You may collect the C. albicans cells in a test tube. Wash the cells adequately twice with 0.05 M phosphate buffer pH 6.5 and directly lyse/ homogenize the cells in SDS-PAGE buffer. Heat for 3-4 min in boiling water bath, centrifuge the cells debris and use the supernatant to load on SDS-PAGE, and thence perform WB.
Shamsher S. Kanwar what is mean "lyse/ homogenize the cells in SDS-PAGE buffer."? how i can lysis with this buffer, and what is the percentage of the SDS-page buffer?
Simply use sample buffer (Tris buffer pH 6.8 containing 30% Glycerol, 1% SDS, mercaptoethanol and bromophenol blue) + C. albicans cell + glass or zircon beads in a pestle motar or homogenizer. Rupture cell, centrifuge suspension at 10000 g for 10 min at 4c and load supernatant on SDS PAGE.