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For animal experiments, is a DMSO concentration of 10% or 5% more appropriate for rat liver tissue cryopreservation solution?

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Asked by:Bio 2026-04-24 Views 269 4 answers
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All Answers4
宋
宋磊强6787 2026-09-22
如果下游要做石蜡切片或HE/免疫组化,DMSO残留可能影响固定和染色质量。冻存组织复苏后建议用含10%~20%血清的培养基或预冷PBS充分洗涤,再进行固定或下游实验。配冻存液时血清和DMSO混合会放热,需要在冰上缓慢加DMSO,避免局部高温损伤蛋白。10% DMSO本身不是影响病理的唯一因素,冻存前取材、切片厚度和程序降温也会影响结果。
L
Lily 2026-09-16
组织冻存用量一般不大,建议买50~100mL细胞培养级DMSO,性价比比500mL大瓶更合适。大瓶虽然单价低,但冻存液用量少,开封后吸潮和污染风险会抵消价差。小包装到货后可直接分装成2~5mL无菌冻存管,每管对应一次实验。比价时按实际可用mL数算,把分装耗材、手套箱或干燥保存成本也考虑进去。
B
Bioer 2026-09-13
肝组织冻存用10% DMSO加含血清培养基更常见,尤其大鼠肝组织块较大,5% DMSO可能渗透和抗冰晶能力不足。如果担心10%对病理切片影响,建议把肝切成1~2mm厚的小条,保证冻存液渗透,复苏后立即用预冷PBS或培养基洗2~3次再固定。也可同一批样本分5%和10%两组对比,看细胞核形态和冰晶空泡,用数据决定,不要凭经验一刀切。
E
Emma 2026-07-07
DMSO吸潮确实是常见问题,开封后接触空气会吸水和氧化,长期开口瓶可能颜色变深、水分升高。建议到货后在干燥环境中分装,动作快一些;分装后拧紧密闭,放干燥器或阴凉处。DMSO在18℃左右会凝固,放冰箱后取用需室温融化,反复冻融会让管壁产生冷凝水,所以更应分装小管,不要整瓶反复冻融。
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