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?