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In order to evaluate classification status of biocontrol B-3 and its control efficacy to pepper wilt, antifungal action of biocontrol strain B-3 to Fusarium oxysporum f.sp. vasinfectum was determined using cylinder plate method, its control efficacy to pepper wilt was study by pot and field tests, and its identification was launched by means of phenotypic characteristics observation, physiological and biochemical indexes determination and the assay of 16S rDNA sequences.

为了明确生防菌株B-3对辣椒枯萎病的防效及其分类地位,采用管碟法测定了生防菌株B-3对辣椒枯萎病菌的抑制作用,考察了其对辣椒枯萎病的防效,并采用表型特征培养观察法,生理生化测定法和16S rDNA序列分析法对菌株B-3进行了鉴定。

Methods Enzyme-linked immunosorbent assay was used to measure the serum concentrations of pepsinogen Ⅰand Ⅱin patients with erosive gastritis, atrophic gastritis, bile reflex gastritis and gastric cancer.

方法应用酶联免疫吸附测定测定糜烂性胃炎、萎缩性胃炎、胆汁反流性胃炎和胃癌患者血清胃蛋白酶原亚群的含量及PGⅠ/PGⅡ比值的变化,并与正常对照比较。

The catalytic effect of ruthenium on the oxidation decolorizing reaction of chlorophosphonazo-mk by potassium periodate in phosphoric acid medium was investigated.

研究了在磷酸介质中,痕量钌催化高碘酸钾氧化偶氮氯膦mk褪色反应特性,测定了反应级数、反应速率方程和表观活化能,拟定了反应的最佳条件,建立了一个测定痕量钌的催化动力学新方法。

If you want to get exait and reliable determination value of permanganate index, it must carry on quality control and data processing.

在环境水的测定中欲得到可靠和准确的高锰酸盐指数测定值,就必须进行质量控制和数据处理。

Therefore, experimental water should be strictly required to meet the need in order to improve the precision and accuracy of permanganate index determination.

因此在高锰酸盐指数的测定分析中,一定要严格控制实验用水使其符合要求,以提高测定的准确度和精密度。

Requirement and processing method of the experimental water used in the process of Permanganate Index through analyzing the measurement result of standard sample.

简单介绍了高锰酸盐指数测定中对实验用水的要求及实验用水的处理方法,通过对七个标准样品的实验测定及讨论。

There is often difference in the determination of permanganate index between using automatic monitoring device and the national standard method.

水质自动站测定的高锰酸盐指数数据与实验室标准方法测定结果常常产生较大的偏差。

The test results showed its deviation was less than 0.0210%~0.031 7%, conforming to the State's permissible error.

测定结果表明,铝相对标准偏差小于0.020%~0.317%,测定结果符合国家标准允许偏差。

16 Of European Pharmacopeia respectively, and the abilities in removing interference of the two methods were verified using EDAC as an indicator.

结果 同一批结合疫苗原液用两种方法测定的结果不一致,应用《中国药典》方法测定的结果明显高于第5版《欧洲药典》的方法。

Methods according to the national pharmacopoeia(2000), determinate the content of moist and ash.

按照2000版《中华人民共和国药典》的方法进行药材水分及灰分测定;运用改良的反相高效液相色谱的方法,对薯蓣皂苷元进行测定

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