AT - 1420 significantly inhibited tne incorporation of 3 H - TdR into EAC cells.

另口服和注射给药均有效.AT -1420 对~3H-TdR参入EAC细胞中有明显的抑制作用,抑制率为70%(±8.1).

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LTT was assayed by 3 H - TdR incorporation method.

外周血淋巴细胞转化率测定采用3H - TdR渗入法.

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Results: LPA enhanced the cultured VSMC ? 3 H ? TdR incorporation in a concentration? dependent manner, and increased MAPK activity concurrently.

结果: LPA呈浓度依赖地刺激3H? TdR参入, 并平行地激活MAPK,二者间呈显著正相关.

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Tritium labeled thymine deoxyriboside ( [ 3 H ] TdR ) uptake was measured to observe DNA synthesis.

氚胸腺嘧啶核苷 ( [ 3H ] TdR ) 掺入法检测TP40对T24细胞蛋白质合成的抑制作用.

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Except for ￣3 H - Pro , no significant differences in the incorporation of ￣3 H - TdR and ￣14 C - UR in Fbsbetween VO and SO groups.

除~3H - Pto外,VO组的~3H - TdR及 ~14C-UR掺入率与SO组相比差异无显著性.

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The AFP concentration was determinated with radioimmunoassay, while the DNA synthesis was studied by the 3 H - TdR incorporation ( CPM ).

放射免疫法检测肝癌细胞分泌甲胎蛋白(AFP) 含量,3H - TdR掺入法测定DNA合成放射活性 ( CPM ).

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The combo of 3 H - thymidine ( 3 H - TdR ) and H 235 SO 4 were used to detect radiolabeled DNA and proteoglycan syntheses, respectively.

振动培养后的 3H-TdR 和H235SO4的结合物分别被用于检测已标志的DNA和蛋白聚糖合成.

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The incorporation of 3 H - TdR was determined to identify the best antigen induce dose.

确定最佳的HCV抗原 诱导剂量. 实验采用~3H-TdR掺入法.

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The labelling of 3 H TdR was heterogenous, being distinct on the endings of glandular ducts.

结果显示:3H?TdR标记呈不均一性,腺管末梢标记明显.

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