Most proteins at the plasma membrane are not uniformly distributed but localize to dynamic domains of nanoscale dimensions. To investigate their functional relevance, there is a need for methods that
A row of large IMPs bordering parts of the plates are visible. Two parentheses-shaped empty trichocyst docking sites are also present and one ring surrounding pits where the rosette IMPs have been rem
Proteomics analysis of membrane proteins extracted from iPS spheres. Membrane fractions were isolated, treated with 8 M urea, and trypsinized. The peptides were fractionated (4 fractions) and analyzed
