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发表于 2016-9-20 18:23:14
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你要么试试下面这个方法:
Cells were counted, washed, and fixed in 70% EtOH 30% sorbitol. Samples were then treated with 1µM RNase A (Sigma, St. Louis, Missouri) in 50mM sodium citrate at 37° for 30 min., and stored at 4 C Prior to analysis, cells were stained with 1µM SYTOX Green
[文献出处:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586416/]
从图上看,效果确实很差,感觉PI这管酵母都碎了,Syto这管似乎没染好。 |
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