浅谈CFG桩复合地基

CFG桩是一种新的加固地基方法。具有适用范围广、加固地基效果明显、综合利用粉煤灰和工业废渣等优点。经济效益和社会效益好,极有推广价值。     

PCR技术检测猪伪狂犬病毒及其潜伏感染部位的研究

本研究合成了伪狂犬毒糖蛋白ｇｐ５０基因引笺，该引物能够扩增糖蛋白ｇｐ５０基因中４３４－６５１之间的２１７ｂｐＤＮＡ片段，该片段含 ＳａｌＩ酶切位点，应用引物对几种不同的伪狂犬病毒株多聚酶链式反应扩增结果全为阳性。     

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.     

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。     

VSV的RT-PCR快速检测方法的建立

选取水泡性口炎病毒 N基因序列 ,设计 1对引物 ,建立检测水泡性口炎病毒的 RT- PCR方法。对VSV各毒株进行检测 ,结果均为阳性 ,而对反刍动物病毒性疾病相关病毒进行检测 ,结果均为阴性。结果表明所建立的 RT- PCR技术可用于水泡性口炎的诊断和流行病学调查     

鸡新城疫病毒B_(95)株的RT-PCR检测方法研究

本试验设计了一对B95 株的特异引物NDV -P1/P2,探讨了对其进行RT-PCR检测的可行性。结果证明 ,用该引物可以扩增出一条310bp的特异核酸带 ,敏感性为0.0043ng/ul。     

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).