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Description
Suwannasom, N., Kao, I., Pru, A., Georgieva, R
Immunofluorescent staining The sections were permeabilized with 0.1% Triton X-100 in PBS for 15 min and then blocked with 5% bovine serum albumin (BSA) for 1 h at room temperature
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The proteins were incubated in following buffer conditions: Binding buffer: 20 mM TrisHCl, 200 mM NaCl, 1 mM EDTA, pH 7.4 Elution buffer: 10 mM Maltose, 20 mM TrisHCl, 200 mM NaCl, 1 mM EDTA, pH 7.4 Post-elution, the pull-down eluates were subjected to SDS-PAGE analysis keeping only MBP as the control
