Hello,
I want to separate two purified proteins that have almost the same weight.
One is 16.8 kDa, the other is approx 10kDa.
I use Tris\glycine buffers.
Which gel percentage and running time should I choose?
Thank you
I would try making up a 20% gel, and running it for 60-90 minutes at a constant current https://www.novusbio.com/support/support-by-application/western-blot-sds-page
Thank you.
Can you please explain the huge overlap between the protein sizes? How can they suggest different gel percentage for proteins 4-40kD or 12-45?
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