氯化亚汞

2 The analysis step by 25.0mL sample lixivium, moved in the direction of arsenic in the bottle, plus 10 ml of hydrochloric acid and 10 ml of potassium iodide solution and 5 drop acid stannochlor solution, shake the place 10min, together with 2 g of arsenic-free zinc metal, immediately mounted a good lead acetate paper turns red cotton and mercury bromide from log that arsenic tube placed in the 25-38, f μh of the dark side, remove the test strip and standard mercury bromide a color not deeper than standard.

7.2 分析步骤取25.0mL样品浸泡液，移入测砷瓶中，加5mL盐酸、5mL碘化钾溶液及5滴酸性氯化亚锡溶液，摇匀后放置10min，加2g无砷金属锌，立即将已装好乙酸铅棉花及溴化汞试纸的测砷管装上，放置于25～30℃的暗处1h，取出溴化汞试纸和标准比较，其色斑不得深于标准。

Methods Vero cells were cultured with mercury chloride, at the same time zinc sulfate, sodium selenite and zinc sulfate together with sodium selenite were added respectively. The tail length and the rate of the comet cells were measured and calculated.

常规培养vero细胞，通过MTT法制定出氯化汞染毒剂量，与氯化汞同时加入不同浓度的硫酸锌、亚硒酸钠以及硫酸锌+亚硒酸钠溶液，共同培养2 h后采用单细胞凝胶电泳法检测细胞的彗星尾长和彗星率。

Result zinc sulfate, sodium selenite and zinc sulfate together with sodium selenite had the effects of antagonism to DNA amage caused by mercury chloride in vero cells.

结果 硫酸锌和亚硒酸钠，以及两者合用都具有拮抗氯化汞致vero细胞DNA损伤的作用，两者最佳组合是1.5 mg/L硫酸锌+1.0μmol/L亚硒酸钠。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。