酶联免疫吸附测定
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Methods:180 HCV patients and 40 healthy controls were selected for the research, and their serum BAFF levels were detected by ELISA. The level of serum HCV-RNA in HCV patients was detected through fluorescent quantitative polymerase chain reaction and analyzed along with the clinical data of HCV patients.
选取180名HCV感染者及40名健康对照,应用酶联免疫吸附法测定血清中BAFF含量,荧光定量聚合酶链反应检测HCV感染者血清中HCV-RNA的水平,并结合HCV感染者临床情况分析。
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The symptoms such as cough, sputum and stridor etc of both groups who were treated by point application for two weeks were observed. the serum levels of il 2, tnf α both of the admission of hospital and after being treated by elisa method were measured in these cases.
采用酶联免疫吸附方法测定70例慢阻肺急性发作期患者入院初及治疗后血清中的白细胞介素 2(il 2)、肿瘤坏死因子α的水平,同时测定肺功能(fev 1%pre、fev1/fvc、mvv。
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The level of il-6 was determined with elisa and that of crp with immune turbidimetry.
用酶联免疫吸附法检测il-6,用免疫比浊法测定crp。
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To explore the clinical reliability and usability of the acridinium ester-labeled CLIP and ELISA in detection of AFP to establish a specific, effective, simple and reliable detecting method in our lab.
[目的]探讨吖啶酯标记的化学发光免疫测定(chemiluminescence immunoassay, CLIA)分析技术与酶联免疫吸附试验一步法两种方法检测甲胎蛋白(Alpha-fetoprotein, AFP)的临床可靠性、适用性。建立本室特异、有效、方便、可靠的试验方法。
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It has been reported that F185K and C280S mutations of HIV1 integrase would improve the enzyme solubility, and the catalytical activity of the enzyme was the same as that of the wildtype enzyme in vitro.
coli中进行整合酶基因表达,SDSPAGE鉴定表达产物,亲和层析纯化蛋白,酶联免疫吸附实验方法测定整合酶的生物学活性。
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Methods: With enzyme linked immunosorbent assay and micronize strengthening immunofixation, The serum OX-LDL and HS-CRP level of 215 patients with ACI was measured on the second day after hospitalization. In addition, 30 healthy volunteers were taken as the control group.
采用酶联免疫吸附试验、微粒化增强免疫固定试验测定215例ACI患者入院第2天血清中OX-LDL、HS-CRP含量水平,并与30例健康者作对照。
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On the basis of purification and immunity of vitellin, antibodies of vitellin were obtained and used to measure the concentration of vitellin in embryo in different stages of embryonic development by enzyme-linked immunosorbent assay.
在采用纯化的卵黄磷蛋白免疫兔子而获得其抗体的基础上,运用酶联免疫吸附检测法(enZyme一linked ilnlnunosorbent assay,ELISA)分析测定了发育过程中胚胎内卵黄磷蛋白的含量。
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Enzyme-linked immunosorbent assay and coagulating time method were used to assess antigenic stability and coagulating stability,respectively.
以酶联免疫吸附法测定了蛇毒降纤酶的抗原活性稳定性,并与凝固时间法测定的生物活性稳定性进行了比较。
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Enzyme-linked immuno-sorbent assay and coagulating time method were used to assess antigenic stability and coagulating stability, respectively.
以酶联免疫吸附法测定了蛇毒降纤酶的抗原活性稳定性,并与凝固时间法测定的生物活性稳定性进行了比较。
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Wistar rats were randomly divided into normal group, sham-operation group, 4 weeks diabetes mellitus model group (M4), 6 weeks diabetes mellitus model group (M6) and 8 weeks diabetes mellitus model group (M8). Behaviour was tested with Morris water maze and shuttle box test.
穿梭箱实验、Morris水迷宫实验检测大鼠认知行为学改变,免疫组织化学法、免疫印迹法、RT-PCR和酶联免疫吸附法检测BACE1;ELISA法检测Aβ在糖尿病大鼠脑组织中的表达,用图像分析仪测定吸光度值。
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