This work explores methods for forming and characterizing biomimetic planar membranes composed of amphiphilic block copolymers. The membranes are diblocks and triblocks with hydrophilic blocks of poly(2-methy1-2oxazoline), (PMOXA) and hydrophobic blocks of poly(dimethylsiloxane) (PDMS). Experiments with the lipid diphytanoyl phosphocholine (DPhPC) serve as a basis for comparison with the polymeric membranes. Phase-contrast microscopy is used to study how membranes evolve over time after their formation. Capacitance measurements as a function of the thinned membrane area (prepared from two separate solvent systems) are performed to clarify the importance of the Plateau Gibbs border in electrical measurements. Finally, functional reconstitution of the two ion channels, alamethicin and gramicidin, is investigated. Imaging in transmitted phase-contrast mode provides visualization of thinned regions that contain monolayers or bilayers (in the case of diblock copolymer). The specific capacitance measurements yield 0.28 mu Ficm2 with a corresponding thickness of 8.5 nm for PMOXA(6-)PDMS(35)-PMOXA(6) (blocks of 6 PMOXA and 35 PDMS repeat units) formed from a solution of ethanol decane, 0.55 mu F/cm' and 4.4 nm in chloroform toluene, and 0.46 mu F/cm(2) and 5.4 nm for the diblock PMOXA(6)-PDMS17, in ethanol decane. Alamethicin reconstitution in the block copolymers shows slower channel forming kinetics with somewhat higher conductance values than found in DPhPC. Gramicidin in the block copolymer shows a slightly voltage-dependent conductance as a function of time, with little stochastic conductance state switching, in contrast to reconstitution in DPhPC where gramicidin switches states at similar to 3 Hz.