Buffer question

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Frank Hardy

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For those of you who use it- is TAE (Tris acetate EDTA) for DNA gels pH'd to 8.0 or 8.5? Need to know ASAP. Thanks!
 
Hard24Get said:

Usually 8.0 but you can prepare the buffer with slightly lower or higher pH by adding either acid or base.
 
Thanks.

I already made it with 8.0. I don't think it's critical.
 
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