Does anyone know about how to keep DMEM (+10% FBS) media at a low pH? I tried to adjust my media at both pHs 6.5 and 5.5 by adding HCl but, few hours later (without cells) it returned close to 7 - 7.2.
Thank you all.
In our fluorescence spectrophotometer, I excited pure ethanol at 283 nm and I found a peak at 314 nm.
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