b subunits, b+7-his and bA7-HA, did not dimerize. Similar experiments were performed with a seven amino acid size difference as opposed to the fourteen amino acid difference just attempted (data not shown). The immunoblot analysis gave identical results to the previous data, b+7-his and bwt-HA dimerization was not detected, suggesting the two different b subunits had incorporated into F1Fo ATP synthase in a segregated manner. However, further experimentation utilizing this experimental approach indicated that dimerization was not detected between two wild type length b subunits, bwt-his and bwt-HA, Mern brane prep. Ni-Resin Purified -- -+ -- Ar a nti-br 2 a nti-HA -i I +bH Fiue -. irei u rfctoofitdnanHAeioetgeFIoraedwhte crs-ine S3 rdemmraepeartos fK 2 xrssn h difrn uuis eecoslne (aeil n ehos.Tepout weete ouiie n ujce oNirsnprfcto eoesprto usnga at-H ouemooloa atboy