将细胞以2,000个细胞/孔的密度接种在96孔板中,其中200μL培养基含有不同浓度的丁酸钠。然后,将细胞连续培养72小时。每24小时,将20μL5mg/ mL MTT溶液加入相应的孔中,并将细胞再培养4小时。然后,用150μL二甲基亚砜代替溶液,然后在室温下温和搅拌板15分钟。最后,测量492nm处的吸光度以代表细胞活力。
数据来源文献
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备注
以上数据均来自公开文献, Jinpan暂未进行独立验证, 仅供参考。These protocols are for reference only. Jinpan does not independently validate these methods.