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Herein we explain a robust solution to integrate recombinantly created full-length caveolin-1 into bicelles at levels needed for biophysical experimentation. The standard of effective reconstitution may be the obtainment of protein in a homogeneous condition; consequently, we developed a validation process observe the success of the reconstitution utilizing analytical ultracentrifugation of density-matched bicelles. Our results suggested which our protocol creates a tremendously homogen
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