Production of L - [ 3 H ] citrulline from L - [ 3 H ] arginine was measured to determine eNOS activity.
37℃暴露5min后 测定L - [ 3H ] 精氨酸产生的L - [ 3H ] 瓜氨酸量来反映eNOS活性.
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AIM To detemine absorption and absolute bioavilability of [ 3 H ] lofexidine ( LOF ) in rats.
目的 研究了 [ 3H ] 洛非西定的吸收和绝对生物利用度.
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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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To patients with cerebral vasospasm after operation we gived 3 H therapy.
术后出现脑血管痉挛的患者使用3H疗法治疗.
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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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H - NSP is current important reagent for introduction of tritium into proteins and polypeptide.
~3H-NSP是目前将氚引入到蛋白质和多肽的一种重要试剂.
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CINC proteins in SAP group were detected in alveolar cells from 3 h after operation.
SAP组术后3h肺泡细胞有CINC蛋白 的表达.
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While in DCB method, the highest yield was 99 %, which was achieved by THF after 3 h.
在DCB法中, 使用弱极性溶剂THF时,反应3h,连接率可达99%.
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Conclusion Using narceine and 3 H therapy is effective for patients cerebral vasospasm after ruptured aneurysm.
结论应用罂粟碱和3H疗法是治疗脑动脉瘤破裂后迟发脑血管痉挛的一种有效的方法.
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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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DNA and protein synthesis was detected by [ 3 H ] thymidine as well as [ 3 H ] TdR incorporation , respectively.
[3H]亮氨酸掺入法及 [ 3H ] 胸腺嘧啶核苷掺入法检测细胞内蛋白、DNA合成.
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The difference in their DNA synthesis inhibition rate and radiosensitivity were expressed by tritium incorporation method.
用3H掺入法说明DNA合成抑制率与放射敏感性的不同.
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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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