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assays相关的网络例句

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与 assays 相关的网络例句 [注:此内容来源于网络,仅供参考]

Or utilize both the syringe and peristaltic pumps for more complex 'hybrid' assays.

FIAlab运用了注射针及蠕动泵浦用於更复杂的&hybrid&分析模式。

Since the relative antioxidant capacity of all the phenolic compounds was much higher than trolox in both assays, it is a good indication that phenolic compounds possess high antioxidation capacity against peroxy radicals.

由於酚类物质之相对抗氧化力均远高於trolox,表示酚类物质对过氧自由基具有很好的抗氧化效果。

Antioxidant activity of Se-PC was investigated and compared with phycocyanin by using four different free radical scavenging assays, namely, trolox equivalent antioxidant capacity assay, DPPH free radical scavenging assay, superoxide anion scavenging assay and assay for erythrocyte hemolysis mediated by peroxyl free radicals .

通过含硒藻蓝蛋白与藻蓝蛋白对4种不同的自由基清除能力的比较,即总抗氧化能力、清除DPPH自由基、过氧化物阴离子和引发红细胞溶血的过氧化氢自由基能力测定,从而对含硒藻蓝蛋白的抗氧化活性进行评价。

These assays can be easily adapted to other pharmacologically relevant receptors .

这些测定可以被简单的应用到药理学有关的方面。

Thus, many monographs for Pharmacopeial preparations feature chromatographic assays.

因此,许多有关药典制剂专论中特别说明了色谱分析。

This value represents the maximum allowable impact from this source of variation, when taken with the variation allowed by the composite of other Pharmacopeial tests and assays for both the bulk pharmaceutical chemical and the preparations.

该数值代表该变异来源允许的最大值,此时考虑了其他散装化学药品和制剂的药典检查和分析一起允许的差异。

Reverse-transcription PCR assays were used to detect the mRNA expression level of related regulatory genes such as p15, p16, p21, p27, p57, surviving, cyclin B, cdc2 and chk1, and Western blot assay to detect the level of protein expression and phosphated change such as survivin, cdc2 and chk1. Results:(1) K562 cell arrested on G2/M phase were obviously increased after co-cultured with 2 to 10μmol/L Arsenic trioxide for 24 hours. The ratios of control group, 2μmol/L, 5μmol/L and 10μmol/L groups were 22.6±3.4%, 27.2±2.3%, 43.8±4.5% and 36.7±4.1%, respectively.

体外培养K562细胞,以不同浓度AS_2O_3作用不同时间后采用PI染色、流式细胞仪检测药物作用后细胞的周期分布改变;逆转录酶多聚酶链扩增方法检测细胞周期相关调节基因(p15、p16、p21、p27、p57、survivin、cyclinB、cdc2、chk1)的mRNA表达变化;Western blot方法检测细胞周期相关调节蛋白表达及磷酸化改变(survivin、cdc2、cdc2-p、chk1)。

PPARα ligands suppressed OPN promoter actiity, and an actiator protein-1 consensus site conferred this repression. Oerexpression of c-Fos and c-Jun reersed the inhibitory effect of PPARα ligands on OPN transcription, and, in chromatin immunoprecipitation assays, PPARα ligands inhibited c-Fos and phospho–c-Jun binding to the OPN promoter.

PPARα配体可抑制OPN启动子活性,一个激活蛋白-1的一致序列位点与这种抑制有关。c-Fos和c-Jun的过表达可逆转 PPARα配体对OPN转录的抑制作用,并且在免疫沉淀实验中,PPARα配体可抑制c-Fos及磷酸化c-Jun与OPN启动子的结合。

Complementation assays in planta showed that either the deletion in the lipoprotein domain or in the transmembrane domain did not restore HR induction in tobacco and pathogenicity in rice to the hrcJ mutant.

功能互补结果显示,缺失脂蛋白结构域和跨膜结构域的hrcJ基因均不能恢复hrcJ突变体在烟草上的HR激发能力和在水稻上的致病性。

The software also supports gene expression analysis of data produced using commercial assays, including QuantiGene Plex kits, automatic outlier detection based on standard deviation within a replicate group, and support for customizable reports.

这套软件还支持使用商业检测方法获得的基因表达分析,包括QuantiGene Plex试剂盒、根据重复组标准差自动进行的无关项检测,并支持进行拥护自定义的报告。

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