experience with 1xTAE buffer for PFGE electrophoresis!
I personally felt the difference between the use of 0.5X TBE and 1X TAE in buffer for PFGE electrophoresis was NOT SIGNIFICANT.
However mine is different I don´t know it depens on the queality of agarose or the buffer but TBE is better than TAE
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Can someone please give me some possible things that could go wrong? Here is my recipe: 0.5g Agarose 50 mL of TAE 1x 1 uL ethyl bromide. Gel was run at 100V for 1 hour. The buffer used is also TAE.
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