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[求助]
篩選陽性克隆
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| 在一篇文獻上看到“cell were grown for 48h before Cm gradient was added to the media(500ul of Cm,at 10ug ml-1,was underlayed at one point of the plate perimeter and the gradient formed by diffusion through the agar)",有誰知道怎么做嗎?這樣做有什么好處,為什么不直接用5ug ml-1的抗性平板篩選呢?謝謝! |
找到一些相關的精華帖子,希望有用哦~
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