大家好,
请问如果流式染色结束后不能及时上机应该如何操作?听说可以用PFA固定,请问是一直泡在PFA里,等要上机了直接用吗?
因为在Biolegend的官网上看的protocol里这样写:
Perform fluorescence activated cell sorting (FACS), or flow cytometric analysis.
Note: If you are unable to immediately read your samples on a cytometer, keep them shielded from light and in a refrigerator set at 4-8°C. The samples should be resuspended in Cell Staining Buffer. Note that samples should not remain in a fixation buffer for extended periods of time as this can affect fluor conformation and fluorescence. 他这里的cell staining buffer就是类似PBS而已,所以我很疑惑难道不应该重悬再PFA里吗?
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