割引で80%オフ
The corresponding amount of lipid was dissolved in chloroform, and then the solvent was removed under N 2 stream to obtain a lipid film. The lipid films were hydrated for 30 min in buffer (20 mM HEPES, pH 7.4 for E. coli or Hepes 20 mM, NaCl 500 mM, and EDTA 1 mM pH 7.4 for S. aureus ) in a sonicator at 37 °C.
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