For glycogen synthase analysis, the lysates were prepared in buffer containing of 50mMTris HCl, 10 mM EDTA, 10 mM NaCl, 50 mM NaF, 1 mM microcystin LR, 1% Nonidet P 40 and 1% protease inhibitor cocktail. The cells were scraped, collected within an eppendorf and permitted to stand on ice for 30 min. The lysates
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