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Locomotor activity was measured with amonitor and rCMRglc were measured with the quantitative autoradiographic[14C]2-deoxyglucose procedure in 62 brain regions of Fischer-344rats at 2, 30, 60, 120, and 180 min after IV administrationof saline or midazolam 5 mg/kg.

在静脉注射盐水或咪达唑仑(5 mg/kg )后2,30,60,120和180min 后测定 T-344大鼠62个脑区的自主运动活性及 rCMRglc (用2 -去氧葡萄糖(14C )放射性定量测定法)。

The quantitative autoradiographic 2-(14C)-deoxy-D- glucose methods were used to assess the local cerebral glucose utilization in 46 brain structures in rats suffering from heatstroke.

利用2-(14C)-去氧葡萄糖自动放射显影定量法,分析了大白鼠热中风后脑部46个神经核的葡萄糖代谢率。

Rotavirus-infected and 12 healthy children were studied in this work. Real-time PCR was used to evaluate the population levels of Bacteroides spp.

实时定量PCR结果表明,轮状病毒感染个体肠道内拟杆菌的16S rRNA基因拷贝数与健康个体相比平均下降了2个数量级,具有显著性差异(P.05)。

To collect the feces of patients and the control group then a quantitative analysis on Enterobacteriacea, Enterococcus, Lactobacillus, Bifidobacterium Bacteroides and Yeast was made.

采用光冈法对糖尿病患者、服用拜糖平患者及正常人群粪便中的双歧杆菌、肠杆菌、肠球菌、酵母菌进行定性、定量检测。

There are two methods to detect and quantitative analysis Neu5Ac, one is high performance liquid chromatography with the use of Aminex87H column, the other one is barbituric acid method.

对Neu5Ac的检测和定量也有两种方法,一种是利用Aminex87H酸性糖基柱,通过高效液相色谱测定;另一种是硫代巴比妥酸法测定。

The method is easy, fast and precise and can fit for determining barrenwort in the health food .

该法简便、快速、定量准确、精密度好,适合于保健食品中淫羊藿苷的测定。

Mg/ml, the average recovery 101.6%, and the RSD lower than 10%. Conclusion:The method is easy, fast and precise and can fit for determining barrenwort in the health food .

该法简便、快速、定量准确、精密度好,适合于保健食品中淫羊藿苷的测定。

The expression of LbMT2 gene in L. bicolor in response to CuSO4, CdCl2, NaCl, cold, and PEG was further investigated using real time quantitative PCR.

利用实时定量PCR方法研究了二色补血草在CuSO4、CdCl2、NaCl、低温和PEG胁迫下不同时间该基因的表达模式。

Objective To quantify the burden of Borrelia burgdorferi in different representative tissues from the murine host by real time quantitative PCR.

目的 用实时荧光定量PCR确定伯氏疏螺旋体感染小鼠模型不同组织的病原体载量。

Methods : We subjected C57BL/6J mice to CS (whole body exposure, 90 min/day) for various periods, and used laser capture microdissection to isolate bronchiolar epithelial cells for analysis of mRNA by quantitative reverse transcription-polymerase chain reaction.

研究方法:研究者将 C57BL/6J 小鼠分别在不同时间周期暴露于CS(全身暴露,90分钟/天),用激光捕获显微切割技术分离细支气管上皮细胞,然后用定量逆转录多聚酶链反应分析上皮细胞的mRNA。

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