Hi all,

can you explain to me  In which conditions  it is better to choose a gradient gel instead of a normal one and why?

Also, I read on the website of some companies providing gels for protein electrophoresis that the running buffer should be chosen according to the size of the protein..For example, the MES Buffer for a separation range of 3.5 kDa to 160 kDa and MOPS buffer for  15 kDa to 260 kDa ...What does it mean? Why does the choice of the running buffer depend on the separation range of your proteins?

Thanks

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