I am working with some dried extract residues from protein isolation. I want to see which proteins I loose there. The protein content of these is around 25% and dry matter 93.7%. I usually use 1 mL of 1x Treatment Buffer for 50 mg protein, but in this case I would need to use 200 mg of my sample to reach the necessary protein content (50 mg). How can I change the dilution to be able to solubilize my sample but have enough protein to see in the gel?

Thank you in advance,

Veronica

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