Hello, all

I am currently extracting LPS from E. coli MG1655 and its mutant strains.

I followed several different protocols (phenol methods or phenol+diethy ether methods), but I couldn't see the ladder pattern of LPS. What I can see clear is the fat band at the bottom of SDS-PAGE (probably lipid A part?)

Can anyone give me suggestions? Is culture condition or pH important? Is LPS degraded during prep?

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