My protein is 25KD and its pI is 5.5. How much concentration of my native page could be? The native page could deter the tiny mobility changes? And which is the right running buffer, 0.5*TBE or Tris-Glycine?
Thanks.
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Hello! I'll do a size exclusion chromatography, but I only have an open column, and I'll perform the peptide extraction from yeast, using buffer lysis (sodium phosphate 50 mM/NaCl 30 mM/DNAse and...
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