slurry containing c. 10⁸ colony forming units (cfu) per ml.Plating efficiency of Cms in yeast glucose mineral medium (YGM) was 104% compared with yeast peptone glucose medium. Nalidixic acid, polymyxin B sulphate and the experimental disinfectant S-0208 inhibited colony growth of cattle slurry bacteria as compared with Cms in YGM. The optimal concentration of these inhibitors in combination was determined by modified agar diffusion tests and by pour plating in 24-well tissue culture plates. The semi-selective medium YGMI consisted of YGM supplemented with nalidixic acid (2 mg/l), polymyxin B sulphate (30 mg/l) and S-0208 (125 mg/l). Plating efficiency varied for Cms between 50.9 and 69.6%, for cattle slurry bacteria between 1.8 and 2.5% and for saprophytes from potato heel end extracts between 11.5 and 27.4%.Differentiation of Cms colonies from other colonies was based on their small and bluish colony morphology in pour plates and on immunofluorescence colony-staining (IFC). IFC of a pure culture of micro colonies of Cms in YGM was possible after one day incubation (colonies c. 5 cells). Green background fluorescence in the agar gels was prevented by addition of Tween 20 (0.1%) to the washing buffer and the use of 1% agar gels. IFC of macro colonies of Cms in YGMI, visible with 4x objective magnification, was possible after 4 days. The detection level of the target organism in artificially inoculated cattle slurry in YGMI based on colony morphology varied between 1.4×10³ and 2.3×10⁴ cfu per ml of cattle slurry. Miniaturized plating combined with IFC, using wells in tissue culture plates (=16 mm), proved suitable for detection, but was c. 30 times les sensitive. The recovery of Cms was negatively correlated with the number of saprophytic colonies in the agar plates (R ²=0.74).